<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">Health</journal-id><journal-title-group><journal-title>Health</journal-title></journal-title-group><issn pub-type="epub">1949-4998</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/health.2019.117078</article-id><article-id pub-id-type="publisher-id">Health-94010</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject><subject> Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Naturally Derived Formulations and Prospects towards Cancer
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Neha</surname><given-names>Masarkar</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Sukhes</surname><given-names>Mukherjee</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Sudhir</surname><given-names>K. Goel</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Rajeev</surname><given-names>Nema</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>All India Institute of Medical Science (AIIMS), Bhopal (Madhya Pradesh), India</addr-line></aff><pub-date pub-type="epub"><day>03</day><month>07</month><year>2019</year></pub-date><volume>11</volume><issue>07</issue><fpage>971</fpage><lpage>997</lpage><history><date date-type="received"><day>28,</day>	<month>February</month>	<year>2019</year></date><date date-type="rev-recd"><day>27,</day>	<month>July</month>	<year>2019</year>	</date><date date-type="accepted"><day>30,</day>	<month>July</month>	<year>2019</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Traditional Medicine (TM) and their secondary metabolites are being increasingly recognized as useful complementary treatments toward the cancer. A large number of clinical studies have reported and proven concern of cancer patients. Here we have also reported recent studies on the biochemical and cellular mechanisms of Traditional Medicine (TM). Nowadays, Chemotherapy and surgery are standard methods for treatment of cancer, but still it’s not been fully successful. Some progress has been made in cancer diagnosis and treatment, but high incidence rate of cancer and low survival rate of patient are still being reported worldwide. Since ancient times, a number of traditional medicines known as Ayurveda, Siddha, Unani, Iranian, Chinese, Korean, acupuncture, Muti, Ifa, and African medicine are widely used for therapeutic purposes and are becoming popular as Traditional Medicine (TM). It has been reported that plants synthesize plethora of “secondary metabolites” or “phytochemicals”, proven to possess anti-mutagenic and anti-cancer properties in many research studies. There are many possibilities for further organized research for screening of medicinal plants for their potential and efficacy against chronic diseases such as a cancer and other inflammatory diseases. Therefore, researcher’s interest should be in identification and standardization of new anti-cancer drug with low side effects and greater efficacy, that is easily acceptable in medical community and which may overcome the challenges in present and future cancer therapy. This review explores therapeutic value of certain bio-active principals of plant which could serve as potential pharmacologically active drug for treatment of cancer in future.
 
</p></abstract><kwd-group><kwd>Bio-Active Principles</kwd><kwd> Cancer</kwd><kwd> Chemotherapy</kwd><kwd> Phytochemicals</kwd><kwd> Secondary Metabolites</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><sec id="s1_1"><title>1.1. Conventional Cancer Therapy</title><p>Cancer is a state which arises when cells start dividing in an uncontrolled manner disobeying the check mechanisms, which controls the rate of cell proliferation leading to the formation of a neoplastic tumor, which may be benign or malignant. Cancer arises mainly due to two reasons: one is Gain of function of a proto-oncogene, which makes it oncogenic and second is Loss of function of a tumor suppressor gene [<xref ref-type="bibr" rid="scirp.94010-ref1">1</xref>] . Despite the latest advancements in the cancer treatment it remains a key cause of death worldwide [<xref ref-type="bibr" rid="scirp.94010-ref2">2</xref>] . Current treatment includes chemotherapy, radiations and surgery, out of which chemotherapy is most common. Most successful chemotherapeutic agents include: Taxanes-paclitaxel (Taxol), docetaxel (Taxotere), albumin bound paclitaxel (Abraxane), Anthracyclines-doxorubicin, pegylated liposomal doxorubicin, epirubicin, Platinum agents-cisplastin, carboplastin etc. All these agents cause serious side effects [<xref ref-type="bibr" rid="scirp.94010-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref5">5</xref>] , which includes kidney, liver, nerve and blood vessel damage, hearing loss, lower blood count etc. [<xref ref-type="bibr" rid="scirp.94010-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref7">7</xref>] , regional toxicity affecting mucosa cells, causing irritative urinary and blood loss [<xref ref-type="bibr" rid="scirp.94010-ref7">7</xref>] . Later toxic effects include damage to proliferating cells such as fibroblasts, endothelial and parenchymal cells [<xref ref-type="bibr" rid="scirp.94010-ref7">7</xref>] . Other undesired side effects such as immune suppression, bone necrosis, lung fibrosis and skin devascularization are seen with all conventional therapies [<xref ref-type="bibr" rid="scirp.94010-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref8">8</xref>] . Although the desired goal of chemotherapy is to eliminate the tumor cells, diverse range of normal cells is also affected, leading to many adverse side effects on multiple organ systems [<xref ref-type="bibr" rid="scirp.94010-ref9">9</xref>] - [<xref ref-type="bibr" rid="scirp.94010-ref14">14</xref>] . Such debilitating effects and toxicity are a major clinical problem which limits the usefulness of anticancer agents [<xref ref-type="bibr" rid="scirp.94010-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref16">16</xref>] . Knowing how the chemotherapeutic agents work is important in predicting its side effects. For instance, treatment with alkylating agents and topoisomerase II inhibitors increases the risk of secondary cancer (acute leukaemia); anthracyclines (like doxorubicin) induce cardiotoxicity; and mitotic inhibitors have the potential to cause peripheral nerve damage [<xref ref-type="bibr" rid="scirp.94010-ref17">17</xref>] . Over 75% of cancer patients suffer from therapy associated fatigue, nausea, vomiting, pain, rashes, infection, headaches, which considerably decreases the quality life of the patients [<xref ref-type="bibr" rid="scirp.94010-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref19">19</xref>] . They also affect the nutritional status of the patients [<xref ref-type="bibr" rid="scirp.94010-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref18">18</xref>] causing malnutrition, which is one of the major reasons why cancer patients die [<xref ref-type="bibr" rid="scirp.94010-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref18">18</xref>] . Ongoing researches on several secondary metabolites are under clinical trials for the treatment of various diseases including cancer. TM/CAM and its derived compounds are an essential aspect for therapeutics, and nano-particles based approaches could be a new hope for additional therapy for cancer treatment [<xref ref-type="bibr" rid="scirp.94010-ref20">20</xref>] .</p></sec><sec id="s1_2"><title>1.2. Ancient History of Traditional Medicine</title><p>From ancient times, traditional medicinal plants are being used for treatment of various diseases [<xref ref-type="bibr" rid="scirp.94010-ref21">21</xref>] . Natural medicine sometimes referred to as herbalism or botanical medicine is the use of plants for their therapeutic or medicinal value and has been used by many cultures throughout history [<xref ref-type="bibr" rid="scirp.94010-ref22">22</xref>] . The oldest written facts about medicinal plants and the uses of plants are contained in thousands of poetic hymns in the Rig Veda. The first school to teach Ayurvedic medicine was at the University of Banaras in 500 BC where the great Samhita (or encyclopedia of medicine) was written. Another great enclyclopedia was written 700 years later, and these two together forms the basis of the Ayurveda or Indian medicinal plant concept [<xref ref-type="bibr" rid="scirp.94010-ref23">23</xref>] . The different indigenous system of medicine namely Ayurveda, Siddha, Unani, Iranian, Chinese, Korean, acupuncture, Muti, Ifa, and African medicine have been in existence and used in several countries for treatment. These systems of medicine provide to the needs of nearly 70% of the population residing in the villages. Apart from India, these systems of medicine are prevalent in China, Korea, Middle Eastern, European, Africa and America and many other countries [<xref ref-type="bibr" rid="scirp.94010-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref25">25</xref>] . India has a rich culture of using medicinal herbs and spices, which includes about more than 2000 species and has a vast geographical area with high potential abilities to be used as traditional medicines but only very few have been considered chemically and pharmacologically for their prospective medicinal value [<xref ref-type="bibr" rid="scirp.94010-ref26">26</xref>] . In 1819, morphine, codeine and paregoric acid were isolated which laid down the foundation for isolation of pharmacologically active compounds. Even today, morphine remains the standard for measuring synthetic analgesic drugs. In addition U.S. based research has proved the medicinal properties of alkaloids from Madagascar periwinkle (Catharanthus roseus), used in the chemotherapy of childhood leukemia and for the treatment of Hodgkin’s disease (Taxus brevifolia), and approved by FDA in 1992. As per our recent knowledge about 25% to 30% of the prescribed drug contains at-least one or two active ingredients derived from plants [<xref ref-type="bibr" rid="scirp.94010-ref27">27</xref>] . Many drugs listed as conventional medications were originally derived from plants [<xref ref-type="bibr" rid="scirp.94010-ref28">28</xref>] . Salicylic acid, a precursor of aspirin, was originally derived from “white willow bark” and “meadowsweet plant” [<xref ref-type="bibr" rid="scirp.94010-ref29">29</xref>] . Other plant derived drugs include the anti-malarial “quinine” extracted from the bark of Cinchona species. “Vincristine” used in cancer treatment is derived from “Madagascar periwinkle” (Catharanthus roseus) [<xref ref-type="bibr" rid="scirp.94010-ref30">30</xref>] .</p></sec><sec id="s1_3"><title>1.3. Traditional Medicine</title><p>The use of traditional medicine (TM) and complementary and alternative medicine (CAM) as therapeutics is growing all over the world [<xref ref-type="bibr" rid="scirp.94010-ref31">31</xref>] . Already, it accounts for a major part of the health care provided worldwide. In low- and middle-income countries, up to 80% of the population relies on TM for their primary health care needs [<xref ref-type="bibr" rid="scirp.94010-ref32">32</xref>] . In many high income countries CAM utilization is becoming increasingly popular, with up to 65% of the population reported that they have used this form of medicine [<xref ref-type="bibr" rid="scirp.94010-ref32">32</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref33">33</xref>] . Today plant based drugs play an essential role in health care. According to WHO, 80% of the world population rely on traditional medicines for primary health care [<xref ref-type="bibr" rid="scirp.94010-ref34">34</xref>] . Currently 119 chemicals derived from 90 plant species constitute major drugs. Studies showed that plant derived drugs represent about 25% of the American drug market [<xref ref-type="bibr" rid="scirp.94010-ref35">35</xref>] . There are more than 250,000 plant species in world with unique secondary constituents [<xref ref-type="bibr" rid="scirp.94010-ref36">36</xref>] , however, only few of them have been investigated for their potential value as a drug. Furthermore, medicinal plants typically contain mixtures of different phytochemicals that may act individually, additively or in synergy to improve health [<xref ref-type="bibr" rid="scirp.94010-ref37">37</xref>] and enhance mood and give a sense of well-being [<xref ref-type="bibr" rid="scirp.94010-ref38">38</xref>] . Now we have enough scientific reasons for using TM/CAM as a more effective therapy in comparison to conventional medicines. Apart from therapy some Indian and African communities, traditional medicines are thought to help clean out negative spiritual influences [<xref ref-type="bibr" rid="scirp.94010-ref39">39</xref>] and supporters of TM/CAM use them frequently as they are generally safe at common doses [<xref ref-type="bibr" rid="scirp.94010-ref40">40</xref>] . More than 3000 plants based secondary metabolite worldwide have been clinically reported to have anticancer properties [<xref ref-type="bibr" rid="scirp.94010-ref41">41</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref42">42</xref>] . TM/CAM medicine use is still common in oncology therapy worldwide [<xref ref-type="bibr" rid="scirp.94010-ref43">43</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref44">44</xref>] . In the last two decades, the use of herbal remedies has also been widely increased in many developed countries as TM/CAM. Secondary metabolite have increasing attention in cancer chemotherapy because they are viewed as more biologically active target sites and are less toxic to normal cells [<xref ref-type="bibr" rid="scirp.94010-ref45">45</xref>] . Moreover, there is evidence that natural product-derived anticancer drugs have alternative modes of promoting cell death [<xref ref-type="bibr" rid="scirp.94010-ref46">46</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref47">47</xref>] . In fact, the use of TM/CAM based metabolite as the background to discover and develop a drug entity is still a research attention.</p></sec><sec id="s1_4"><title>1.4. WHO Traditional Medicine Strategy</title><p>According to WHO definition of traditional medicine (TM) is as follows “Diverse health practices, approaches, knowledge, beliefs incorporating plant, animal, and/or mineral based medicines, spiritual therapies, manual techniques and exercises applied singularly or in combination to maintain well-being, as well as to treat, diagnose or prevent illness” [<xref ref-type="bibr" rid="scirp.94010-ref48">48</xref>] . TM is a comprehensive word used to refer many systems of traditional medicine and other various forms of local medicines.</p><p>In developed and developing countries where the dominant health care systems look forward on allopathic medicine, apart from conventional approach now scientist are thinking toward traditional medicine (TM) and these medicine often termed as “complementary’ alternative” or “non-conventional” medicine. Herbal medicine includes herbs and plant active ingredients or plant secondary metabolites. In addition general sense to all above mentioned regions for Traditional Medicine/Complementary alternative medicine (TM/CAM) is still in used [<xref ref-type="bibr" rid="scirp.94010-ref48">48</xref>] for their healthcare purposes. In many parts of the world expenditure on TM/CAM is increasing rapidly. The mission of WHO for essential drugs and medicine policy is that: it helps to save lives and improve healthcare facilities by healing the huge gap between the potential that essential drugs have to offer towards patient care patients care. In most developing countries, national TM/CAM institutes have been established, like in India, China, North and South Korea, Ghana, Indonesia, Mali, Madagascar, Nigeria, Sri Lanka, Thailand, Vietnam and list goes on. In addition WHO also provides guidelines, scientific information and research grant into the safety and efficacy of use of TM/CAM.</p><p>According to WHO TM strategy, the functions of WHO in TM/CAM can be outlined as follows (WHO traditional medicine strategy: 2014-2023):</p><p>&#183; Facilitating integration of TM/CAM into national healthcare systems by helping member states to develop their own national policies on TM/CAM.</p><p>&#183; Producing guidelines for TM/CAM by developing and providing international standards, technical guidelines, and methodologies for research into TM/CAM therapies and products, and for use during manufacture.</p><p>&#183; Stimulating strategic research into TM/CAM by providing support for clinical research projects on safety and efficacy of TM/CAM, particularly with references to diseases such as malaria and HIV/AIDS.</p><p>&#183; Advocating the rational use of TM/CAM by promoting evidence based TM/CAM.</p><p>&#183; Managing information on TM/CAM by acting as a clearing house to facilitate information exchange on TM/CAM.</p></sec><sec id="s1_5"><title>1.5. Formulation Development and Discovery</title><p>Discovery of TM/CAM drugs has become one of the main areas of interest in pharmacological research [<xref ref-type="bibr" rid="scirp.94010-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref45">45</xref>] During the last few years, the development of active compounds (plant secondary metabolites) based drugs has risen significantly, this can, in part, be attributed to the new technologies in natural product isolation and purification, combinatorial synthesis and high-throughput screening [<xref ref-type="bibr" rid="scirp.94010-ref49">49</xref>] . Natural products from dietary components such as Indian spices and medicinal plants are known to possess antioxidant activity. Recently, more than 100 new active compounds have been isolated as anti-cancer agents from plant sources [<xref ref-type="bibr" rid="scirp.94010-ref1">1</xref>] . Drug development is an essential part of research owing to low bio-availability of flavonoids and their lack of stability, excessive metabolism, permeability problems, lack of site specificity in distribution, rapid elimination etc. The scope of this review is to assess and put into perspective salient features of some recently reported work on Plant secondary metabolites including the methylated compounds that showed improved drug like properties [<xref ref-type="bibr" rid="scirp.94010-ref50">50</xref>] . Nowadays a number of approaches are being considered for selecting higher plants as reference for anti cancer drug development with the aim of drug accomplishment, and to highlight the role of ethno medicine [<xref ref-type="bibr" rid="scirp.94010-ref51">51</xref>] . During the last few decades, a wide range of anti-cancer agents were discovered from plants, but only a few of them managed to reach clinical use, from their successful chemical identification, to their effectiveness in therapeutic cancer treatment. Each of them has their advantages and limitations. Few of them approved by FDA are Vincristine [<xref ref-type="bibr" rid="scirp.94010-ref52">52</xref>] , Paclitaxel [<xref ref-type="bibr" rid="scirp.94010-ref53">53</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref54">54</xref>] , Homoharringtonine [<xref ref-type="bibr" rid="scirp.94010-ref55">55</xref>] , Curcumin [<xref ref-type="bibr" rid="scirp.94010-ref56">56</xref>] and Betulinic Acid [<xref ref-type="bibr" rid="scirp.94010-ref57">57</xref>] . All of them are derived from natural products [<xref ref-type="bibr" rid="scirp.94010-ref58">58</xref>] .</p></sec><sec id="s1_6"><title>1.6. Active Secondary Metabolites</title><p>Phytochemicals (plant secondary metabolites) are bioactive substances or active ingredients of plants which are responsible for its biological and medicinal properties [<xref ref-type="bibr" rid="scirp.94010-ref59">59</xref>] . They have found to be associated in the protection of humans against chronic degenerative diseases [<xref ref-type="bibr" rid="scirp.94010-ref60">60</xref>] . The term “Phytochemical” according to American Cancer Society refers to a wide variety of compounds produced by plants and can be found in fruits, vegetables, beans, grains etc. The isolated active compounds from these plants are used for applied research. Some of the plant chemicals are: flavonoids, alkaloids, saponins, tannins, cardiac glycosides, antharquinones, sterols and triterpenes etc. [<xref ref-type="bibr" rid="scirp.94010-ref61">61</xref>] .</p><p>&#183; Flavonoids: Flavonoids are water soluble polyphenolic molecules containing 15 carbon atoms and is the most studied phytochemical. They can be visualized as two benzene rings which are joined together with a three carbon chain. One of the carbons of the short chain is always connected to a carbon of one of the benzene rings, either directly or through an oxygen bridge, thereby forming a third middle ring [<xref ref-type="bibr" rid="scirp.94010-ref62">62</xref>] . They can be classified into six major sub-groups: flavones, flavonols, flavanones, catechins, anthocyanidins and isoflavones [<xref ref-type="bibr" rid="scirp.94010-ref63">63</xref>] . Quercetin, is one of the best described of this group. It is found in abundance in onions, apples, broccoli and berries. Flavonoid is involved in the scavenging of oxygen derived free radicals [<xref ref-type="bibr" rid="scirp.94010-ref63">63</xref>] , and is also a potent hypolipidemic agent [<xref ref-type="bibr" rid="scirp.94010-ref64">64</xref>] . They possess a high antioxidant potential due to their hydroxyl groups and protect efficiently against diseases like arteriosclerosis [<xref ref-type="bibr" rid="scirp.94010-ref65">65</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref66">66</xref>] . Experimental studies showed that flavonoids enhance vaso-relaxant process [<xref ref-type="bibr" rid="scirp.94010-ref67">67</xref>] and prevent platelet related thrombosis [<xref ref-type="bibr" rid="scirp.94010-ref68">68</xref>] .</p><p>&#183; Saponins: They are naturally occurring surface glycosides. They are synthesized by plants, some bacteria and lower marine animals [<xref ref-type="bibr" rid="scirp.94010-ref69">69</xref>] . Saponins derived its name from its ability to form soap like foams in aqueous solutions [<xref ref-type="bibr" rid="scirp.94010-ref70">70</xref>] . The structure of saponin consists of a sugar moiety (glucose, galactose, glucuronic acid, xylose, rhamnose or methyl pentose) which is linked via glycosidic linkage and attached to a hydrophobic aglycone (sapogenin) which may be a triterpenoid or a steroid. Two types of saponin have been identified, the triterpenoid and steroid saponins. The steroid saponins are often found in medicinal plants, oats, capsicum, pepper, aubergine and ginseng. Triterpenenoid saponins can be found in many legumes such as soyabeans, beans, peas, lurcene etc. [<xref ref-type="bibr" rid="scirp.94010-ref71">71</xref>] . Both triterpene and steroidal aglycones have a number of different substituents (H, COOH, and CH<sub>3</sub>). The sugars can be attached to the aglycone either as one, two or three side chains [<xref ref-type="bibr" rid="scirp.94010-ref72">72</xref>] . Saponin exhibits anti-microbial activity and has a lytic effect on erythrocyte membrane [<xref ref-type="bibr" rid="scirp.94010-ref73">73</xref>] . It has also demonstrated hypoglycemic effect [<xref ref-type="bibr" rid="scirp.94010-ref74">74</xref>] and lowering of serum cholesterol levels in animals [<xref ref-type="bibr" rid="scirp.94010-ref75">75</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref76">76</xref>] . Saponins reduce protein digestibility by the formation of sparingly digestible saponin-protein complexes [<xref ref-type="bibr" rid="scirp.94010-ref77">77</xref>] . Endogenous saponins affects the chymotrypsic hydrolysis of soyabean protein, particularly glycinin [<xref ref-type="bibr" rid="scirp.94010-ref78">78</xref>] . Saponins have been reported to be highly toxic to fish because of their damaging effect on the respiratory epithelia [<xref ref-type="bibr" rid="scirp.94010-ref79">79</xref>] . They are also considered to be the active components of many traditionally used fish poisons, like mahua oil cake [<xref ref-type="bibr" rid="scirp.94010-ref80">80</xref>] . Quin and Xu found that the butanol extract of Mussaenda pubescens was capable of terminating pregnancy in rats [<xref ref-type="bibr" rid="scirp.94010-ref81">81</xref>] . Saponins exhibit abortifacient, anti-zygotic and anti-implantation properties and are often used as contraceptives in many places [<xref ref-type="bibr" rid="scirp.94010-ref73">73</xref>] . Saponin isolates have also shown specific inhibition on the growth of cancer cell in vitro [<xref ref-type="bibr" rid="scirp.94010-ref82">82</xref>] , and anti-oxidant properties [<xref ref-type="bibr" rid="scirp.94010-ref83">83</xref>] .</p><p>&#183; Alkaloids: Alkaloids are a group of complex nitrogen containing compounds derived from microbes, marine organisms and plants. Alkaloids are structurally diverse with over 12,000 structures elucidated from plants [<xref ref-type="bibr" rid="scirp.94010-ref84">84</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref85">85</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref86">86</xref>] . Well known alkaloid compounds include-purine alkaloids (caffeine, theobromine), tropane alkaloids (cocaine, scopolamine), benzyl isoquinoline alkaloids (berberine, morphine) and monoterpenol indole alkaloids (vinblastine, ajmaline). Alkaloids are classified based on their primary metabolite purine alkaloids that are produced from adenine or guanine. Tropane alkaloids (TA) are produced from ornithine, Isoquinoline alakloids (IQA) are produced from tyrosine, Monoterpenoid indole alkaloids (MIA) derived from tryptophan [<xref ref-type="bibr" rid="scirp.94010-ref87">87</xref>] . They are used widely as anti-cancer agents, anti-malarials and analgesic and in the treatment of Parkinson’s hypertension and central nervous system disorders [<xref ref-type="bibr" rid="scirp.94010-ref88">88</xref>] .</p><p>&#183; Tannins: Tannins (tannic acids) are naturally occurring complex chemicals found in plants. They are of two distinct types: Hydrolysable tannins (polyesters of gallic acid) and Condensed tannins [<xref ref-type="bibr" rid="scirp.94010-ref89">89</xref>] . Hydrolysable tannins are gallic acid and egallic acid that consist of polyols such as sugars and phenolics such as Catechin. P-Penta-O-galloyl-D-glucose is tannic acid and is the model compound for this group of tannins. Hydrolysable tannins are further classified according to the products of hydrolysis; gallotannins yield gallic acid and glucose, and ellagitannins yield ellagic acid and glucose [<xref ref-type="bibr" rid="scirp.94010-ref90">90</xref>] . Condensed tannins include Pro-anthocyanidins that are polymers of flavan 3-ols linked through an interflavan carbon bond. Thus more accurate definitions are needed and the most unambiguous tannin definition is based on their chemical structures. In addition to their fundamental activities, i.e., binding to proteins, large molecular compounds and metallic ions, and also exhibiting antioxidant activities. Some structure-specific activities were found for the condensation of dehydroellagitannins with co-existing compounds under mild conditions, and the host-mediated antitumor actions of ellagitannin oligomers [<xref ref-type="bibr" rid="scirp.94010-ref91">91</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref92">92</xref>] .</p><p>&#183; Cardiac glycosides: The aglycone part of cardiac glycosides is a tetracyclic steroid with an attached unsaturated lactone ring that may have 5 or 6 members. Cardiac glycosides are classified into two groups according to the lactone ring: the C-23 cardenolides with an α,β-unsaturated δ-γ-lactone (butenolide) and the C-24 bufadienolides with a di-unsaturated γ-lactone (pentadienolide). Majority of saccharides found in cardiac glycosides are highly specific. They are 2,6dideoxyhexoses, such as D-digitoxose, L-oleandrose or D-diginose. Cardiac glycosides such as digitoxin from Digitalis have been used as drugs for the treatment of cardiac insufficiency. Apart from that cardiac glycosides are also being used in the treatment of cancer. These compounds typically inhibit cancer cell proliferation and growth and activate tumor-specific immune responses. They are ligands for Na/K-ATPase, which is a promising drug target in cancer [<xref ref-type="bibr" rid="scirp.94010-ref93">93</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref94">94</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref95">95</xref>] .</p></sec><sec id="s1_7"><title>1.7. Traditional Medicine and Anti-Cancer Properties</title><p>Cancer is a major global health burden with approx 10.9 million new cases, 6.7 million deaths and 24.6 million surviving patients all around the world since 2002 [<xref ref-type="bibr" rid="scirp.94010-ref96">96</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref97">97</xref>] . Since 1990, there has been 22% increase in cancer cases and mortality, with most frequent cancers being lung, breast, colorectal, stomach, oral, skin and ovary [<xref ref-type="bibr" rid="scirp.94010-ref98">98</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref99">99</xref>] .</p><p>Thus it has become necessary to investigate new strategies to prevent and treat cancer. Medicinal plant derivatives and secondary metabolites have played important roles in the treatment of cancer. The National Cancer Institute has collected about 35,000 plant samples from 20 countries and screened out 114,000 extracts for anti-cancer activity [<xref ref-type="bibr" rid="scirp.94010-ref97">97</xref>] . Of all the available anti-cancer drugs during 1940-2002, 40% were natural products or their derivatives, another 8% were natural products mimics [<xref ref-type="bibr" rid="scirp.94010-ref100">100</xref>] . Anti-cancer agents from medicinal plants that are currently in use can be grouped into four classes of compounds: Vinca (or Catharanthus) alkaloids, epipodophyllotoxins, taxanes and camptothecins. Vinblastine and vincristine are isolated from Catharanthus roseus and have been clinically used for over 40 years [<xref ref-type="bibr" rid="scirp.94010-ref101">101</xref>] , for a variety of cancers including leukemia, lymphomas, advanced testicular cancer, breast and lung cancers and Kaposi’s sarcoma [<xref ref-type="bibr" rid="scirp.94010-ref100">100</xref>] . The mechanism of action of vinca alkaloids and several other semi-synthetic derivatives is blocking mitosis with metaphase arrest, which occurs by binding specifically to tubulin resulting in its depolymerization [<xref ref-type="bibr" rid="scirp.94010-ref102">102</xref>] . Podophyllotoxin isolated from resin of Podophyllum peltatum was found to be too toxic to host so its derivatives were made [<xref ref-type="bibr" rid="scirp.94010-ref103">103</xref>] . Etoposide and teniposide are two semi-synthetic derivatives of epipodophyllotoxin and are used in the treatment of lymphomas, bronchial and testicular cancers [<xref ref-type="bibr" rid="scirp.94010-ref100">100</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref102">102</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref103">103</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref104">104</xref>] . The epipodophyllotoxin binds tubulin, causing DNA strand breaks during the G2 phase of the cell cycle by irreversibly inhibiting DNA topoisomerase II [<xref ref-type="bibr" rid="scirp.94010-ref103">103</xref>] . Paclitaxel was isolated from Taxus brevifolia and is significantly active against ovarian cancer, advanced breast cancer, small and non-small cell lung cancer [<xref ref-type="bibr" rid="scirp.94010-ref105">105</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref106">106</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref107">107</xref>] . The taxanes including Paclitaxel and its derivatives act by binding to tubulin without allowing depolymerization or interfering with tubulin assembly [<xref ref-type="bibr" rid="scirp.94010-ref108">108</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref109">109</xref>] . The cells show defects in mitotic spindle assembly, chromosome segregation, and cell division and are unable to achieve metaphase spindle configuration. The spindle inhibition role is attributed to suppress the microtubules dynamics and occurs at lower concentrations than those needed to block mitosis. Camptothecin isolated from Camptotheca acuminata, originally showed unacceptable myelosuppression [<xref ref-type="bibr" rid="scirp.94010-ref105">105</xref>] - [<xref ref-type="bibr" rid="scirp.94010-ref112">112</xref>] . However, interest in Camptothecin revived when it was found to be selective inhibitor of topoisomerase I, involved in cleavage and reassembly of DNA [<xref ref-type="bibr" rid="scirp.94010-ref112">112</xref>] . The effect causes damage in DNA and apoptosis of the cancer cells due to the conversion of single-strand break into double-strand break resulting from the collision of the replication fork at cleavable complex. Together taxanes and camptothecins account for approximately one third of the global anti-cancer market in 2002. Numerous derivatives of all four compound classes are currently in clinical use. There are more than 270,000 plants existing on this planet waiting to be explored [<xref ref-type="bibr" rid="scirp.94010-ref113">113</xref>] . Here we have also mentioned some of plant active principles and there activity on different cancer cell lines with structural formulas in <xref ref-type="table" rid="table1">Table 1</xref>.</p></sec><sec id="s1_8"><title>1.8. TM/CAM Safety Features</title><p>Secondary metabolites are in great demand due to their inexpensiveness, better cultural acceptability, and better compatibility with minimal side effects [<xref ref-type="bibr" rid="scirp.94010-ref159">159</xref>] . They are relatively safe because they are derived from natural compounds rendering less toxicity [<xref ref-type="bibr" rid="scirp.94010-ref160">160</xref>] . They are also potential source of chemical constituents with anti-tumor and cytotoxic activities [<xref ref-type="bibr" rid="scirp.94010-ref161">161</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref162">162</xref>] . They have anti-cancerous potential due to occurrence of natural antioxidants acting as reducing agents, free radical scavengers and quenchers of singlet oxygen. Greater part of their antioxidant action is due to bioactive compounds viz flavones, isoflavones, flavonoids, anthocyanins, coumarins, lignans, catechins and isocatechins that help in reducing or minimizing the toxic side effect of conventional treatments [<xref ref-type="bibr" rid="scirp.94010-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref163">163</xref>] .</p></sec></sec><sec id="s2"><title>2. Limitations</title><p>The traditional medicine takes long time to act and gives response towards the disease in slow manner. The active principles of medicinal plants are also allergic sometimes. Herbal medicines are not effective in case of cancer, chronic diseases, and sudden illness and auto immune diseases. Herbal medicines isolation and characterization for the drug discovery have numerous limitations, if incorrect identification is done it can lead to serious side effects. It is generally observed that herbal medicines are not properly regulated because it has so many secondary metabolites such that it does not show quality assurance. While using active plant derived secondary metabolites having obstacles toward the cancer and other chronic diseases: Plant active secondary metabolites may vary regions to region according to geographical with lack of definite safety consideration behalf of specificity and sensitivity because its highly complex active personalized ingredient for specific formulations in addition one of the major drawbacks of the plant metabolite is lack of defined molecular targets.</p></sec><sec id="s3"><title>3. Future Prospects and Applications</title><p>In the future, each patient should have their own unique chemotherapy protocol, which improves the therapeutic quality by selecting and prescribing</p><table-wrap-group id="1"><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> In vitro effects of various bioactive compounds: mechanism, structure on various cancer cell line</title></caption><table-wrap id="1_1"><table><tbody><thead><tr><th align="center" valign="middle" >Cancer type</th><th align="center" valign="middle"  colspan="2"  >Active Compound and Structural Formula</th><th align="center" valign="middle" >Mechanism of action</th><th align="center" valign="middle" >Cell lines</th><th align="center" valign="middle" >References</th></tr></thead><tr><td align="center" valign="middle"  rowspan="15"  >Breast cancer</td><td align="center" valign="middle"  rowspan="5"  >FLAVONOIDS</td><td align="center" valign="middle" >Flavanones (C<sub>15</sub>H<sub>10</sub>O<sub>3</sub>)</td><td align="center" valign="middle"  rowspan="5"  >Inhibition of the Epidermal Growth Factor (EGF) receptor in the sub-micromolar range by competing with ATP for its binding site.</td><td align="center" valign="middle"  rowspan="5"  >MCF-7</td><td align="center" valign="middle"  rowspan="5"  >[<xref ref-type="bibr" rid="scirp.94010-ref114">114</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref115">115</xref>]</td></tr><tr><td align="center" valign="middle" >Daidzein (C<sub>15</sub>H<sub>10</sub>O<sub>4</sub>)</td></tr><tr><td align="center" valign="middle" >Genistein (C<sub>15</sub>H<sub>10</sub>O<sub>5</sub>)</td></tr><tr><td align="center" valign="middle" >Quercetin (C<sub>15</sub>H<sub>10</sub>O<sub>7</sub>)</td></tr><tr><td align="center" valign="middle" >Luteolin (C<sub>15</sub>H<sub>10</sub>O<sub>6</sub>)</td></tr><tr><td align="center" valign="middle"  rowspan="4"  >ALKALOIDS</td><td align="center" valign="middle" >Vinblastin (C<sub>46</sub>H<sub>58</sub>N<sub>4</sub>O<sub>9</sub>)</td><td align="center" valign="middle"  rowspan="4"  >Cellular microtubules stabilization by binding to β-tubulin subunit, causing interference in their normal breakdown during cell division, with resultant stabilization of the polymer through protection from disassembly.</td><td align="center" valign="middle"  rowspan="4"  >MDA-MB-231 MCF-7</td><td align="center" valign="middle"  rowspan="4"  >[<xref ref-type="bibr" rid="scirp.94010-ref116">116</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref117">117</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref118">118</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref119">119</xref>]</td></tr><tr><td align="center" valign="middle" >Vincristine (C<sub>46</sub>H<sub>56</sub>N<sub>4</sub>O<sub>10</sub>)</td></tr><tr><td align="center" valign="middle" >Taxol (C<sub>47</sub>H<sub>51</sub>NO<sub>14</sub>)</td></tr><tr><td align="center" valign="middle" >Noscapine (C<sub>22</sub>H<sub>23</sub>NO<sub>7</sub>)</td></tr><tr><td align="center" valign="middle" >SAPONINS</td><td align="center" valign="middle" >Saponins (C<sub>44</sub>H<sub>70</sub>O<sub>17</sub>)</td><td align="center" valign="middle" >Induce cell cycle (G1) arrest, Apoptotic and anti-proliferative activity.</td><td align="center" valign="middle" >MDA-MB-453, MCF-7</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.94010-ref120">120</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref121">121</xref>]</td></tr><tr><td align="center" valign="middle" >TANNINS</td><td align="center" valign="middle" >Maplexins A (C<sub>13</sub>H<sub>16</sub>O<sub>9</sub>)</td><td align="center" valign="middle" >Inhibition of cellular proliferation.</td><td align="center" valign="middle" >MCF-7, MCF7/HER2, JIMT-1</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.94010-ref122">122</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref123">123</xref>]</td></tr><tr><td align="center" valign="middle"  rowspan="4"  >CARDIAC GLYCOSIDES</td><td align="center" valign="middle" >Digitoxin (C<sub>41</sub>H<sub>64</sub>O<sub>13</sub>)</td><td align="center" valign="middle"  rowspan="4"  >Inhibition of Topoisomerases I and II.</td><td align="center" valign="middle"  rowspan="4"  >MCF-7, MDA-MD-435</td><td align="center" valign="middle"  rowspan="4"  >[<xref ref-type="bibr" rid="scirp.94010-ref124">124</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref125">125</xref>]</td></tr><tr><td align="center" valign="middle" >Digoxin (C<sub>41</sub>H<sub>64</sub>O<sub>14</sub>)</td></tr><tr><td align="center" valign="middle" >Proscillaridin (C<sub>30</sub>H<sub>42</sub>O<sub>8</sub>)</td></tr><tr><td align="center" valign="middle" >Ouabain (C<sub>29</sub>H<sub>44</sub>O<sub>12</sub>)</td></tr><tr><td align="center" valign="middle"  rowspan="6"  >Leukemia</td><td align="center" valign="middle"  rowspan="6"  >FLAVONOIDS</td><td align="center" valign="middle" >Sophoranone (C<sub>30</sub>H<sub>36</sub>O<sub>4</sub>)</td><td align="center" valign="middle"  rowspan="6"  >Inhibition of cell growth Induction of apoptosis. Induction of phase II metabolizing enzymes such as glutathione-S-transferase, quinine reductase, and UDP-glucuronyltransferase resulting in detoxification and elimination of carcinogens from the body.</td><td align="center" valign="middle"  rowspan="6"  >U937 cells,HL-60, K562, Jurkat</td><td align="center" valign="middle"  rowspan="6"  >[<xref ref-type="bibr" rid="scirp.94010-ref126">126</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref127">127</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref128">128</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref129">129</xref>]</td></tr><tr><td align="center" valign="middle" >Genistein (C<sub>15</sub>H<sub>10</sub>O<sub>5</sub>)</td></tr><tr><td align="center" valign="middle" >Apigenin (C<sub>15</sub>H<sub>10</sub>O<sub>5</sub>)</td></tr><tr><td align="center" valign="middle" >Quercetin (C<sub>15</sub>H<sub>10</sub>O<sub>7</sub>)</td></tr><tr><td align="center" valign="middle" >Myricetin (C<sub>15</sub>H<sub>10</sub>O<sub>8</sub>)</td></tr><tr><td align="center" valign="middle" >Chalcones (C<sub>15</sub>H<sub>12</sub>O)</td></tr></tbody></table></table-wrap><table-wrap id="1_2"><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="9"  ></th><th align="center" valign="middle"  rowspan="3"  >ALKALOIDS</th><th align="center" valign="middle" >Vinblastin (C<sub>46</sub>H<sub>58</sub>N<sub>4</sub>O<sub>9</sub>)</th><th align="center" valign="middle"  rowspan="3"  >Inhibition of cellular proliferation by altering the dynamics of tubulin addition and loss at the ends of mitotic spindle microtubules.</th><th align="center" valign="middle"  rowspan="3"  >CCRF-CEM CEM/VM-1</th><th align="center" valign="middle"  rowspan="3"  >[<xref ref-type="bibr" rid="scirp.94010-ref119">119</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref130">130</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref131">131</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref132">132</xref>]</th></tr></thead><tr><td align="center" valign="middle" >Vincristine (C<sub>46</sub>H<sub>56</sub>N<sub>4</sub>O<sub>10</sub>)</td></tr><tr><td align="center" valign="middle" >Cryptolepine (C<sub>16</sub>H<sub>12</sub>N<sub>2</sub>)</td></tr><tr><td align="center" valign="middle" >SAPONINS</td><td align="center" valign="middle" >Saponin (C<sub>44</sub>H<sub>70</sub>O<sub>17</sub>)</td><td align="center" valign="middle" >Causes cytotoxicity and apoptosis in tumor cells.</td><td align="center" valign="middle" >Jurkat, HL 60</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.94010-ref120">120</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref133">133</xref>]</td></tr><tr><td align="center" valign="middle"  rowspan="5"  >CARDIAC GLYCOSIDES</td><td align="center" valign="middle" >Bufalin (C<sub>24</sub>H<sub>34</sub>O<sub>4</sub>)</td><td align="center" valign="middle"  rowspan="5"  >Inhibition of topoisomerases I and II, Increased activation of MAPKs, Down regulation of cyclin A, Bcl-2 and BclxL, Increased expression of p21 and Bax.</td><td align="center" valign="middle"  rowspan="5"  >HL60, U-937, CCRF-CEM, CEM-VM-1</td><td align="center" valign="middle"  rowspan="5"  >[<xref ref-type="bibr" rid="scirp.94010-ref125">125</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref134">134</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref135">135</xref>]</td></tr><tr><td align="center" valign="middle" >Oleandrin (C<sub>32</sub>H<sub>48</sub>O<sub>9</sub>)</td></tr><tr><td align="center" valign="middle" >Digitoxin (C<sub>41</sub>H<sub>64</sub>O<sub>13</sub>)</td></tr><tr><td align="center" valign="middle" >Proscillaridin A (C<sub>30</sub>H<sub>42</sub>O<sub>8</sub>)</td></tr><tr><td align="center" valign="middle" >Ouabain (C<sub>29</sub>H<sub>44</sub>O<sub>12</sub>)</td></tr><tr><td align="center" valign="middle"  rowspan="2"  >Stomach</td><td align="center" valign="middle" >FLAVONOIDS</td><td align="center" valign="middle" >Sophoranone (C<sub>30</sub>H<sub>36</sub>O<sub>4</sub>)</td><td align="center" valign="middle" >Inhibition of cellular growth and induction of apoptosis. Inhibition, reversion or retardation of cellular hyperproliferation.</td><td align="center" valign="middle" >MKN7 cells</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.94010-ref136">136</xref>]</td></tr><tr><td align="center" valign="middle" >SAPONINS</td><td align="center" valign="middle" >Saponins (C<sub>44</sub>H<sub>70</sub>O<sub>17</sub>)</td><td align="center" valign="middle" >Cytotoxic effects on tumor cells.</td><td align="center" valign="middle" >SGC-7901</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.94010-ref137">137</xref>]</td></tr><tr><td align="center" valign="middle"  rowspan="9"  >Colon Cancer</td><td align="center" valign="middle"  rowspan="4"  >FLAVONOIDS</td><td align="center" valign="middle" >Flavone (C<sub>15</sub>H<sub>10</sub>O<sub>2</sub>)</td><td align="center" valign="middle"  rowspan="4"  >Inhibition of cellular proliferation and cytotoxicity, Perturbations in cell cycle progression. Checkpoints at both G1/S and G2/M of the cell cycle.</td><td align="center" valign="middle"  rowspan="4"  >Caco-2 and HT-29</td><td align="center" valign="middle"  rowspan="4"  >[<xref ref-type="bibr" rid="scirp.94010-ref138">138</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref139">139</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref140">140</xref>]</td></tr><tr><td align="center" valign="middle" >Quercetin (C<sub>15</sub>H<sub>10</sub>O<sub>7</sub>)</td></tr><tr><td align="center" valign="middle" >Genistein (C<sub>15</sub>H<sub>10</sub>O<sub>5</sub>)</td></tr><tr><td align="center" valign="middle" >Anthocyanin (C<sub>15</sub>H<sub>11</sub>O+)</td></tr><tr><td align="center" valign="middle"  rowspan="4"  >ALKALOIDS</td><td align="center" valign="middle" >Camptothecin (C<sub>20</sub>H<sub>16</sub>N<sub>2</sub>O<sub>4</sub>)</td><td align="center" valign="middle"  rowspan="4"  >It involves binding topoisomerase I–DNA covalent complex, forming a ternary complex that gets stabilized and DNA is prevented from religation during replication, that leads to damage in DNA and apoptosis of the cancer cells as single-strand break converts into double-strand break</td><td align="center" valign="middle"  rowspan="4"  >CaCo2, T84</td><td align="center" valign="middle"  rowspan="4"  >[<xref ref-type="bibr" rid="scirp.94010-ref141">141</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref142">142</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref143">143</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref144">144</xref>]</td></tr><tr><td align="center" valign="middle" >Topotecan (C<sub>23</sub>H<sub>23</sub>N<sub>3</sub>O<sub>5</sub>)</td></tr><tr><td align="center" valign="middle" >Irinotecan (C<sub>33</sub>H<sub>38</sub>N<sub>4</sub>O<sub>6</sub>)</td></tr><tr><td align="center" valign="middle" >Arctigenin (C<sub>21</sub>H<sub>24</sub>O<sub>6</sub>)</td></tr><tr><td align="center" valign="middle" >SAPONINS</td><td align="center" valign="middle" >Saponins (C<sub>44</sub>H<sub>70</sub>O<sub>17</sub>)</td><td align="center" valign="middle" >Inhibits cell proliferation through accumulation in S phase and G2/M arrest, with concomitant suppression of p21 expression and inhibition of cyclin-dependent kinase activity.</td><td align="center" valign="middle" >HT-29, C26</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.94010-ref145">145</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref146">146</xref>]</td></tr></tbody></table></table-wrap><table-wrap id="1_3"><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >TANNINS</th><th align="center" valign="middle" >Maplexins A –I (C<sub>13</sub>H<sub>16</sub>O<sub>9</sub>)</th><th align="center" valign="middle" >Down-regulation of cyclins A and B1 and upregulating of cyclin E, cell-cycle arrest in S phase, induction of apoptosis via intrinsic pathway (FAS-independent, caspase 8-independent) through bcl-XL down-regulation with mitochondrial release of cytochrome c into the cytosol, activation of initiator caspase 9 and effector caspase-3.</th><th align="center" valign="middle" >HCT-116, Caco-2, CCD-112CoN</th><th align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.94010-ref147">147</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref148">148</xref>]</th></tr></thead><tr><td align="center" valign="middle"  rowspan="10"  >Oral Cancer</td><td align="center" valign="middle"  rowspan="9"  >FLAVONOIDS</td><td align="center" valign="middle" >Flavanones (C<sub>15</sub>H<sub>10</sub>O<sub>3</sub>)</td><td align="center" valign="middle"  rowspan="9"  >Interaction with phase I metabolizing enzymes (e.g., cytochrome P450), which metabolically inactivate a large number of procarcinogens.</td><td align="center" valign="middle"  rowspan="9"  >HSC-2, HSG, SCC-25</td><td align="center" valign="middle"  rowspan="9"  >[<xref ref-type="bibr" rid="scirp.94010-ref149">149</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref150">150</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref151">151</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref152">152</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref153">153</xref>]</td></tr><tr><td align="center" valign="middle" >Isoflavonone (C<sub>15</sub>H<sub>12</sub>O<sub>2</sub>)</td></tr><tr><td align="center" valign="middle" >EGC (C<sub>15</sub>H<sub>14</sub>O<sub>7</sub>)</td></tr><tr><td align="center" valign="middle" >Chalcones (C<sub>15</sub>H<sub>12</sub>O)</td></tr><tr><td align="center" valign="middle" >EGCG (C<sub>22</sub>H<sub>18</sub>O<sub>11</sub>)</td></tr><tr><td align="center" valign="middle" >Curcumin (C<sub>21</sub>H<sub>20</sub>O<sub>6</sub>)</td></tr><tr><td align="center" valign="middle" >Genistein (C<sub>15</sub>H<sub>10</sub>O<sub>5</sub>)</td></tr><tr><td align="center" valign="middle" >Quercetin, (C<sub>15</sub>H<sub>10</sub>O<sub>7</sub>)</td></tr><tr><td align="center" valign="middle" >Cisplatin (C<sub>20</sub>H<sub>28</sub>N<sub>12</sub>O<sub>9</sub>PPt+)</td></tr><tr><td align="center" valign="middle" >TANNINS</td><td align="center" valign="middle" >Total Pomegranate Tannin (TPT) extract</td><td align="center" valign="middle" >Anti-proliferative activity</td><td align="center" valign="middle" >KB, CAL27</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.94010-ref147">147</xref>]</td></tr><tr><td align="center" valign="middle"  rowspan="6"  >Lung Cancer</td><td align="center" valign="middle"  rowspan="2"  >FLAVONOID</td><td align="center" valign="middle" >Flavone (C<sub>15</sub>H<sub>10</sub>O<sub>2</sub>)</td><td align="center" valign="middle"  rowspan="2"  >Inhibition of tyrosine kinases.</td><td align="center" valign="middle"  rowspan="2"  >SK-LU1, SW900, H441, H661, haGo-K-1, A549</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.94010-ref154">154</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref155">155</xref>]</td></tr><tr><td align="center" valign="middle" >Quercetin (C<sub>15</sub>H<sub>10</sub>O<sub>7</sub>)</td></tr><tr><td align="center" valign="middle"  rowspan="4"  >ALKALOID</td><td align="center" valign="middle" >Vinblastin (C<sub>46</sub>H<sub>58</sub>N<sub>4</sub>O<sub>9</sub>)</td><td align="center" valign="middle"  rowspan="4"  >Inhibition of cellular proliferation by altering the dynamics of tubulin addition and loss at the ends of mitotic spindle microtubules.</td><td align="center" valign="middle"  rowspan="4"  >A549</td><td align="center" valign="middle"  rowspan="4"  >[<xref ref-type="bibr" rid="scirp.94010-ref117">117</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref119">119</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref141">141</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref156">156</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref157">157</xref>]</td></tr><tr><td align="center" valign="middle" >Vincristine (C<sub>46</sub>H<sub>56</sub>N<sub>4</sub>O<sub>10</sub>)</td></tr><tr><td align="center" valign="middle" >Taxol (C<sub>47</sub>H<sub>51</sub>NO<sub>14</sub>)</td></tr><tr><td align="center" valign="middle" >Camptothecin (C<sub>20</sub>H<sub>16</sub>N<sub>2</sub>O<sub>4</sub>)</td></tr></tbody></table></table-wrap><table-wrap id="1_4"><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  ></th><th align="center" valign="middle"  rowspan="2"  ></th><th align="center" valign="middle" >Sanguinarine (C<sub>20</sub>H<sub>14</sub>NO<sub>4</sub>)</th><th align="center" valign="middle"  rowspan="2"  ></th><th align="center" valign="middle"  rowspan="2"  ></th><th align="center" valign="middle"  rowspan="2"  ></th></tr></thead><tr><td align="center" valign="middle" >Chelerythrine (C<sub>21</sub>H<sub>18</sub>NO<sub>4</sub>)</td></tr><tr><td align="center" valign="middle"  rowspan="7"  ></td><td align="center" valign="middle"  rowspan="2"  ></td><td align="center" valign="middle" >Chelidonine (C<sub>20</sub>H<sub>19</sub>NO<sub>5</sub>)</td><td align="center" valign="middle"  rowspan="2"  ></td><td align="center" valign="middle"  rowspan="2"  ></td><td align="center" valign="middle"  rowspan="2"  ></td></tr><tr><td align="center" valign="middle" >Noscapine (C<sub>22</sub>H<sub>23</sub>NO<sub>7</sub>)</td></tr><tr><td align="center" valign="middle" >SAPONINS</td><td align="center" valign="middle" >Saponins (C<sub>44</sub>H<sub>70</sub>O<sub>17</sub>)</td><td align="center" valign="middle" >Apoptosis, cytotoxic activity.</td><td align="center" valign="middle" >A549, NCI-H727</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.94010-ref133">133</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref137">137</xref>]</td></tr><tr><td align="center" valign="middle"  rowspan="4"  >CARDIAC GLYCOSIDES</td><td align="center" valign="middle" >Digitoxin (C<sub>41</sub>H<sub>64</sub>O<sub>13</sub>)</td><td align="center" valign="middle"  rowspan="4"  >Initiates Apo2L/TRAIL apoptosis via increased expression of death receptors 4 and 5</td><td align="center" valign="middle"  rowspan="4"  >NCI-H-358, Calu1, Sklu1, NCI-H6, H69AR</td><td align="center" valign="middle"  rowspan="4"  >[<xref ref-type="bibr" rid="scirp.94010-ref158">158</xref>]</td></tr><tr><td align="center" valign="middle" >Digoxin (C<sub>41</sub>H<sub>64</sub>O<sub>14</sub>)</td></tr><tr><td align="center" valign="middle" >Ouabain (C<sub>29</sub>H<sub>44</sub>O<sub>12</sub>)</td></tr><tr><td align="center" valign="middle" >Oleandrin (C<sub>22</sub>H<sub>23</sub>NO<sub>7</sub>)</td></tr></tbody></table></table-wrap></table-wrap-group><p>well-matched drugs and avoiding ineffective ones [<xref ref-type="bibr" rid="scirp.94010-ref58">58</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref164">164</xref>] . Applying such individualized chemotherapeutics through a personalized chemotherapy regime will further improve the final outcome [<xref ref-type="bibr" rid="scirp.94010-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref165">165</xref>] . This will be accompanied by the identification and testing of novel, more specific and selective drugs either via synthetic routes or by purifying from herbal sources [<xref ref-type="bibr" rid="scirp.94010-ref166">166</xref>] . Although the novel chemotherapeutic agents will be more and more effective against the tumor cells, their toxicity to normal tissues as well as drug resistance remains the major obstacle for clinical use [<xref ref-type="bibr" rid="scirp.94010-ref167">167</xref>] . Personalized approach using various phytochemical compounds provides a new dimension to the standard cancer therapy for improving its outcome in a complex and complementary way [<xref ref-type="bibr" rid="scirp.94010-ref168">168</xref>] (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p>Medicinal plants are also important for pharmacological research and drug development, not only when plant constituents are used directly as therapeutic agents, but also as starting materials for the synthesis of drugs or as models for pharmacologically active compounds [<xref ref-type="bibr" rid="scirp.94010-ref169">169</xref>] [<xref ref-type="bibr" rid="scirp.94010-ref170">170</xref>] . Major pharmaceutical companies are presently conducting extensive research on plant materials gathered from various habitats for their potential medicinal value [<xref ref-type="bibr" rid="scirp.94010-ref171">171</xref>] . Rather than using whole plant, scientists identify, isolate, extract and synthesize individual active compounds. Because modern pharmacology looks for one active ingredient and seeks to isolate it to the segregation of all the others, most of the research</p><p>focuses on identifying and isolating active ingredients rather than studying the medicinal properties of the whole plant [<xref ref-type="bibr" rid="scirp.94010-ref172">172</xref>] . Despite the remarkable progress in the organic synthetic chemistry, over 25% of prescribed medicines are derived directly or indirectly from plants which need to be further explored for better clinical intervention in therapeutics [<xref ref-type="bibr" rid="scirp.94010-ref166">166</xref>] .</p><p>Acknowledgements</p><p>The authors would like to express their deepest gratitude to Department of Biochemistry, AIIMS, Bhopal.</p><p>Conflicts of Interest</p><p>The authors declare that there are no conflicts of interest.</p><p>References</p></sec></body><back><ref-list><title>References</title><ref id="scirp.94010-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Nema, R., Khare, S., Jain, P., Pradhan, A., Gupta, A. and Singh, D. (2013) Natural Products Potential and Scope for Modern Cancer Research. 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