<?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">JCT</journal-id><journal-title-group><journal-title>Journal of Cancer Therapy</journal-title></journal-title-group><issn pub-type="epub">2151-1934</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jct.2013.48A004</article-id><article-id pub-id-type="publisher-id">JCT-36106</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Polymorphisms of GSTs in Lung Adenocarcinoma Patients Followed in the Context of a Biobank
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>otis</surname><given-names>Vlastos</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Georgios</surname><given-names>Hillas</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Nektarios</surname><given-names>Anagnostopoulos</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Jean</surname><given-names>Michel Vignaud</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Nadine</surname><given-names>Martinet</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Nikolaos</surname><given-names>G. Koulouris</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>Department of Respiratory Medicine, University of Athens Medical School, “Sotiria” Hospital, Athens, Greece</addr-line></aff><aff id="aff2"><addr-line>The Centre for Biological Resources of Nancy/U724 INSERM, Central Hospital, Cour d’Anatomie, Nancy, France</addr-line></aff><aff id="aff3"><addr-line>Laboratory of Chemistry of Bioactive Molecules, UMR CNRS 6001, Nice, France</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>aris.anag@yahoo.gr(OV)</email>;<email>aris.anag@yahoo.gr(GH)</email>;<email>aris.anag@yahoo.gr(NA)</email>;<email>aris.anag@yahoo.gr(JMV)</email>;<email>aris.anag@yahoo.gr(NM)</email>;<email>aris.anag@yahoo.gr(NGK)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>13</day><month>08</month><year>2013</year></pub-date><volume>04</volume><issue>08</issue><fpage>24</fpage><lpage>28</lpage><history><date date-type="received"><day>June</day>	<month>25th,</month>	<year>2013</year></date><date date-type="rev-recd"><day>July</day>	<month>28th,</month>	<year>2013</year>	</date><date date-type="accepted"><day>August</day>	<month>6th,</month>	<year>2013</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>
 
 
   <b>Background</b><b>: </b>Lung Adenocarcinoma (ADC) has been recently associated with distinct molecular changes, leading to the development of molecular-based targeted therapy. The Nancy’s Centre of Biological Resources (“Centre des Ressources Biologiques”, CRB) is an ISO 9001-2000 certified biobank with biological material and follow-up data from lung cancer patients, which collected during the last 20 years. <b>Objective</b><b>: </b>To estimate and compare the frequency of Glutathionne S-Transferase (GST) polymorphisms in a French population of ADC patients. <b>Methods</b><b>: </b>A retrospective study was conducted by the CRB between 1988 and 2007: 296 consecutive patients operated upon for ADC and 447 healthy subjects were evaluated. Genomic DNA was obtained from peripheral blood samples collected in EDTA tubes. The DNA was extracted using proteinase K digestion and phenol: chloroform purification. The GST polymorphisms were studied with duplex SYBR Green q PCR using specific primers and results being read on melt curves. <b>Results</b><b>: </b>Two GST classes were monitored during this research. The Mu class GST (GSTM) and the Theta class GST (GSTT) members. We studied the incidence of each genotype, as well as the GSTMT (combined Mu and Theta class) and null genotype in ADC and control patients. ADC patients had a higher incidence of the GSTM polymorphism (p &lt; 0.0001, 95%CI 1.63 - 3.24) and a lower incidence of the GSTT polymorphism (p &lt; 0.0001, 95%CI 0.31 - 0.66) comparing to control. The null and GSTMT genotype had no significant statistical differences between the two groups. <b>Conclusion</b><b>: </b>ADC patients were found to have a higher incidence of the GSTM genotype and a lower incidence of the GSTT genotype, compared to controls. Future studies may help elucidate the possible contribution of these genotypic differences in lung adenocarcinoma carcinogenesis or regarding the response to chemotherapy.
      
     
 
</p></abstract><kwd-group><kwd>GSTs; Molecular Signature; Lung Adenocarcinoma; Lung Cancer Risk</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Lung cancer was the first cause of cancer-related deaths in 2012 in the European Union with 353,000 deaths [<xref ref-type="bibr" rid="scirp.36106-ref1">1</xref>]. Tobacco smoking is the major attributable risk factor for the increasing prevalence of lung cancer across the world [<xref ref-type="bibr" rid="scirp.36106-ref2">2</xref>]. However, not all smokers are equally susceptible to tobacco-related carcinogens [<xref ref-type="bibr" rid="scirp.36106-ref3">3</xref>]. Thus, the identification of genes responsible for lung carcinogenesis susceptibility may allow researchers to perform screening programs and chemoprevention trials in subgroups of chronic smokers.</p><p>Lung Adenocarcinoma (ADC) has replaced squamous cell carcinoma as the most frequent histological subtype of lung cancer [4-7]. The Nancy’s Centre of Biological Resources (“Centre des Ressources Biologiques”, CRB) is an ISO 9001-2000 certified biobank with biological material and follow-up data from lung cancer patients, which collected during the last 20 years. Nancy’s CRB has been developed in the Nancy Central Hospital, aiming to recruit lung cancer patients willing to donate their samples for cancer research [<xref ref-type="bibr" rid="scirp.36106-ref8">8</xref>].</p><p>The French National Institute of Medical Research (INSERM) carried out this study aiming at the identification of biological tests associated with lung cancer risk. The tests included single nucleotide polymorphisms (SNP) of a family of detoxifying enzymes called Glutathione-S Transferases (GSTs). The activity of GSTs is dependent upon a steady supply of glutathione (GSH).</p><p>The primary role of GSTs is to detoxify xenobiotics by catalyzing the nucleophilic attack by GSH on xenobiotic substrates, thereby preventing their interaction with crucial cellular proteins and nucleic acids [9,10].</p><p>The aim of this study was to estimate and compare the frequency of GSTs polymorphisms in a French population of ADC patients. Therefore, we analysed genomic DNA from peripheral blood samples of lung adenocarcinoma patients and healthy controls.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Patients</title><p>A retrospective study was conducted by the CRB between 1988 and 2007: 743 subjects were evaluated (296 consecutive patients operated upon for ADC and 447 healthy subjects who were used as the control group).</p><p>The diagnosis of ADC was established by bronchial biopsies, cytological examination of sputum, bronchial washings and brushings and/or transthoracic fine needle aspiration of the lung lesion. All histological diagnoses had been confirmed by the same pathologists’ panel. The histological classification was based upon the 2004 World Health Organization guidelines [<xref ref-type="bibr" rid="scirp.36106-ref11">11</xref>]. The sixth edition of the TNM (tumor, node, and metastasis) classification was used [<xref ref-type="bibr" rid="scirp.36106-ref12">12</xref>].</p><p>The CRB collection was initiated in 1988 to store tissue samples of patients operated for lung tumors as a resource for research purposes. From 2002, all survivors—new patients and control subjects—were invited to give their written informed consent, offer access to their medical records, and to donate biological material for research. Standard operating procedures were followed for all steps of sample collection and storage and for the retrieval of clinical annotations culminating in ISO 9001 certification of the biobank.</p><p>All the procedures were carried out according to the principles of the institutional guidelines and the study was approved by the local Ethics Committee.</p></sec><sec id="s2_2"><title>2.2. Methods</title><p>Genomic DNA was obtained from peripheral blood samples (12 ml) collected in EDTA tubes. The DNA was extracted using proteinase K digestion and phenol: chloroform purification. The Mu class GST (GSTM) and the Theta class GST (GSTT) SNPs were studied with duplex SYBR Green q PCR using the primers described in <xref ref-type="table" rid="table1">Table 1</xref> and results being read on melt curves.</p></sec><sec id="s2_3"><title>2.3. Statistical Analysis</title><p>The Hardy-Weinberg equilibrium was tested with the χ<sup>2</sup> statistic for the goodness-to-fit (one degree of freedom). Statistical differences between groups were calculated by the χ<sup>2</sup> or Fischer’s exact test. Conditional analysis was used to obtain race, age and gender-adjusted crude odds ratios (OR). A p-value of &lt;0.05 was considered significant. All analyses were performed using the statistical package SPSS version 17.0.</p></sec></sec><sec id="s3"><title>3. Results</title><p><xref ref-type="table" rid="table2">Table 2</xref> summarizes the main epidemiological and clinical characteristics of the study population. ADC patients were found to present a higher incidence of GSTM (p &lt; 0.0001, 95%CI 1.63 - 3.24) and a lower incidence of GSTT (p &lt; 0.0001, 95%CI 0.31 - 0.66) genotypes comparing to control. The null and GSTMT genotype had no significant statistical differences between the two groups (<xref ref-type="table" rid="table3">Table 3</xref>).</p></sec></body><back><ref-list><title>References</title><ref id="scirp.36106-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">J. Ferlay, E. Steliarova-Foucher, J. Lortet-Tieulent, S. Rosso, J. W. Coebergh, H. Comber, D. Forman and F. Bray, “Cancer Incidence and Mortality patterns in Europe: Estimates for 40 Countries in 2012,” European Journal of Cancer, Vol. 49, No. 6, 2013, pp. 1374-1403.  
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