The aim of the present study was to determine the level of underlying DNA damage in females with PCOS. Twenty-two women with PCOS and twenty-two healthy controls were included in this study. Patients were further categorized into three phenotypic subgroups:
Subgroup A
, oligo/anovulation (ANOV) and polycystic ovaries (PCO);
Subgroup B
, hyperandrogenism (HA) as a main characteristic (HA + ANOV or HA + PCO);
Subgroup C
, all three conditions present (HA + ANOV + PCO). The frequency of sister chromatid exchanges (SCEs) was used as an index of cytogenetic damage. Pro
liferation rate index (PRI), mitotic index (MI), average generation time (AGT) and population
doubling time (PDT) were also evaluated. A significant (p < 0.01) increase in SCE levels along with a significant (p < 0.01) reduction in PRIs and MIs were observed in women with PCOS compared with healthy subjects. Additionally, subgroup C demonstrated statistically significant differences compared with others, while subgroup A had similar results with healthy females. Our results suggest that females with PCOS show increased chromosomal instability in peripheral lymphocytes and a consequent inability of the cells to promote their own mitotic cycle. A positive correlation between DNA damage and PCOS phenotypes is also reported.
Polycystic Ovary Syndrome Proliferative Rate Index Mitotic Index Genotoxicity Cytostaticity1. Introduction
Polycystic ovary syndrome (PCOS) is one of the most common endocrine disorders amongst women of reproductive age. It is characterized by hyperandrogenism, menstrual disturbances, infertility due to chronic anovulation and polycystic ovaries [1] . Previous studies have demonstrated that the prevalence of the syndrome in different populations ranges from 2% - 20%, depending on which diagnostic criteria are used [2] - [4] .
It is generally admitted that PCOS is a multifactorialdisorder that results from a combination of multiple gene polymorphisms under the influence of environmental factors [5] - [7] . Cytogenetic studies have shown that women with PCOS have increased damage in their genetic material [8] - [10] . Additionally, a relation between PCOS and X chromosome aneuploidy, including XX/XO mosaics and high proportion of X chromosome abnormal segregation has been reported in a limited number of studies [8] - [11] .
Today, cytogenetics provides several biomarkers for chromosomal instability assessment, one of which is thesister chromatid exchange (SCE) frequency in cells. SCE is a natural process that implicates the exchange of homologous genetic segments as a mode of repair mechanism. The methodology of SCEs has been proved to be a very useful tool with predictive value, for detecting harmful effects on DNA, caused by various physical and chemical factors. Increased frequency of this index reflects the existence of genotoxicity in cells and the subsequent failure of repair mechanisms to recover the damaged site. Several studies have reported that SCE analysis is a very sensitive method, able to detect mutagens and/or carcinogens [12] and maybe more sensitive than other cytogenetic endpoints, such as micronuclei and chromosome aberrations [13] . Additionally, Proliferation Rate Index (PRI) and Mitotic Index (MI) are sensitive indices of cellular toxicity by antimutagenic and chemotherapeutic agents [14] [15] .
The aim of the present study was the quantitative and qualitative evaluation of DNA damage on peripheral lymphocytes of females with PCOS through the SCE assay and the determination of a possible association between chromosomal instability and different phenotypes of the syndrome. In order to reveal any underlying chromosome instability, irinotecan (CPT-11), a known antineoplasticdrug, was used as a positive control to produce SCEs. CPT-11 acts as an inhibitor of topoisomerase I, an essential enzyme in the DNA replication [16] , increasing chromosomal aberrations and reducing cell viability.
2. Materials and Methods2.1. Patients
Heparinized blood samples were received from 22 females (average age 26.4 years) newly diagnosed with PCOS and 22 healthy women (average age 29.5 years) served as control subjects. PCOS was diagnosed according to the Rotterdam consensus criteria [17] . The patients were further divided into three subgroups according to the phenotypic characteristics. Subgroup A includes 4 patients with ovulatory dysfunction: oligo- and/or anovulation (ANOV) and polycystic ovaries (PCO), Subgroup B includes 6 patients who are positive in two of three criteria including hyperandrogenism (HA) (HA + ANOV or HA + PCO), while Subgroup C contains 12 patients with all three conditions present (HA + ANOV + PCO). All samples were obtained from the Department of Obstetrics and Gynaecology of Alexandroupolis University Hospital. All participants were fully informed and gave written consent. The study protocol was approved by the University General Hospital of Alexandroupolis Ethics Committee.
2.2. Protocol
Cultures of peripheral lymphocytes were prepared in universal containers by adding 11 drops of whole blood to 5 ml of Chromosome Medium B (Biochrom KG, Berlin, Germany). At the beginning of the culture period, CPT-11 and 5-bromodeoxyuridine (BrdU) were added ata finalconcentration of 50 ng/ml and 5 μg/ml, respectively. The cultures were incubated at 37˚C for 72 h. After 70 h, 0.5 μg/ml of Colcemide was added for additional incubation of 2 h. Cell harvesting followed. The chromosomes were stained by a modified Fluorescence plus Giemsa (FPG) technique [14] .
Three main indices were evaluated: a) SCEs, which is a qualitative and quantitative index of genotoxicity, b) the mitotic index (MI), which is a qualitative index of cytotoxicity and c) the proliferation rate index (PRI), which is a qualitative index of cytostaticity. In relation to cell cycle kinetics the Average generation time (AGT) and the Population doubling time (PDT) were also estimated.
Mean SCE levels were evaluated only in suitable second division metaphases. 20 well spread and differentiated metaphases were counted per culture, because only at this stage were we able to observe and count them (Figure 1 and Figure 2). In order to establish PRI, 200 cells were counted and the following formula was used: PRI = (M1 + 2M2 + 3M3+)/N, where M1 is the percentage of cells at first division, M2 is the percentage of cells at second division and M3+ is the percentage of cells at third and subsequent divisions, while N is the total number of cells counted. For the MIs, 2000 activated lymphocytes were determined for each culture. The cell cycle time AGT was studied as the ratio of BrdU time and proliferation rate index, AGT = 72 h (BrdU time)/PRI. Finally, PDT is the time in which cells divide, i.e. in one cell cycle of 24 h. The following formula was used for this index: PDT = 24 h/PRI [18] .
A second-division metaphase after Fluorescence Plus Giemsa staining of a healthy woman blood lymphocyte, where all chromosomes have one lightly stained chromatid and one heavily stained chromatid (arrows show sister chromatid exchanges). Original magnification 1000×
A second-division metaphase after Fluorescence Plus Giemsa staining of a PCOS blood lymphocyte, where all chromosomes have one lightly stained chromatid and one heavily stained chromatid (arrows show sister chromatid exchanges). Original magnification 1000×
2.3. Statistical Analysis
One-way analysis of variance (ANOVA) was used to assess differences of SCE frequency between the two main groups and the subgroups of patients, while post hoc analysis was performed using Dunnett’s T3 test for pair-wise comparisons. Statistical evaluation of PRI, MI AGT and PDT was based on Chi-squared test. A probability p < 0.05 was considered as a statistically significance.
3. Results
Table 1 illustrates our findings in control group, PCOS group and PCOS subgroups. The cytogenetic parameters were remarkably different between the two main groups. Women with PCOS demonstrated a significantly (p < 0.01) increased SCE frequency at a percentage of 19.9%, having a mean value of 8.27 SCEs/cell compared with the control subjects having a mean value of 6.9 SCEs/cell in untreated cultures. The mutagenic agent CPT-11 gave rise to a significant increase in SCE levels in both groups. The values were estimated in 30.79 SCEs/cell and 35.05 SCEs/cell for controls and patients, respectively. Especially in PCOS patients, subgroup A had similar results with the control group. Subgroup B reveals statistically significant (p < 0.01) induction of SCE levels (8.28 SCEs/cell) in control lymphocyte cultures (without CPT-11 treatment) in comparison with subgroup A (6.99 SCEs/cell) and control group, but not with subgroup C (8.7 SCEs/cell). Subgroup C indicates the strongest chromosomal instability, which is obvious from the statistically significant (p < 0.01) induction of SCEs/cell with or without CPT administration.
As far as the mitotic index (MI) is concerned, patients showed significant (p < 0.01) reduction in the number of mitotic divisions (33.6‰) in comparison with healthy subjects (41.4‰). The cytotoxic activity of CPT-11 was exhibited in all cultures that were incubated. CPT-11 gave a significant decrease in the number of cell divisions at a percentage 16.96% in women with PCOS, but a greater reduction in healthy females at a percentage 18.84%. However, the MI values in CPT-11 cultures were 27.9‰ in patients and 33.6‰ in healthy subjects. Furthermore, subgroup C had lower values of MI than the other subgroups. Subgroup B showed a significant decrease in MI compared with subgroup A. Moreover, healthy women and subgroup A had similar results.
Finally, Table 1 exhibits details of the cell-cycle progression in the two main groups and PCOS subgroups. PCOS women illustrated a significant (p < 0.01) decrease in PRI and higher (p < 0.01) AGT and PDT values compared with control group (exposed or not to CPT agent). Additionally, subgroup C demonstrated higher cytostaticity, as revealed by the PRI, AGT and PDT values, followed by subgroup B and lastly by subgroup A.
4. Discussion
The SCE frequency in cultured lymphocytes has been used as biomarker of chromosomal damages for many years. In this paper we reported for the first time SCE frequencies in peripheral blood lymphocytes of women
Mean number of SCEs, mitotic index (MI) and proliferation rate index (PRI) in cultured peripheral lymphocytes of patients, healthy women and PCOS subgroups. Average generation time (AGT) and population doubling time (PDT) are also shown
Donors
Cultures
SCEs/cell ± SEM
Mitotic index (‰)
PRI
AGT
PDT
Control group
Control
6.90 ± 0.16
41.4
2.56
28.27
9.42
CPT-11
30.79 ± 0.53a
33.6a
2.46a
29.82a
9.94a
PCOS group
Control
8.27 ± 0.17b
33.6b
2.42b
29.93b
9.98b
CPT-11
35.05 ± 0.57ab
27.9ab
2.30ab
31.42ab
10.47ab
Subgroup A
Control
6.99 ± 0.35c
39.5c
2.55c
28.33c
9.44c
CPT-11
29.57 ± 1.01ad
34.4ac
2.44ac
29.27ac
9.76ac
Subgroup B
Control
8.28 ± 0.29e
36.2bc
2.46bc
29.50bc
9.83bc
CPT-11
30.78 ± 0.96ad
29.3abc
2.29af
31.62af
10.54af
Subgroup C
Control
8.70 ± 0.23e
30.3bc
2.27bc
31.85bc
10.62bc
CPT-11
39.01 ± 0.79bc
25.1abc
2.25f
32.46f
10.82f
ap < 0.01 vs control culture; bp < 0.01 vs control group; cp < 0.01vs other subgroups; dp < 0.01 vs subgroup C; ep < 0.01 vs control group and subgroup A; p < 0.05 vs control group and subgroup A.
with PCOS. Additionally, to the best of our knowledge this is the first study to investigate a possible association between chromosomal instability and clinical phenotypes of the syndrome. Our findings illustrated that the DNA of patients showed significant damage, as shown by the increased SCE frequency in lymphocytes, confirming some reports that deal with this issue [8] [19] . These reports suggest the presence of genetic abnormality in PCOS [9] [10] [20] . Whether the increased chromosomal instability in PCOS patients is a side effect of the disease process or is due to altered genetic background remains unclear. TheCPT-11 agentled to significant genotoxicity in both groups, but it elicited a higher increase in SCE levels in patients than in healthy individuals. The induction of SCEs depends on the agent activity, which is associated with a different mechanism of creation of SCEs and probably depends on the composition of genetic material [21] . Additionally, the high rate of DNA damage in PCOS patients suggests that the repair mechanisms are more “lenient” and/or insufficient to genetic changes. The malfunction and the consequently deficiency of DNA-repair mechanisms in PCOS women have been reported [22] .
Data from the control cultures of the two examined groups revealed the reduced viability and the inability of patients’ lymphocytes to promote their own mitotic cycle, which is demonstrated by the significant low PRI, MI, AGT and PDT values. The mutagenic agent CPT-11 had a higher cytostatic effect on patients than on healthy individuals. It is known that CPT-11 is involved in DNA replication and cell division, reducing cell viability [23] . However, it is worth pointing out that this factor caused a greater reduction ratio of MI in healthy women than in patients. A possible explanation for this observation could be the fact that healthy individuals whose genetic material had not undergone any crucial alterations were more responsive to cytotoxic agents.
Significant differences in cytogenetic indices emerged between the subgroups of patients. This study demonstrates a possible association of chromosomal instability and different PCOS phenotypes. More specifically, females with severe PCOS (3 of 3 criteria) had clearly higher genotoxicity, cytostaticity and cytotoxicity than the other phenotypes. Patients with ovulatory dysfunction (ANOV and PCO) demonstrated similar results with healthy individuals. This finding possibly reinforces the conviction of many scientists that this phenotype should not be taken into consideration as a PCOS case. Moreover, patients with HA and ovarian dysfunction (ANOV or PCO) demonstrated a significant increase in spontaneous SCE frequency and considerable reduction in the cell cycle progression, as exhibited by the decreased PRI and MI along with increased AGT and PDT in comparison with controls and subgroup A. The observation of increased chromosomal damage in phenotypes which have androgen excess as one of the main characteristics (B and C subgroups) reveals the potential role of HA in genetic instability. Indeed, positive correlation between free testosterone and DNA strand breakage has been reported in PCOS patients [24] . It is believed that testosterone and DHEAS may have pro-oxidant properties depending on their concentration [25] [26] . Therefore, these hormones may contribute to the induction of oxidative DNA damage in the form of strand breakage at high concentrations. Thus, it would not be too arbitrary to point out that the HA in PCOS is associated with chromosomal instability.
Genetic instability can have very serious consequences for PCOS patients. It has been proved that chromosomal abnormalities (structural, numerical) are associated with increased risk of cancer [27] and early miscarriages [28] . There are studies supporting the existence of these two phenomena in PCOS patients [29] [30] . It is generally accepted that PCOS is associated with gynaecological malignancies such as endometrial cancer and less with ovarian cancer. There is a weak relation between breast cancer and the syndrome [31] . It is worth pointing out that clinical investigators have shown that SCE levels are higher in patients with ovarian and breast cancer than healthy individuals [32] [33] . Therefore, the mutagenic process and the consequent cancer risk in these women probably can be clarified with SCEs.
5. Conclusion
In conclusion, in this study SCEs have been applied as a predictive assay of DNA damage risk and as a biomarker of mutagenicity. Spontaneous or baseline SCE frequencies in peripheral blood lymphocytes provide an additional diagnostic tool for identifying accumulated chromosomal damage occurring during the lifespan of the cells. Our results suggest that there is chromosomal instability in lymphocytes of PCOS patients, which is associated with phenotypic characteristics. Future studies should be conducted to confirm these findings.
Acknowledgements
We thank all the women for participating in this study.
Conflicts of Interest
The authors declare that there are no conflicts of interest. The authors alone are responsible for the content and writing of the paper.
Cite this paper
EvageliaDafa,MariaKontou,Tzegiaver B.Mantratzi,Emmanouel N.Kontomanolis,Nikoletta G.Koutlaki,Vasilios A.Liberis, Theodore S.Lialiaris, (2015) Enhancement of Sister Chromatid Exchanges (SCEs) in Peripheral Blood Lymphocytes of Women with Polycystic Ovary Syndrome (PCOS)in Vitro. Open Journal of Obstetrics and Gynecology, 05,378-384. doi: 10.4236/ojog.2015.57055
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