MassArray analysis of genomic susceptibility variants in ovarian cancer

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作者
Sonali Verma
Indu Sharma
Varun Sharma
Amrita Bhat
Ruchi Shah
Gh. Rasool Bhat
Bhanu Sharma
Divya Bakshi
Ashna Nagpal
Ajay Wakhloo
Audesh Bhat
Rakesh Kumar
机构
[1] Indian Council of Medical Research-Centre for Advance Research,Ancient DNA Laboratory
[2] Shri Mata Vaishno Devi University,School of Biotechnology
[3] Birbal Shani Institute of Paleo Sciences,Department of Biotechnology
[4] Shri Mata Vaishno Devi University,Department of Obstetrics and Gynecology
[5] Kashmir University,Centre for Molecular Biology
[6] Government Medical College,undefined
[7] Central University of Jammu,undefined
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Scientific Reports | / 10卷
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摘要
Ovarian cancer (OC), a multifaceted and genetically heterogeneous malignancy is one of the most common cancers among women. The aim of the study is to unravel the genetic factors associated with OC and the extent of genetic heterogeneity in the populations of Jammu and Kashmir (J&K).Using the high throughput Agena MassARRAY platform, present case control study was designed which comprises 200 histopathological confirmed OC patients and 400 age and ethnicity matched healthy controls to ascertain the association of previously reported eleven single nucleotide polymorphisms (SNPs) spread over ten genes (DNMT3A, PIK3CA, FGFR2, GSTP1, ERCC5, AKT1, CASC16, CYP19A1, BCL2 and ERCC1) within the OC population of Jammu and Kashmir, India. The association of each variant was estimated using logistic regression analyses. Out of the 11 SNPs the odds ratio observed for three SNPs; rs2699887 was (1.72 at 95% CI: 1.19–2.48, p = 0.004), rs1695 was (1.87 at 95% CI: 1.28–2.71, p = 0.001), and rs2298881 was (0.66 at 95% CI: 0.46–0.96, p = 0.03) were found significantly associated with the OC after correction with confounding factors i.e. age & BMI. Furthermore, the estimation of interactive analyses was performed and odds ratio observed was 2.44 (1.72–3.47), p value < 0. 001 suggests that there was a strong existence of interplay between the selected genetic variants in OC, which demonstrate that interactive analysis highlights the role of gene–gene interaction that provides an insight among multiple little effects of various polymorphisms in OC.
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