1Senior Research Officer, Department of Molecular Biology & Genetics, Krishna Institute of Medical Sciences “Deemed to be University”, Taluka-Karad, Dist-Satara
2Junior Research Officer, Department of Oncology, Krishna Institute of Medical Sciences “Deemed to be University”, Taluka-Karad, Dist-Satara
3Research Officer, Department of Oncology, Krishna Institute of Medical Sciences “Deemed to be University”, Taluka-Karad, Dist-Satara
4Professor, Department of Oncology, Krishna Institute of Medical Sciences “Deemed to be University”, Taluka-Karad, Dist-Satara
5Medical Oncologist, Department of Oncology, Krishna Institute of Medical Sciences “Deemed to be University”, Taluka-Karad, Dist-Satara
*Corresponding Author: Dr. Kailas D. Datkhile Department of Molecular Biology & Genetics, Krishna Institute of Medical Sciences “Deemed to be University ”Karad, Satara, Maharashtra Tel No: 02164-241555/56, e-mail: hodgeneticslab@kimsuniversity.in
Online published on 23 December, 2019.
Earlier discrepancies in the risk of cervical carcinogenesis due to p53 and p21 genes influenced us to elucidate their association with cervical cancer (CC) in the rural population of south-western Maharashtra.
The hospital based case-control study aimed to investigate association of polymorphisms in p21, p53 genes with risk of CC in Maharashtrian population.
PCR-RFLP method was used to genotype polymorphisms in exon 4 and exon 7 of p53, exon 2 and exon 3 of p21 gene from 350 CC patients and 400 controls.
The variant allele Ser/Ser showed association with increased risk CC as compared to Arg/Arg genotype of codon 249 of p53 whereas codon 72 was not associated risk of CC in rural population. Similarly when we studied C/T and T/T genotypes of exon 3 of p21, T/T genotypes showed significant risk of CC (OR=6.03, 95% CI: 2.63–13.81; p<0.0001).
The findings from this study showed possible association of p53 codon 249 and p21 exon3 polymorphisms with increased risk of cervical carcinogenesis in the women of rural population of Maharashtra.
Cervical Cancer, PCR-RFLP, p53, Genetic Polymorphism