Evidence map›Paper›PMID 41415141›Full record

ArticleJournal of mid-life health

Association between NAD (P) H: Quinone Oxidoreductase 1 C609T Gene Polymorphism and Risk Factors in Cases of Cervical Cancer in Indian Women.

Sangeeta Kumari, Shuchi Agrawal, Nitu Nigam, Nisha Singh, Sudhir Singh, Praveen Kumar, Avinash Agrawal

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Article in Journal of mid-life health. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Sangeeta KumariDepartment of Obstetrics and Gynaecology, King Georges Medical University, Lucknow, Uttar Pradesh, India.
Shuchi AgrawalDepartment of Obstetrics and Gynaecology, King Georges Medical University, Lucknow, Uttar Pradesh, India.
Nitu NigamDepartment of CFAR, Centre for Advanced Research.
Nisha SinghDepartment of Obstetrics and Gynaecology, King Georges Medical University, Lucknow, Uttar Pradesh, India.
Sudhir SinghDepartment of Radiotherapy, King Georges Medical University, Lucknow, Uttar Pradesh, India.
Praveen KumarDepartment of CFAR, Centre for Advanced Research King Georges Medical University, Lucknow, Uttar Pradesh, India.
Avinash AgrawalDepartment of Critical Care Medicine, King Georges Medical University, Lucknow, Uttar Pradesh, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: HPV infection is causative agent for cervical cancer, majority of HPV infections are low-grade, self-limited, and revert spontaneously in some HPV infection fails to clear this hints towards presence of certain genetic factors which predispose them to increase risk of pre-cancer and cancer. We aimed to investigate the factors which have bearing on rising cancer cases in India and to elucidate the genetic susceptibility distribution of NAD (P) H: quinone oxidoreductase 1 C609T gene polymorphism. Materials and Methods: Study recruited 142 women with biopsy-proven cervical cancer (the case group) and 142 women with normal cytology (the control group). DNA extracted from blood via QIAamp DNA mini kit. The DNA of each participant was amplified and the genotype and allelic frequency were compared. Results: In our study, maximum women in the case group had stage II (69.7%) squamous cell carcinoma (97.2%). 75.4% of the cases had moderately differentiated carcinoma and had no treatment before (43.7%). Among cases, the prevalence of genotype CC, CT and TT was 42.3%, 19.7% and 38.0%, respectively compared to 54.9%, 13.4% and 31.7%, in controls. The odds of having CC (odds ratio [OR] =0.64; 95% confidence interval [CI] =0.38-1.08), CC or CT in contrast to TT (OR = 0.756; 95% CI = 0.46-1.23), CC in contrast to TT/CT (OR = 0.694; 95% CI = 0.44-1.10) was lesser in cases compared to the controls, while Odds of allele T as compared to C were significantly elevated in cases as compared to that in the controls (OR = 1.48; 95% CI = 1.06-2.06). The proportion of TT genotype was elevated in advanced stages as compared to early stages. Conclusion: We found the odds of allele T as compared to C were markedly elevated in cases as compared to controls.

Indexed as

Cervical cancergene polymorphismNAD (P) H: quinone oxidoreductase 1single nucleotide polymorphism

Identifiers

PMID41415141
PMCPMC12711174

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