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Interaction between glutathione-S-transferase polymorphisms, smoking habit, and HPV infection in cervical cancer risk

TitleInteraction between glutathione-S-transferase polymorphisms, smoking habit, and HPV infection in cervical cancer risk
Publication TypeArticolo su Rivista peer-reviewed
Year of Publication2010
AuthorsPalma, S., Novelli Flavia, Padua L., Venuti A., Prignano G., Mariani L., Cozzi R., Tirindelli D., and Testa Antonella
JournalJournal of Cancer Research and Clinical Oncology
Volume136
Pagination1101-1109
ISSN01715216
Keywordsadult, aged, article, blood sampling, cancer risk, Caucasian, Cohort studies, controlled study, DNA extraction, DNA isolation, Female, gene frequency, Genetic, Genetic polymorphism, genotype, Glutathione S-Transferase pi, Glutathione Transferase, glutathione transferase M1, glutathione transferase P1, glutathione transferase T1, human, human cell, human tissue, Humans, major clinical study, Middle Aged, papillomavirus infection, Papillomavirus Infections, Polymerase Chain Reaction, Polymorphism, priority journal, restriction fragment length polymorphism, Risk Factors, Smoking, smoking habit, squamous epithelium, Uterine Cervical Neoplasms, uterine cervix cancer, uterine cervix carcinoma in situ, young adult
Abstract

Purpose: Human papillomavirus (HPV) infection is considered the major cause of cervical cancer (CC), but a number of infected women do not develop invasive lesions, suggesting the role of genetic susceptibility and environmental co-factors for cancer outbreak. The aim of this study was to investigate whether some GST polymorphisms could influence the risk to develop CC, either by themselves or in combination with smoking habit, in a cohort of high-risk HPV (HR-HPV) infected Italian women. Methods: The study population comprises 192 Italian women including 81 HR-HPV infected women bearing cervical lesions and 111 healthy controls. The cases include: 26 low-grade squamous intraepithelial lesions (LSILs), 30 high-grade-SIL, and 25 CCs, while controls were all negative for HPV. DNA was extracted from peripheral blood samples or cytobrush and individuals were genotyped for GSTM1, GSTT1, and GSTP1 polymorphisms using PCR and PCR/RFLP techniques. Results: On studying the association of GSTs gene polymorphisms with cervical cancer lesions, the combination of GSTM1 null, GSTT1 null and GSTP1 AA genotypes, independently on smoking habit, seems to be related to a 5.7-fold increased risk of developing CLs with a considerable statistical significance (P = 0.0091). Conclusions: We suggest that the investigation of multiple gene polymorphisms, versus single genes, could contribute to a better understanding of the effect of susceptibility genes on cancer risk. © 2010 Springer-Verlag.

Notes

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URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-77953233155&doi=10.1007%2fs00432-009-0757-3&partnerID=40&md5=40332a445e76b9b8974111b429b49156
DOI10.1007/s00432-009-0757-3
Citation KeyPalma20101101