Association of TAP Gene Polymorphisms and Risk of Cervical Intraepithelial Neoplasia. Issue 2 (28th July 2013)

• Record Type: Journal Article
• Authors: Natter, Camilla; Polterauer, Stephan; Rahhal-Schupp, Jasmin; Cacsire Castillo-Tong, Dan; Pils, Sophie; Speiser, Paul; Zeillinger, Robert; Heinze, Georg; Grimm, Christoph
• Other Names: Srivastava Sudhir Academic Editor.
• Is Part Of: Disease markers. Volume 35:Issue 2(2013)
• Page Start: 79
• Page End: 84
• Publication Date: 2013-07-28
• Subjects: Diagnosis -- Periodicals; Biochemical markers -- Periodicals; Pathology -- Periodicals; 616
• DOI: 10.1155/2013/368732
• Languages: English
• ISSNs: 0278-0240

Abstract

Abstract : Background. Transporter associated with antigen processing (TAP) is responsible for peptide loading onto class I major histocompatibility complex (MHC-I) molecules. TAP seems to facilitate the detection of HPV by MHC-I molecules and contributes to successful eradication of HPV. TAP polymorphisms could have an important impact on the course of HPV infection. Objective. The aim of this study is to evaluate the association between five TAP gene polymorphisms and the risk of CIN. Methods. This case-control study investigated five common TAP polymorphisms in TAP1 (1341 and 2254) and TAP2 (1135, 1693, and 1993) in 616 women with CIN and 206 controls. Associations between gene polymorphisms and risk of CIN were analysed by univariate and multivariable models. The combined effect of the five TAP gene polymorphisms on the risk for CIN was investigated by haplotype analysis. Results. No significant difference in genotype distribution of the five TAP polymorphisms was observed in women with CIN and controls. Haplotype analysis revealed that women with haplotype mut-wt-wt-wt-wt (TAP polymorphisms t1135-t1341-t1693-t1993-t2254) had a significantly lower risk for CIN, compared to women with the haplotype wt-wt-wt-wt-wt (P = 0.006 ; OR 0.5 [0.35 – 0.84 ]). Conclusion. Identification of this haplotype combination could be used to identify women, less susceptible for development of CIN following HPV infection.