TY - JOUR T1 - Association between p21 Ser31Arg polymorphism and the development of cervical lesion in women infected with high risk HPV. JF - Tumour Biol Y1 - 2016 A1 - Lima, Géssica A1 - Santos, Erinaldo A1 - Angelo, Hildson A1 - Oliveira, Micheline A1 - Heráclio, Sandra A1 - Leite, Fernanda A1 - de Melo, Celso A1 - Crovella, Sergio A1 - Maia, Maria A1 - Souza, Paulo AB -

Infection by high-risk human papillomavirus (HR-HPV) and single nucleotide polymorphism (SNP) in genes involved in cell cycle control, as p21 and p27, are important factors in the development of different types of human cancers. This study aims at investigating whether both the p21 Ser31Arg and p27 V109G polymorphisms are associated with susceptibility to the development of cervical lesions in women HR-HPV positive. We analyzed 132 women HPV positive and with cervical lesions or CC and 154 healthy control (HPV negative and without cervical lesions). p21 Ser31Arg and p27 V109G polymorphisms were analyzed using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method and sequencing. The p21 31Arg allele was associated with susceptibility for the development of cervical lesions (P* = 0.0009), while p27 V109G polymorphism showed no significant differences for this association (P* = 0.89). However, the combined effect of the polymorphisms showed that the presence of the CC genotype (SNP p21 Ser31Arg) conferred protection for the development of cervical lesions (OR = 0.39). p21 Ser31Arg and p27 V109G polymorphisms were not associated with the grade of cervical lesions (CINI, CINII, and CINIII) or CC (P* > 0.05). The HR-HPV more frequent in this study were of 16 (57.6 %) and 18 (37.1 %) types; however, no association was observed when both polymorphisms and risk factors analyzed were compared (P* > 0.05). Our findings suggest a possible association between p21 Ser31tabArg polymorphism and susceptibility to the development of cervical lesions in women from Pernambuco. Brazil.

VL - 37 IS - 8 U1 - http://www.ncbi.nlm.nih.gov/pubmed/26886286?dopt=Abstract ER -