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01 · ABSTRACT

Abstract

The aim was to determine the association between R72P polymorphism of p53 gene and the risk of developing squamous intraepithelial cervical lesions in HPV-16 and /or 18 infected women. Two groups of women were included in this study: 74 patients HPV-16 and /or 18 positive with a cytological and colposcopy diagnosis of squamous intraepithelial lesion and a group of unrelated 130 healthy blood-donors. The viral genotype, allele and genotype of the polymorphism frequencies were determined by PCR approached. The results were analyzed with the statistical programs DeFinetti and STAT intercooled v11.1. Patients with high-grade squamous intrahepitelial lesions (HG-SIL) were infected mainly by HPV-16 (60.72%) compared to low-grade lesions (LG-SIL) (39.28%) (OR 3.14; p= 0.037), with HPV-18 genotype 68.96% of LG-SIL and 31.04% were HG-SIL (OR=0.24, p=0.006). HG-SIL were more common in patients carrying both viral genotypes (70.59% vs 29.41%) (OR 2.8, p = 0.008). A statistically significant association was observed between the genotype R/R and HG-SIL (OR=11.25, IC 3.8-33.29, p= 0.000) compared to those with LG-SIL. The P/R genotype was significantly more frequent in patients LG-SIL, compared to HG-SIL (OR=0.27, p=0.00). In conclusion patients with the R/R genotype showed more susceptibility to HPV-16 infection and they have almost 12 times more risk probability of HG-SIL compared to women having the heterozygous genotype and HPV-18.

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02 · OJS METADATA

Keywords

Human papillomavirusp53 geneR72P polymorphismcervical cancer
03 · PUBLICATION RECORD

Article details

JournalMedical Research Archives
IssueVol 3 No 8 (2016): Vol.3 Issue 8
SectionResearch Articles
Published05 April 2016
ISSN2375-1924
04 · RIGHTS & REUSE

Rights & reuse

This article is published under a Creative Commons Attribution License (CC BY 3.0) and may be shared or distributed by anyone as long as attribution is given to the journal.

Authors & affiliations

JR

Juan Jose Rios-Tostado

Escuela de Biologia, Universidad Autonoma de Sinaloa. Av. de Las Americas y Boulevard Universitarios, Culiacan, Sinaloa 80010

JV

Jesus Salvador Velarde-Felix

Escuela de Biologia, Universidad Autonoma de Sinaloa. Av. de Las Americas y Boulevard Universitarios, Culiacan, Sinaloa 80010

IO

Ignacio Osuna-Ramirez

Posgrado en Ciencias Biomedicas, Facultad de Ciencias Quimico Biologicas, Universidad Autonoma de Sinaloa. Av. de Las Americas y Boulevard Universitarios, Culiacan, Sinaloa 80010

HC

Hipolito Castillo-Ureta

Escuela de Biologia, Universidad Autonoma de Sinaloa. Av. de Las Americas y Boulevard Universitarios, Culiacan, Sinaloa, 80010

RM

Rocio Susana Mendez-Martinez

Laboratorio de Virus y Cancer, Instituto Nacional de Cancerologia, Ignacio Allende esquina de Tlalpan, Belisario Dominguez Secc. 16, 14080 Ciudad de Mexico

LO

Lorenzo Ulises Osuna-Martinez

Posgrado en Ciencias Biomedicas, Facultad de Ciencias Quimico Biologicas, Universidad Autonoma de Sinaloa. Av. de Las Americas y Boulevard Universitarios, Culiacan, Sinaloa, 80010.

HL

Hector Samuel Lopez-Moreno

Posgrado en Ciencias Biomedicas, Facultad de Ciencias Quimico Biologicas, Universidad Autonoma de Sinaloa. Av. de Las Americas y Boulevard Universitarios, Culiacan, Sinaloa, 80010

FM

Fred Morgan-Ortiz

Centro de Investigacion y Docencia en Ciencias de la Salud, Av. Alvaro Obregón 1422, Tierra Blanca, 80030 Culiacan, Sinaloa

JM

Joel Murillo-Llanez

5Departamento de Investigación, Hospital de la Mujer, Blvd. Miguel Tamayo, Desarrollo Urbano Tres Ríos, Culiacán, Sinaloa, 80020 México

JR

Jose Guadalupe Rendon

Facultad de Ciencias Quimico Biologicas Universidad Autonoma de Sinaloa Av. de Las Americas y Boulevard Universitarios Culiacan, Sinaloa 80010

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