Codon 72 polymorphism of p53 and HPV type 16 E6 variants as risk factors for patients with squamous epithelial lesion of the uterine cervix

被引:13
作者
Burroni, E. [1 ]
Bisanzi, S.
Sani, C.
Puliti, D. [2 ]
Carozzi, F.
机构
[1] ISPO, Unit Analyt & Biomol Cytol, Canc Prevent & Res Inst, I-50139 Florence, Italy
[2] ISPO, Epidemiol Unit, I-50139 Florence, Italy
关键词
HPV; p53; polimorphism; 16; variants; cervical lesions; HUMAN-PAPILLOMAVIRUS TYPE-16; HUMAN-PAPILLOMAVIRUS-16; E6; INTRAEPITHELIAL NEOPLASIA; CANCER; WOMEN; PERSISTENCE; CARCINOMA; PROGRESSION; PREVALENCE; GENOTYPES;
D O I
10.1002/jmv.23417
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Arg/Arg genotype versus Arg/Pro or Pro/Pro at codon 72 of the p53 gene in association with human papillomavirus (HPV) 16 E6 variants has been implicated as a risk marker in cervical neoplasia. However, research on this topic has produced controversial results. The association of p53 codon 72 polymorphism alone and in combination with specific HPV 16 E6 variants with risk of developing squamous intraepithelial cervical lesion has been investigated in low and high-grade squamous intraepithelial lesions and in HPV-negative controls from an Italian population. The data obtained showed statistically significant different distribution of p53 genotypes between healthy controls and precursor lesions, with the p53 arginine homozygous increased in high-grade squamous intraepithelial lesions. The T350G HPV 16 variant was the most frequent variant observed in the analyzed group of Italian women, showing a slight decreasing with the severity of the lesion. At the same time, the number of the prototype T350 slightly increased with the severity of the cytological lesions. In conclusion, p53 arginine homozygous was found to be increased in high-grade lesions, supporting the results of previous investigations indicating that HPV-positive patients with p53 Arg/Arg have an increased risk of developing pre-cancerous lesions. In addition, T350G HPV 16 variant was over-represented in p53 Arg homozygous women with cervical lesions. When p53 genotype and HPV 16 variants are considered together, no difference emerges between cases and controls so is not possible to assess that the oncogenic effect of HPV 16 T350G variant may be influenced by the p53 genotype. J. Med. Virol. 85:8390, 2012. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:83 / 90
页数:8
相关论文
共 57 条
  • [1] Special Report: Policy A review of human carcinogens-Part F: Chemical agents and related occupations
    Baan, Robert
    Grosse, Yann
    Straif, Kurt
    Secretan, Beatrice
    El Ghissassi, Fatiha
    Bouvard, Veronique
    Benbrahim-Tallaa, Lamia
    Guha, Neela
    Freeman, Crystal
    Galichet, Laurent
    Cogliano, Vincent
    [J]. LANCET ONCOLOGY, 2009, 10 (12) : 1143 - 1144
  • [2] IS P53 POLYMORPHISM MAINTAINED BY NATURAL-SELECTION
    BECKMAN, G
    BIRGANDER, R
    SJALANDER, A
    SAHA, N
    HOLMBERG, PA
    KIVELA, A
    BECKMAN, L
    [J]. HUMAN HEREDITY, 1994, 44 (05) : 266 - 270
  • [3] Genome variation of human papillomavirus types: Phylogenetic and medical implications
    Bernard, HU
    Calleja-Macias, IE
    Dunn, ST
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2006, 118 (05) : 1071 - 1076
  • [4] The clinical importance of the nomenclature, evolution and taxonomy of human papillomaviruses
    Bernard, HU
    [J]. JOURNAL OF CLINICAL VIROLOGY, 2005, 32 : S1 - S6
  • [5] Asian-American variants of human papillomavirus 16 and risk for cervical cancer:: a case-control study
    Berumen, J
    Ordoñez, RM
    Lazcano, E
    Salmeron, J
    Galvan, SC
    Estrada, RA
    Yunes, E
    Garcia-Carranca, A
    Madrigal-de la Campa, A
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2001, 93 (17): : 1325 - 1330
  • [6] Haplotype and linkage disequilibrium architecture for human cancer-associated genes
    Bonnen, PE
    Wang, PJ
    Kimmel, M
    Chakraborty, R
    Nelson, DL
    [J]. GENOME RESEARCH, 2002, 12 (12) : 1846 - 1853
  • [7] PREVALENCE OF HUMAN PAPILLOMAVIRUS IN CERVICAL-CANCER - A WORLDWIDE PERSPECTIVE
    BOSCH, FX
    MANOS, MM
    MUNOZ, N
    SHERMAN, M
    JANSEN, AM
    PETO, J
    SCHIFFMAN, MH
    MORENO, V
    KURMAN, R
    SHAH, KV
    ALIHONOU, E
    BAYO, S
    MOKHTAR, HC
    CHICAREON, S
    DAUDT, A
    DELOSRIOS, E
    GHADIRIAN, P
    KITINYA, JN
    KOULIBALY, M
    NGELANGEL, C
    TINTORE, LMP
    RIOSDALENZ, JL
    SARJADI
    SCHNEIDER, A
    TAFUR, L
    TEYSSIE, AR
    ROLON, PA
    TORROELLA, M
    TAPIA, AV
    WABINGA, HR
    ZATONSKI, W
    SYLLA, B
    VIZCAINO, P
    MAGNIN, D
    KALDOR, J
    GREER, C
    WHEELER, C
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (11): : 796 - 802
  • [8] Human papillomavirus type 16 E6 variants in cervical carcinoma: relationship to host genetic factors and clinical parameters
    Brady, CS
    Duggan-Keen, MF
    Davidson, JA
    Varley, JM
    Stern, PL
    [J]. JOURNAL OF GENERAL VIROLOGY, 1999, 80 : 3233 - 3240
  • [9] Genetic Diversity of Human Papillomavirus Type 16 E6, E7, and L1 Genes in Italian Women With Different Grades of Cervical Lesions
    Cento, Valeria
    Ciccozzi, Massimo
    Ronga, Luigi
    Perno, Carlo Federico
    Ciotti, Marco
    [J]. JOURNAL OF MEDICAL VIROLOGY, 2009, 81 (09) : 1627 - 1634
  • [10] Worldwide prevalence and genotype distribution of cervical human papillomavirus DNA in women with normal cytology:: a meta-analysis
    de Sanjose, Silvia
    Diaz, Mireia
    Castellsague, Xavier
    Clifford, Gary
    Bruni, Laia
    Munoz, Nubia
    Bosch, F. Xavier
    [J]. LANCET INFECTIOUS DISEASES, 2007, 7 (07) : 453 - 459