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Advisor(s)
Abstract(s)
Persistent high-risk human papillomavirus (HPV)
infection is considered as the central cause of
invasive cervical cancer. Specific HPV 16 and 18
sequence variations were associated with an
increased risk for progression. The purpose of
this study was to analyze intratypic variations of
HPV 16 and 18 within the E6 gene, MY09/11 and
LCR regions, and to evaluate the risk of these
variants for cervical neoplasia among Portuguese
women. Cervical samples from 187 HPV
16-positive and 41 HPV 18-positive women with
normal epithelium, cervical intraepithelial neoplasia,
or invasive cervical cancer were amplified by type-specific PCR, followed by sequence and
phylogenetic analysis. Sixteen new HPV 16 and
18 patterns are described in this paper. European
HPV 16 variants were the most frequent (74.3%),
particularly Ep-T350 (44.4%), followed by African
(16.1%), and Asian-American (9.6%). Non-
European HPV 16 variants were more frequent
in pre-invasive lesions than in normal tissue and
low-grade lesions. However, when analyzed
separately, only African variants were
associated significantly with an increased risk
for cervical cancer. For HPV 18, the AsAi variant
showed a trend, which was not statistically
significant to an enhanced oncogenicity. European
variants seemed to be significantly associated with a lower risk for cervical cancer
development. The distribution of HPV 16 and 18
variants was not related to age or race among
women living in the same geographical region.
Knowledge of variants will be important for risk
determination as well as for designing primers or
probes for HPV detection methods, and for
appropriate cervical cancer prevention strategies.
Description
Keywords
HPV 16 HPV 18 Intratypic Variants Cervical Neoplasia Portugal Infecções Sexualmente Transmissíveis
Pedagogical Context
Citation
J Med Virol. 2007 Dec;79(12):1889-97
