Functional implication of sequence variation in the long control region and E2 gene among human papillomavirus type 18 variants


Por: López-Saavedra A., González-Maya L., Ponce-De-León S., García-Carrancá A., Mohar A., Lizano M.

Publicada: 1 may 2009
Categoría: Virology

Resumen:
Cervical cancer incidence remains highly frequent in developing countries. It is possible that populations of these countries are exposed to more oncogenic human papillomavirus (HPV) variants. Functional differences among high-risk HPV variants have been described, suggesting repercussions on their oncogenic potential. In this report, we demonstrate that the long control region (LCR) of HPV18 variants has distinct transcriptional activities in different cervical cancer cell lines. African (Af)-LCR possessed the lowest transcriptional activity; its sequence harbors the highest number of nucleotide changes among the HPV18 variants analyzed. Some of these embedded in identified transcription-factor-binding sites, suggesting a less aggressive biological activity possibly involved in a slower progression of cervical lesions. Asian-Amerindian LCR showed distinct activities among cell types, while European LCR activity was similar in cell lines tested. Despite multiple nucleotide substitution

Filiaciones:
López-Saavedra A.:
 Univ Nacl Autonoma Mexico, Biomed Res Inst, Mexico City 14080, DF, Mexico

González-Maya L.:
 College of Pharmacy, Autonomous University of Morelos, Cuernavaca, Mexico

Ponce-De-León S.:
 Clinical Epidemiology Unit, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico

García-Carrancá A.:
 Univ Nacl Autonoma Mexico, Biomed Res Inst, Mexico City 14080, DF, Mexico

Mohar A.:
 Univ Nacl Autonoma Mexico, Biomed Res Inst, Mexico City 14080, DF, Mexico

Lizano M.:
 Univ Nacl Autonoma Mexico, Biomed Res Inst, Mexico City 14080, DF, Mexico
ISSN: 03048608
Editorial
Springer-Verlag, SACHSENPLATZ 4-6, PO BOX 89, A-1201 WIEN, AUSTRIA, Austria
Tipo de documento: Article
Volumen: 154 Número: 5
Páginas: 747-754
WOS Id: 000265915300002
ID de PubMed: 19337781