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Gene network reconstruction reveals cell cycle and antiviral genes as major drivers of cervical cancer

Although human papillomavirus (HPV) was identified as an etiological factor in cervical cancer, the key human gene drivers of this disease remain unknown. Here we apply an unbiased approach integrating gene expression and chromosomal aberration data. In an independent group of patients, we reconstru...

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Detalles Bibliográficos
Autores principales: Mine, Karina L., Shulzhenko, Natalia, Yambartsev, Anatoly, Rochman, Mark, Sanson, Gerdine F. O., Lando, Malin, Varma, Sudhir, Skinner, Jeff, Volfovsky, Natalia, Deng, Tao, Brenna, Sylvia M. F., Carvalho, Carmen R. N., Ribalta, Julisa C. L., Bustin, Michael, Matzinger, Polly, Silva, Ismael D. C. G., Lyng, Heidi, Gerbase-DeLima, Maria, Morgun, Andrey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237593/
https://www.ncbi.nlm.nih.gov/pubmed/23651994
http://dx.doi.org/10.1038/ncomms2693
Descripción
Sumario:Although human papillomavirus (HPV) was identified as an etiological factor in cervical cancer, the key human gene drivers of this disease remain unknown. Here we apply an unbiased approach integrating gene expression and chromosomal aberration data. In an independent group of patients, we reconstruct and validate a gene regulatory meta-network, and identify cell cycle and antiviral genes that constitute two major sub-networks up-regulated in tumour samples. These genes are located within the same regions as chromosomal amplifications, most frequently on 3q. We propose a model in which selected chromosomal gains drive activation of antiviral genes contributing to episomal virus elimination, which synergizes with cell cycle dysregulation. These findings may help to explain the paradox of episomal HPV decline in women with invasive cancer who were previously unable to clear the virus.