Author
Listed:
- Karina L. Mine
(Instituto de Imunogenética—Associação Fundo de Incentivo à Pesquisa (IGEN-AFIP)
Universidade Federal de São Paulo)
- Natalia Shulzhenko
(Instituto de Imunogenética—Associação Fundo de Incentivo à Pesquisa (IGEN-AFIP)
Laboratory of Cellular and Molecular Immunology, NIAID, NIH
College of Pharmacy, Oregon State University)
- Anatoly Yambartsev
(Institute of Mathematics and Statistics, University of Sao Paulo)
- Mark Rochman
(Protein Section, Laboratory of Metabolism, Center for Cancer Research, NCI, NIH
Present address: Division of Allergy and Immunology, Cincinnati Children’s Hospital, Cincinnati, Ohio, USA (G.F.O.S.); Instituto de Ciências da Saúde, Universidade Federal de Mato Grosso - Campus Sinop, Sinop, Mato Grosso, Brazil (M.R.))
- Gerdine F. O. Sanson
(Instituto de Imunogenética—Associação Fundo de Incentivo à Pesquisa (IGEN-AFIP)
Present address: Division of Allergy and Immunology, Cincinnati Children’s Hospital, Cincinnati, Ohio, USA (G.F.O.S.); Instituto de Ciências da Saúde, Universidade Federal de Mato Grosso - Campus Sinop, Sinop, Mato Grosso, Brazil (M.R.))
- Malin Lando
(Norwegian Radium Hospital)
- Sudhir Varma
(Bioinformatics and Computational Biosciences Branch, NIAID, NIH)
- Jeff Skinner
(Bioinformatics and Computational Biosciences Branch, NIAID, NIH)
- Natalia Volfovsky
(Advanced Biomedical Computing Center, SAIC-Frederick, Inc)
- Tao Deng
(Protein Section, Laboratory of Metabolism, Center for Cancer Research, NCI, NIH)
- Sylvia M. F. Brenna
(Medical School of Universidade Cidade de São Paulo (UNICID))
- Carmen R. N. Carvalho
(Universidade Federal de São Paulo)
- Julisa C. L. Ribalta
(Universidade Federal de São Paulo)
- Michael Bustin
(Protein Section, Laboratory of Metabolism, Center for Cancer Research, NCI, NIH)
- Polly Matzinger
(Laboratory of Cellular and Molecular Immunology, NIAID, NIH)
- Ismael D. C. G. Silva
(Universidade Federal de São Paulo)
- Heidi Lyng
(Norwegian Radium Hospital)
- Maria Gerbase-DeLima
(Instituto de Imunogenética—Associação Fundo de Incentivo à Pesquisa (IGEN-AFIP)
Universidade Federal de São Paulo)
- Andrey Morgun
(Instituto de Imunogenética—Associação Fundo de Incentivo à Pesquisa (IGEN-AFIP)
Laboratory of Cellular and Molecular Immunology, NIAID, NIH
College of Pharmacy, Oregon State University)
Abstract
Although human papillomavirus was identified as an aetiological 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 subnetworks upregulated 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 human papillomavirus decline in women with invasive cancer who were previously unable to clear the virus.
Suggested Citation
Karina L. Mine & Natalia Shulzhenko & Anatoly Yambartsev & Mark Rochman & Gerdine F. O. Sanson & Malin Lando & Sudhir Varma & Jeff Skinner & Natalia Volfovsky & Tao Deng & Sylvia M. F. Brenna & Carmen, 2013.
"Gene network reconstruction reveals cell cycle and antiviral genes as major drivers of cervical cancer,"
Nature Communications, Nature, vol. 4(1), pages 1-11, June.
Handle:
RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms2693
DOI: 10.1038/ncomms2693
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