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Transposon mutagenesis identifies genes driving hepatocellular carcinoma in a chronic hepatitis B mouse model.

Bard-Chapeau, Emilie A (author)
Nguyen, Anh-Tuan (author)
Rust, Alistair G (author)
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Sayadi, Ahmed (author)
Institute of Molecular and Cell Biology, Singapore, Singapore
Lee, Philip (author)
Chua, Belinda Q (author)
New, Lee-Sun (author)
de Jong, Johann (author)
Ward, Jerrold M (author)
Chin, Christopher K Y (author)
Chew, Valerie (author)
Toh, Han Chong (author)
Abastado, Jean-Pierre (author)
Benoukraf, Touati (author)
Soong, Richie (author)
Bard, Frederic A (author)
Dupuy, Adam J (author)
Johnson, Randy L (author)
Radda, George K (author)
Chan, Eric Chun Yong (author)
Wessels, Lodewyk F A (author)
Adams, David J (author)
Jenkins, Nancy A (author)
Copeland, Neal G (author)
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 (creator_code:org_t)
2013-12-08
2014
English.
In: Nature Genetics. - : Springer Science and Business Media LLC. - 1061-4036 .- 1546-1718. ; 46:1
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The most common risk factor for developing hepatocellular carcinoma (HCC) is chronic infection with hepatitis B virus (HBV). To better understand the evolutionary forces driving HCC, we performed a near-saturating transposon mutagenesis screen in a mouse HBV model of HCC. This screen identified 21 candidate early stage drivers and a very large number (2,860) of candidate later stage drivers that were enriched for genes that are mutated, deregulated or functioning in signaling pathways important for human HCC, with a striking 1,199 genes being linked to cellular metabolic processes. Our study provides a comprehensive overview of the genetic landscape of HCC.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

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