a new, effective and high-yield approach for identifying liver tumor suppressors一个新的、有效和高收益的方法识别肝肿瘤的抑制.pdfVIP
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a new, effective and high-yield approach for identifying liver tumor suppressors一个新的、有效和高收益的方法识别肝肿瘤的抑制
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Esra Olgun* and Lewis R Roberts†
Addresses: *Department of Internal Medicine, McLaren Regional Medical Center, 401 S Ballenger Highway, Flint, Michigan 48532, USA.
†Miles and Shirley Fiterman Center for Digestive Diseases, College of Medicine, Mayo Clinic, 200 First Street SW, Rochester,
Minnesota 55905, USA.
Correspondence: Lewis R Roberts. Email: roberts.lewis@
Published: 26 February 2009
Genome Medicine 2009, 11::26 (doi:10.1186/gm26)
The electronic version of this article is the complete one and can be
found online at /content/1/2/26
© 2009 BioMed Central Ltd
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Despite recent advances in research in hepatocarcinogenesis, we still lack a comprehensive view
of the major pathways involved in liver carcinogenesis. Current concepts suggest that a limited
number of molecular alterations involving oncogene activation and tumor suppressor inhibition
are responsible for initiation of cancer. A recent publication by Zender et al. utilizes a combi-
nation of high-resolution comparative genomic hybridization, short hairpin RNA inhibition of
target genes at the locations of focal genomic deletions, and a primed cell mosaic mouse model to
identify novel tumor suppressors in hepatocellular carcinoma. This exciting new model promises
to provide additional insights into the mechanisms of carcinogenesis.
IInnttrroodduuccttiioonn the inherent ability to activate tumor suppressor genes or
Hepatocellular carcinoma (HCC) is the fifth most common pathways through oncogene-induced apop
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