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https://doi.org/10.1038/aps.2010.94
Title: | Chromosome 1q21 amplification and oncogenes in hepatocellular carcinoma | Authors: | Chen, L Chan, T.H.M Guan, X.-Y |
Keywords: | caspase 3 caspase 9 cyclic AMP dependent protein kinase regulatory subunit Ibeta cyclic AMP responsive element binding protein amplicon apoptosis binding affinity cancer growth cancer therapy cell cycle progression cell cycle regulation cell proliferation chromosome 13q chromosome 16p chromosome 17p chromosome 17q chromosome 1q chromosome 20q chromosome 4q chromosome 6q chromosome 8p chromosome aberration comparative genomic hybridization copy number variation distant metastasis drug inhibition gene amplification gene loss gene overexpression gene targeting gene translocation genetic gain genetic transfection human liver carcinogenesis liver cell carcinoma minimal amplified region nonhuman oncogene real time polymerase chain reaction review single nucleotide polymorphism Animals Carcinoma, Hepatocellular Chromosomes, Human, Pair 1 DNA Helicases DNA-Binding Proteins Gene Amplification Humans Oncogenes |
Issue Date: | 2010 | Publisher: | Wiley | Citation: | Chen, L, Chan, T.H.M, Guan, X.-Y (2010). Chromosome 1q21 amplification and oncogenes in hepatocellular carcinoma. Acta Pharmacologica Sinica 31 (9) : 1165-1171. ScholarBank@NUS Repository. https://doi.org/10.1038/aps.2010.94 | Rights: | Attribution 4.0 International | Abstract: | Hepatocellular carcinoma (HCC) is among the most lethal of human malignancies. During human multistep hepatocarcinogenesis, genomic gain represents an important mechanism in the activation of proto-oncogenes. In many circumstances, activated oncogenes hold clinical implications both as prognostic markers and targets for cancer therapeutics. Gain of chromosome 1q copy is one of the most frequently detected alterations in HCC and 1q21 is the most frequent minimal amplifying region (MAR). A better understanding of the physiological and pathophysiological roles of target genes within 1q21 amplicon will significantly improve our knowledge in HCC pathogenesis, and may lead to a much more effective management of HCC bearing amplification of 1q21. Such knowledge has long term implications for the development of new therapeutic strategies for HCC treatment. Our research group and others, focused on the identification and characterization of 1q21 target genes such as JTB, CKS1B, and CHD1L in HCC progression. In this review, we will summarize the current scientific knowledge of known target genes within 1q21 amplicon and the precise oncogenic mechanisms of CHD1L will be discussed in detail. © 2010 CPS and SIMM All rights reserved. | Source Title: | Acta Pharmacologica Sinica | URI: | https://scholarbank.nus.edu.sg/handle/10635/178197 | ISSN: | 1671-4083 | DOI: | 10.1038/aps.2010.94 | Rights: | Attribution 4.0 International |
Appears in Collections: | Staff Publications Elements |
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