Molecular Mechanisms of Hepatocellular Carcinoma

被引:538
作者
Aravalli, Rajagopal N. [1 ]
Steer, Clifford J. [2 ,3 ]
Cressman, Erik N. K. [1 ]
机构
[1] Univ Minnesota, Sch Med, Dept Radiol, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Dept Med, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Sch Med, Dept Genet Cell Biol & Dev, Minneapolis, MN 55455 USA
关键词
D O I
10.1002/hep.22580
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatocellular carcinoma (HCC) typically has poor prognosis, because it is often diagnosed at an advanced stage. Heterogeneous phenotypic and genetic traits of affected individuals and a wide range of risk factors have classified it a complex disease. HCC is not amenable to standard chemotherapy and is resistant to radiotherapy. In most cases, surgical resection and liver transplantation remain the only curative treatment options. Therefore, development of novel, effective therapies is of prime importance. Extensive research over the past decade has identified a number of molecular biomarkers as well as cellular networks and signaling pathways affected in liver cancer. Recent studies using a combination of "omics" technologies, microRNA studies, combinatorial chemistry, and bioinformatics are providing new insights into the gene expression and protein profiles during various stages of the disease. In this review, we discuss the contribution of these newer approaches toward an understanding of molecular mechanisms of HCC and for the development of novel cancer therapeutics. (HEPATOLOGY 2008;48:2047-2063.)
引用
收藏
页码:2047 / 2063
页数:17
相关论文
共 201 条
[1]   The clinical applications of a systems approach [J].
Ahn, Andrew C. ;
Tewari, Muneesh ;
Poon, Chi-Sang ;
Phillips, Russell S. .
PLOS MEDICINE, 2006, 3 (07) :956-960
[2]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[3]   Cell differentiation - Hepatocytes from nonhepatic adult stem cells [J].
Alison, MR ;
Poulsom, R ;
Jeffery, R ;
Dhillon, AP ;
Quaglia, A ;
Jacob, J ;
Novelli, M ;
Prentice, G ;
Williamson, J ;
Wright, NA .
NATURE, 2000, 406 (6793) :257-257
[4]   Immortalization of a primate bipotent epithelial liver stem cell [J].
Allain, JE ;
Dagher, I ;
Mahieu-Caputo, D ;
Loux, N ;
Andreoletti, M ;
Westerman, K ;
Briand, P ;
Franco, D ;
Leboulch, P ;
Weber, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (06) :3639-3644
[5]   In vivo contribution of murine mesenchymal stem cells into multiple cell-types under minimal damage conditions [J].
Anjos-Afonso, F ;
Siapati, EK ;
Bonnet, D .
JOURNAL OF CELL SCIENCE, 2004, 117 (23) :5655-5664
[6]   Disruption of the p16/cyclin D1/retinoblastoma protein pathway in the majority of human hepatocellular carcinomas [J].
Azechi, H ;
Nishida, N ;
Fukuda, Y ;
Nishimura, T ;
Minata, M ;
Katsuma, H ;
Kuno, M ;
Ito, T ;
Komeda, T ;
Kita, R ;
Takahashi, R ;
Nakao, K .
ONCOLOGY, 2001, 60 (04) :346-354
[7]  
Baba M, 1997, INT J CANCER, V72, P815, DOI 10.1002/(SICI)1097-0215(19970904)72:5<815::AID-IJC18>3.3.CO
[8]  
2-N
[9]   Codon 64 of K-ras gene mutation pattern in hepatocellular carcinomas induced by bleomycin and 1-nitropyrene in A/J mice [J].
Bai, F ;
Nakanishi, Y ;
Takayama, K ;
Pei, XH ;
Inoue, K ;
Harada, T ;
Izumi, M ;
Hara, N .
TERATOGENESIS CARCINOGENESIS AND MUTAGENESIS, 2003, :161-170
[10]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29