Cell cycle regulation and hepatocarcinogenesis

被引:59
作者
Greenbaum, LE [1 ]
机构
[1] Univ Penn, Sch Med, Dept Med, Div Gastroenterol, Philadelphia, PA 19104 USA
关键词
hepatectomy; regeneration; cell cycle; hepatocellular carcinoma;
D O I
10.4161/cbt.3.12.1392
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma (HCC) develops on a background of chronic hepatitis or cirrhosis. The slow progression of this disease has facilitated the identification of discrete pathologic stages. Increased rates of hepatocyte proliferation in preneoplastic nodules is an early event in the progression of HCC. Increased cell turnover results in the selection of monoclonal hepatocyte populations that subsequently undergo genomic alterations that lead to the development of HCC. The heterogeneous nature of genomic alterations identified in tumors from patients with HCC has impeded the identification of regulatory pathways whose disruption are critical for tumor initiation. However, several regulatory networks important for liver cell proliferation have been characterized using the partial hepatectomy model, an in vivo model of liver cell cycle progression, and are likely relevant to the pathogenesis of hepatocellular carcinoma.
引用
收藏
页码:1200 / 1207
页数:8
相关论文
共 121 条
[1]   TGF-β signaling in cancer -: a double-edged sword [J].
Akhurst, RJ ;
Derynck, R .
TRENDS IN CELL BIOLOGY, 2001, 11 (11) :S44-S51
[2]   Involvement of p21 and p27 in the regulation of CDK activity and cell cycle progression in the regenerating liver [J].
Albrecht, JH ;
Poon, RYC ;
Ahonen, CL ;
Rieland, BM ;
Deng, CX ;
Crary, GS .
ONCOGENE, 1998, 16 (16) :2141-2150
[3]   Regulation of cyclin-dependent kinase inhibitor p21(WAF1/Cip1/Sdi1) gene expression in hepatic regeneration [J].
Albrecht, JH ;
Meyer, AH ;
Hu, MY .
HEPATOLOGY, 1997, 25 (03) :557-563
[4]   Gene expression profiling reveals the mechanism and pathophysiology of mouse liver regeneration [J].
Arai, M ;
Yokosuka, O ;
Chiba, T ;
Imazeki, F ;
Kato, M ;
Hashida, J ;
Ueda, Y ;
Sugano, S ;
Hashimoto, K ;
Saisho, H ;
Takiguchi, M ;
Seki, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (32) :29813-29818
[5]   Met provides essential signals for liver regeneration [J].
Borowiak, M ;
Garratt, AN ;
Wüstefeld, T ;
Strehle, M ;
Trautwein, C ;
Birchmeier, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (29) :10608-10613
[6]   E2F target genes: unraveling the biology [J].
Bracken, AP ;
Ciro, M ;
Cocito, A ;
Helin, K .
TRENDS IN BIOCHEMICAL SCIENCES, 2004, 29 (08) :409-417
[7]   TRANSFORMING GROWTH FACTOR-BETA MESSENGER-RNA INCREASES DURING LIVER-REGENERATION - A POSSIBLE PARACRINE MECHANISM OF GROWTH-REGULATION [J].
BRAUN, L ;
MEAD, JE ;
PANZICA, M ;
MIKUMO, R ;
BELL, GI ;
FAUSTO, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (05) :1539-1543
[8]  
BRAUN L, 1990, CELL GROWTH DIFFER, V1, P103
[9]  
Brenner D, 1998, J GASTROEN HEPATOL, V13, pS93
[10]   DOWN-REGULATION OF TRANSFORMING GROWTH-FACTOR-BETA RECEPTOR TYPE-I, TYPE-II, AND TYPE-III DURING LIVER-REGENERATION [J].
CHARI, RS ;
PRICE, DT ;
SUE, SR ;
MEYERS, WC ;
JIRTLE, RL .
AMERICAN JOURNAL OF SURGERY, 1995, 169 (01) :126-132