Amphiregulin:: A new growth factor in hepatocarcinogenesis

被引:67
作者
Berasain, C. [1 ]
Castillo, J. [1 ]
Perugorria, M. J. [1 ]
Prieto, J. [1 ]
Avila, M. A. [1 ]
机构
[1] Univ Navarra, CIMA, Div Hepatol & Gene Therapy, Pamplona 31008, Spain
关键词
amphiregulin; proliferation; liver injury; cirrhosis; hepatocarcinoma; carcinogenesis; ALPHA-CONVERTING-ENZYME; RECEPTOR TYROSINE KINASE; WILMS-TUMOR SUPPRESSOR; CELL LUNG-CANCER; HEPATOCELLULAR-CARCINOMA; EGF RECEPTOR; LIVER-REGENERATION; DISTINCT ROLES; RAT-LIVER; HB-EGF;
D O I
10.1016/j.canlet.2007.01.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Amphiregulin (AR) is a member of the epidermal growth factor family and a ligand of the epidermal growth factor receptor (EGFR). As other ligands of the EGFR, AR is synthesized as a precursor that is shed from the plasma membrane by metalloproteases. Hyperactive autocrine loops involving AR production have been described in a variety of tumors, and this growth factor is thought to play a non-redundant role in cancer development. AR expression is not detected in the normal liver, however it is readily induced during acute liver injury and behaves as a potent pro-regenerative and survival factor. Increased AR expression is also detected in human chronic liver injury (liver cirrhosis), which is considered a pre-neoplastic condition. Recent evidences suggest that AR can play a unique role in liver tumorigenesis and in the maintenance of the neoplastic phenotype of hepatocarcinoma cells. In this review, we summarize some aspects of AR patho-biology and the rationale behind its definition as a novel target in hepatocarcinoma therapy. (c) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:30 / 41
页数:12
相关论文
共 87 条
[61]   Frequent epigenetic inactivation of the RASSF1A gene in hepatocellular carcinoma [J].
Schagdarsurengin, U ;
Wilkens, L ;
Steinemann, D ;
Flemming, P ;
Kreipe, HH ;
Pfeifer, GP ;
Schlegelberger, B ;
Dammann, R .
ONCOGENE, 2003, 22 (12) :1866-1871
[62]   Gefitinib, an EGFR inhibitor, prevents hepatocellular carcinoma development in the rat liver with cirrhosis [J].
Schiffer, E ;
Housset, C ;
Cacheux, W ;
Wendum, D ;
Desbois-Mouthon, C ;
Rey, C ;
Clergue, F ;
Poupon, R ;
Barbu, V ;
Rosmorduc, O .
HEPATOLOGY, 2005, 41 (02) :307-314
[63]   Defying death: the hepatocyte's survival kit [J].
Schoemaker, MH ;
Moshage, H .
CLINICAL SCIENCE, 2004, 107 (01) :13-25
[64]   EPIDERMAL GROWTH-FACTOR RECEPTOR-DEPENDENT STIMULATION OF AMPHIREGULIN EXPRESSION IN ANDROGEN-STIMULATED HUMAN PROSTATE-CANCER CELLS [J].
SEHGAL, I ;
BAILEY, J ;
HITZEMANN, K ;
PITTELKOW, MR ;
MAIHLE, NJ .
MOLECULAR BIOLOGY OF THE CELL, 1994, 5 (03) :339-347
[65]   Prostaglandin E2 synergistically enhances receptor tyrosine kinase-dependent signaling system in colon cancer cells [J].
Shao, JY ;
Evers, BM ;
Sheng, HM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (14) :14287-14293
[66]  
Shao JY, 2003, CANCER RES, V63, P5218
[67]   STRUCTURE AND FUNCTION OF HUMAN AMPHIREGULIN - A MEMBER OF THE EPIDERMAL GROWTH-FACTOR FAMILY [J].
SHOYAB, M ;
PLOWMAN, GD ;
MCDONALD, VL ;
BRADLEY, JG ;
TODARO, GJ .
SCIENCE, 1989, 243 (4894) :1074-1076
[68]   AMPHIREGULIN - A BIFUNCTIONAL GROWTH-MODULATING GLYCOPROTEIN PRODUCED BY THE PHORBOL 12-MYRISTATE 13-ACETATE-TREATED HUMAN-BREAST ADENOCARCINOMA CELL-LINE MCF-7 [J].
SHOYAB, M ;
MCDONALD, VL ;
BRADLEY, JG ;
TODARO, GJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (17) :6528-6532
[69]   Autocrine, paracrine and juxtacrine signaling by EGFR ligands. [J].
Singh, AB ;
Harris, RC .
CELLULAR SIGNALLING, 2005, 17 (10) :1183-1193
[70]  
STANDERSON MP, 2006, GROWTH FACTORS, V24, P121