MicroRNA involvement in hepatocellular carcinoma

被引:224
作者
Gramantieri, Laura [1 ]
Fornari, Francesca [1 ]
Callegari, Elisa [2 ]
Sabbioni, Silvia [2 ]
Lanza, Giovanni [2 ]
Croce, Carlo M. [2 ,3 ]
Bolondi, Luigi [1 ]
Negrini, Massimo [2 ]
机构
[1] Univ Bologna, Dept Internal Med & Gastroenterol, Bologna, Italy
[2] Univ Ferrara, Dept Expt & Diagnost Med, I-44100 Ferrara, Italy
[3] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
关键词
microRNA; hepatocellular carcinoma; diagnosis; therapy;
D O I
10.1111/j.1582-4934.2008.00533.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hepatocellular carcinoma (HCC) is the third cause of cancer-related death worldwide. Curative options for HCC are limited and exclusively available for patients carrying an early stage HCC. In advanced stages, traditional chemotherapy proved to be only marginally effective or even toxic. Thus, the identification of new treatment options is needed. New targets for non-conventional treatment will necessarily take advantage of progresses on the molecular pathogenesis of HCC. MicroRNAs (miRNAs) are a group of tiny RNAs with a fundamental role in the regulation of gene expression. Aberrant expression of several miRNAs was found to be involved in human hepatocarcinogenesis. miRNA expression signatures were correlated with bio-pathological and clinical features of HCC. In some cases, aberrantly expressed miRNAs could be linked to cancer-associated pathways, indicating a direct role in liver tumourigenesis. For example, up-regulation of mir-221 and mir-21 could promote cell cycle progression, reduce cell death and favour angiogenesis and invasion. These findings suggest that miRNAs could become novel molecular targets for HCC treatment. The demonstration of in vivo efficacy and safety of anti-miRNA compounds has opened the way to their use in clinical trials.
引用
收藏
页码:2189 / 2204
页数:16
相关论文
共 166 条
[51]   Reduced stability of retinoblastoma protein by gankyrin, an oncogenic ankyrin-repeat protein overexpressed in hepatomas [J].
Higashitsuji, H ;
Itoh, K ;
Nagao, T ;
Dawson, S ;
Nonoguchi, K ;
Kido, T ;
Mayer, RJ ;
Arii, S ;
Fujita, J .
NATURE MEDICINE, 2000, 6 (01) :96-99
[52]  
Hirohashi K, 2004, HEPATO-GASTROENTEROL, V51, P1121
[53]   Growth factor receptors and related signalling pathways as targets for novel treatment strategies of hepatocellular cancer [J].
Hoepfner, Michael ;
Schuppan, Detlef ;
Scheruebl, Hans .
WORLD JOURNAL OF GASTROENTEROLOGY, 2008, 14 (01) :1-14
[54]   The microRNAs miR-373 and miR-520c promote tumour invasion and metastasis [J].
Huang, Qihong ;
Gumireddy, Kiranmai ;
Schrier, Mariette ;
Le Sage, Carlos ;
Nagel, Remco ;
Nair, Suresh ;
Egan, David A. ;
Li, Anping ;
Huang, Guanghua ;
Klein-Szanto, Andres J. ;
Gimotty, Phyllis A. ;
Katsaros, Dionyssios ;
Coukos, George ;
Zhang, Lin ;
Pure, Ellen ;
Agami, Reuven .
NATURE CELL BIOLOGY, 2008, 10 (02) :202-U83
[55]   Hepatology - Microarray analysis of microRNA expression in hepatocellular carcinoma and non-tumorous tissues without viral hepatitis [J].
Huang, Yuan-Shuai ;
Dai, Yong ;
Yu, Xiao-Fang ;
Bao, Shi-Yun ;
Yin, Yi-Bing ;
Tang, Min ;
Hu, Cheng-Xiao .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2008, 23 (01) :87-94
[56]  
Iguchi H, 2002, J EXP CLIN CANC RES, V21, P309
[57]  
Iizuka N, 2002, CANCER RES, V62, P3939
[58]   Oligonucleotide microarray for prediction of early intrahepatic recurrence of hepatocellular carcinoma after curative resection [J].
Iizuka, N ;
Oka, M ;
Yamada-Okabe, H ;
Nishida, M ;
Maeda, Y ;
Mori, N ;
Takao, T ;
Tamesa, T ;
Tangoku, A ;
Tabuchi, H ;
Hamada, K ;
Nakayama, H ;
Ishitsuka, H ;
Miyamoto, T ;
Hirabayashi, A ;
Uchimura, S ;
Hamamoto, Y .
LANCET, 2003, 361 (9361) :923-929
[59]   MicroRNA signatures in human ovarian cancer [J].
Iorio, Marilena V. ;
Visone, Rosa ;
Di Leva, Gianpiero ;
Donati, Valentina ;
Petrocca, Fabio ;
Casalini, Patrizia ;
Taccioli, Cristian ;
Volinia, Stefano ;
Liu, Chang-Gong ;
Alder, Hansjuerg ;
Calin, George A. ;
Menard, Sylvie ;
Croce, Carlo M. .
CANCER RESEARCH, 2007, 67 (18) :8699-8707
[60]   MicroRNA gene expression deregulation in human breast cancer [J].
Iorio, MV ;
Ferracin, M ;
Liu, CG ;
Veronese, A ;
Spizzo, R ;
Sabbioni, S ;
Magri, E ;
Pedriali, M ;
Fabbri, M ;
Campiglio, M ;
Ménard, S ;
Palazzo, JP ;
Rosenberg, A ;
Musiani, P ;
Volinia, S ;
Nenci, I ;
Calin, GA ;
Querzoli, P ;
Negrini, M ;
Croce, CM .
CANCER RESEARCH, 2005, 65 (16) :7065-7070