microRNA Involvement in Hepatocellular Carcinoma

被引:83
作者
Negrini, Massimo [1 ]
Gramantieri, Laura [2 ]
Sabbioni, Silvia [1 ]
Croce, Carlo M. [1 ,3 ]
机构
[1] Univ Ferrara, Dept Expt & Diagnost Med, I-44121 Ferrara, Italy
[2] Univ Bologna, Dept Internal Med & Gastroenterol, Bologna, Italy
[3] Ohio State Univ, Dept Mol Virol Immunol & Med Genet, Ctr Comprehens Canc, Columbus, OH 43210 USA
关键词
microRNA; hepatocellular carcinoma; diagnosis; therapy; HEPATITIS-C VIRUS; ESTROGEN-RECEPTOR-ALPHA; ENDOTHELIAL GROWTH-FACTOR; GENE-EXPRESSION PROFILES; P53; TUMOR-SUPPRESSOR; ANTISENSE CYCLIN G1; HUMAN BREAST-CANCER; CELL-DEATH; DOWN-REGULATION; B-VIRUS;
D O I
10.2174/187152011796011037
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The role of microRNAs (miRNAs) in human tumorigenesis has been demonstrated by gene profiling and functional studies. In hepatocellular carcinoma (HCC), consistently deregulated miRNAs were identified. Their aberrant expression revealed relations shared with other types of cancer and others unique to HCC, namely the down-regulation of miR-122. Most importantly, functional and molecular studies uncovered mechanisms that linked deregulated miRNAs to cancer-associated pathways, thereby placing their deregulation in a more rational framework. These results improved our knowledge concerning the molecular basis of HCC and helped to increase our understanding about the great clinical potential behind these small molecules. In fact, a number of studies proved that miRNAs may have clinical relevance as bio-pathologic markers for HCC classification, prognostic stratification, early diagnosis or follow-up of patients. Additionally, the demonstration that miRNAs themselves or anti-miRNA oligonucleotides could be successfully used for in vivo modulation of miRNA actions has shown significant potentials in molecularly targeted therapy. In this context, the liver represents an organ of election to test therapeutic possibilities associated with miRNAs.
引用
收藏
页码:500 / 521
页数:22
相关论文
共 352 条
[1]   let-7 microRNA functions as a potential growth suppressor in human colon cancer cells [J].
Akao, Yukihiro ;
Nakagawa, Yoshihito ;
Naoe, Tomoki .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2006, 29 (05) :903-906
[2]  
[Anonymous], CLIN CANC RES
[3]   Wnt/β-catenin signaling mediates oval cell response in rodents [J].
Apte, Udayan ;
Thompson, Michael D. ;
Cui, Shanshan ;
Liu, Bowen ;
Cieply, Benjamin ;
Monga, Satdarshan P. S. .
HEPATOLOGY, 2008, 47 (01) :288-295
[4]   MicroRNA-21 (miR-21) post-transcriptionally downregulates tumor suppressor Pdcd4 and stimulates invasion, intravasation and metastasis in colorectal cancer [J].
Asangani, I. A. ;
Rasheed, S. A. K. ;
Nikolova, D. A. ;
Leupold, J. H. ;
Colburn, N. H. ;
Post, S. ;
Allgayer, H. .
ONCOGENE, 2008, 27 (15) :2128-2136
[5]   Inhibitors of apoptosis proteins (IAPs) expression and their prognostic significance in hepatocellular carcinoma [J].
Augello, Claudia ;
Caruso, Luca ;
Maggioni, Marco ;
Donadon, Matteo ;
Montorsi, Marco ;
Santambrogio, Roberto ;
Torzilli, Guido ;
Vaira, Valentina ;
Pellegrini, Caterina ;
Roncalli, Massimo ;
Coggi, Guido ;
Bosari, Silvano .
BMC CANCER, 2009, 9
[6]   MicroRNA-122 Inhibits Tumorigenic Properties of Hepatocellular Carcinoma Cells and Sensitizes These Cells to Sorafenib [J].
Bai, Shoumei ;
Nasser, Mohd W. ;
Wang, Bo ;
Hsu, Shu-Hao ;
Datta, Jharna ;
Kutay, Huban ;
Yadav, Arti ;
Nuovo, Gerard ;
Kumar, Pawan ;
Ghoshal, Kalpana .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (46) :32015-32027
[7]   NATURAL-HISTORY OF SMALL UNTREATED HEPATOCELLULAR-CARCINOMA IN CIRRHOSIS - A MULTIVARIATE-ANALYSIS OF PROGNOSTIC FACTORS OF TUMOR-GROWTH RATE AND PATIENT SURVIVAL [J].
BARBARA, L ;
BENZI, G ;
GAIANI, S ;
FUSCONI, F ;
ZIRONI, G ;
SIRINGO, S ;
RIGAMONTI, A ;
BARBARA, C ;
GRIGIONI, W ;
MAZZIOTTI, A ;
BOLONDI, L .
HEPATOLOGY, 1992, 16 (01) :132-137
[8]   Downregulation of proapoptotic proteins Bax and Bcl-Xs in p53 overexpressing hepatocellular carcinomas [J].
Beerheide, W ;
Tan, YJ ;
Teng, E ;
Ting, AE ;
Jedpiyawongse, A ;
Srivatanakul, P .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 273 (01) :54-61
[9]   The MET receptor tyrosine kinase in invasion and metastasis [J].
Benvenuti, Silvia ;
Comoglio, Paolo M. .
JOURNAL OF CELLULAR PHYSIOLOGY, 2007, 213 (02) :316-325
[10]   Met, metastasis, motility and more [J].
Birchmeier, C ;
Birchmeier, W ;
Gherardi, E ;
Vande Woude, GF .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (12) :915-925