RNAi-mediated knockdown of target genes: a promising strategy for pancreatic cancer research

被引:21
作者
Chang, Hong
机构
[1] Shandong Univ, Shandong Provincial Hosp, Sch Med, Dept Surg, Shandong 250021, Peoples R China
[2] Shandong Univ, Sch Med, Shandong, Peoples R China
关键词
review; pancreatic cancer; RNA interference;
D O I
10.1038/sj.cgt.7701063
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Pancreatic cancer is one of the most aggressive malignancies with a very poor prognosis, partially due to its very low accessibility to resection and resistance to chemoradiotherapy. As such, it is reasonable to find more effective, specific therapies and the related therapeutic targets. The identification of certain genes contributing to the tumorigenesis and poor prognosis provides the specific targets for efficient silencing by RNA interference (RNAi). As a powerful tool to suppress gene expression in mammalian cells, RNAi can be directed against pancreatic cancer through various pathways, including the inhibition of overexpressed oncogenes, suppression of tumor growth, metastasis and enhancement of apoptosis. In combination with chemoradiotherapy agents, RNAi can also attenuate the chemoradiation resistance of pancreatic cancer. In addition, RNAi has been used to define the 'loss of function' of endogenous genes in pancreatic cancer. This review provides a brief introduction to recent developments of RNAi applications in pancreatic cancer studies and suggestions for further exploration. It substantially demonstrates that RNAi holds a promising therapeutic potential as a future treatment for pancreatic cancer.
引用
收藏
页码:677 / 685
页数:9
相关论文
共 95 条
[1]   Integrin-linked kinase expression increases with ovarian turnour grade and is sustained by peritoneal tumour fluid [J].
Ahmed, N ;
Riley, C ;
Oliva, K ;
Stutt, E ;
Rice, GE ;
Quinn, MA .
JOURNAL OF PATHOLOGY, 2003, 201 (02) :229-237
[2]   A role for survivin in radioresistance of pancreatic cancer cells [J].
Asanuma, K ;
Kobayashi, D ;
Furuya, D ;
Tsuji, N ;
Yagihashi, A ;
Watanabe, N .
JAPANESE JOURNAL OF CANCER RESEARCH, 2002, 93 (09) :1057-1062
[3]   Role for a bidentate ribonuclease in the initiation step of RNA interference [J].
Bernstein, E ;
Caudy, AA ;
Hammond, SM ;
Hannon, GJ .
NATURE, 2001, 409 (6818) :363-366
[4]   Comparison of antisense oligonucleotides and siRNAs in cell culture and in vivo [J].
Bertrand, JR ;
Pottier, M ;
Vekris, A ;
Opolon, P ;
Maksimenko, A ;
Malvy, C .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 296 (04) :1000-1004
[5]   Gene therapy developments for pancreatic cancer [J].
Bhattacharrya, M ;
Lemoine, NR .
BEST PRACTICE & RESEARCH CLINICAL GASTROENTEROLOGY, 2006, 20 (02) :285-298
[6]   Stable suppression of tumorigenicity by virus-mediated RNA interference [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
CANCER CELL, 2002, 2 (03) :243-247
[7]   Survivin-directed RNA interference cocktail is a potent suppressor of tumour growth in vivo [J].
Caldas, H ;
Holloway, MP ;
Hall, BM ;
Qualman, SJ ;
Altura, RA .
JOURNAL OF MEDICAL GENETICS, 2006, 43 (02) :119-128
[8]   Expression and localization of GLUT1 and GLUT12 in prostate carcinoma [J].
Chandler, JD ;
Williams, ED ;
Slavin, JL ;
Best, JD ;
Rogers, S .
CANCER, 2003, 97 (08) :2035-2042
[9]   Down-regulation of vascular endothelial cell growth factor-C expression using small interfering RNA vectors in mammary tumors inhibits tumor lymphangiogenesis and spontaneous metastasis and enhances survival [J].
Chen, ZT ;
Varney, ML ;
Backora, MW ;
Cowan, K ;
Solheim, JC ;
Talmadge, JE ;
Singh, RK .
CANCER RESEARCH, 2005, 65 (19) :9004-9011
[10]   Small RNAs make big splash [J].
Couzin, J .
SCIENCE, 2002, 298 (5602) :2296-2297