Up-regulation of dicer, a component of the microRNA machinery, in prostate adenocarcinoma

被引:388
作者
Chiosea, Simion
Jelezcova, Elena
Chandran, Uma
Acquafondata, Marie
McHale, Teresa
Sobol, Robert W.
Dhir, Rajiv
机构
[1] Univ Pittsburgh, Med Ctr, Dept Pathol, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Sch Med, Dept Pharmacol, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Inst Canc, Hillman Canc Ctr, Pittsburgh, PA USA
关键词
D O I
10.2353/ajpath.2006.060480
中图分类号
R36 [病理学];
学科分类号
100104 [病理学与病理生理学];
摘要
MicroRNAs are small noncoding; 18- to 24-nt RNAs that are predicted to regulate expression of as many as 30% of protein-encoding genes. in prostate adenocarcinoma, 39 microRNAs are up-regulated, and six microRNAs are down-regulated. Production and function of microRNA requires coordinated processing by proteins of the microRNA machinery. Dicer, an RNase M endonuclease, is an essential component of the microRNA machinery. From a gene array analysis of 16 normal prostate tissue samples, 64 organ-confined, and four metastatic prostate adenocarcinomas, we identified an up-regulation of major components of the microRNA machinery, including Dicer, in metastatic prostate adenocarcinoma. inummohistochemical studies on a tissue microarray consisting of 232 prostate specimens confirmed up-regulation of Dicer in prostatic intraepithelial neoplasia and in 81% of prostate adenocarcinoma. The increased Dicer level in prostate adenocarcinoma correlated with clinical stage, lymph node status, and Gleason score. Western blot analysis of benign and neoplastic prostate cell lines further confirmed Dicer up-regulation in prostate adenocarcinoma. Dicer up-regulation may explain an almost global increase of microRNA expression in prostate adenocarcinoma. The presence of up-regulated microRNA machinery may predict the susceptibility of prostate adenocarcinoma to RNA interference-based therapy.
引用
收藏
页码:1812 / 1820
页数:9
相关论文
共 52 条
[1]
Androgen responsive adult human prostatic epithelial cell lines immortalized by human papillomavirus 18 [J].
Bello, D ;
Webber, MM ;
Kleinman, HK ;
Wartinger, DD ;
Rhim, JS .
CARCINOGENESIS, 1997, 18 (06) :1215-1223
[2]
Phylogenetic shadowing and computational identification of human microRNA genes [J].
Berezikov, E ;
Guryev, V ;
van de Belt, J ;
Wienholds, E ;
Plasterk, RHA ;
Cuppen, E .
CELL, 2005, 120 (01) :21-24
[3]
Bonkhoff H, 1996, EUR UROL, V30, P201
[4]
Ago1 and Dcr1, two core components of the RNA interference pathway, functionally diverge from Rdp1 in regulating cell cycle events in Schizosaccharomyces pombe [J].
Carmichael, JB ;
Provost, P ;
Ekwall, K ;
Hobman, TC .
MOLECULAR BIOLOGY OF THE CELL, 2004, 15 (03) :1425-1435
[5]
Differences in gene expression in prostate cancer, normal appearing prostate tissue adjacent to cancer and prostate tissue from cancer free organ donors [J].
Chandran, UR ;
Dhir, R ;
Ma, CQ ;
Michalopoulos, G ;
Becich, M ;
Gilbertson, J .
BMC CANCER, 2005, 5 (1)
[6]
TRBP recruits the Dicer complex to Ago2 for microRNA processing and gene silencing [J].
Chendrimada, TP ;
Gregory, RI ;
Kumaraswamy, E ;
Norman, J ;
Cooch, N ;
Nishikura, K ;
Shiekhattar, R .
NATURE, 2005, 436 (7051) :740-744
[7]
miR-15 and miR-16 induce apoptosis by targeting BCL2 [J].
Cimmino, A ;
Calin, GA ;
Fabbri, M ;
Iorio, MV ;
Ferracin, M ;
Shimizu, M ;
Wojcik, SE ;
Aqeilan, RI ;
Zupo, S ;
Dono, M ;
Rassenti, L ;
Alder, H ;
Volinia, S ;
Liu, CG ;
Kipps, TJ ;
Negrini, M ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (39) :13944-13949
[8]
miRNAs, cancer, and stem cell division [J].
Croce, CM ;
Calin, GA .
CELL, 2005, 122 (01) :6-7
[9]
siRNAs can function as miRNAs [J].
Doench, JG ;
Petersen, CP ;
Sharp, PA .
GENES & DEVELOPMENT, 2003, 17 (04) :438-442
[10]
Post-transcriptional gene silencing by siRNAs and miRNAs [J].
Filipowicz, W ;
Jaskiewicz, L ;
Kolb, FA ;
Pillai, RS .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2005, 15 (03) :331-341