Brg-1 targeting of novel miR550a-5p/RNF43/Wnt signaling axis regulates colorectal cancer metastasis

被引:55
作者
Wang, G. [1 ]
Fu, Y. [1 ]
Yang, X. [1 ]
Luo, X. [1 ]
Wang, J. [2 ]
Gong, J. [3 ]
Hu, J. [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Canc Res Inst, 1095 Jiefang Rd, Wuhan 430030, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Dept Immunol, 1095 Jiefang Rd, Wuhan 430030, Peoples R China
[3] Huazhong Univ Sci & Technol, Tongji Hosp, Mol Med Ctr, 1095 Jiefang Rd, Wuhan 430030, Peoples R China
关键词
NUCLEOSOME-REMODELING COMPLEXES; SWI/SNF COMPLEX; HEPATOCELLULAR-CARCINOMA; UBIQUITIN LIGASE; CELL; RNF43; EXPRESSION; MUTATIONS; COMPONENT; FAMILY;
D O I
10.1038/onc.2015.124
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Metastasis is one of the main causes of death in patients with colorectal cancer (CRC). Brg-1 is a central component of the SWItch/Sucrose NonFermentable chromatin-remodeling complex, which features a bromodomain and helicase/ATPase activity. The gene encoding Brg-1 is frequently mutated or silenced in human cancers. Several reports have proposed Brg-1 as a tumor suppressor; however, little is known about its role in oncogenesis and metastasis. Here we demonstrated that decreased Brg-1 regulates a novel miR-550a-5p/RNF43/Wnt/beta-catenin signaling pathway, to promote CRC metastasis in vitro and in vivo. In particular, we used high-throughput RNA-sequencing analysis to show that Brg-1 negatively regulates miR-550a-5p in CRC cells. We further found that Brg-1 inhibits the transcriptional activity of miR-550a-5p promoter, and that decreased Brg-1 expression increased miR-550a-5p expression. We also identified ring finger 43 (RNF43), an inhibitor of Wnt/beta-catenin signaling, as a target of miR-550a-5p. Knockdown of Brg-1 by small interfering RNA led to decreased RNF43 expression, increased Wnt signaling and increased CRC cell migration and invasion. This novel pathway defines a new function for Brg-1 and provides potential targets for the treatment of Brg-1 mutant and loss-of-function tumors.
引用
收藏
页码:651 / 661
页数:11
相关论文
共 45 条
[1]   Oncogenic β-catenin triggers an inflammatory response that determines the aggressiveness of hepatocellular carcinoma in mice [J].
Anson, Marie ;
Crain-Denoyelle, Anne-Marie ;
Baud, Veronique ;
Chereau, Fanny ;
Gougelet, Angelique ;
Terris, Benoit ;
Yamagoe, Satoshi ;
Colnot, Sabine ;
Viguier, Mireille ;
Perret, Christine ;
Couty, Jean-Pierre .
JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (02) :586-599
[2]   BRG1 Is a Prognostic Marker and Potential Therapeutic Target in Human Breast Cancer [J].
Bai, Jin ;
Mei, Pengjin ;
Zhang, Cuipeng ;
Chen, Feifei ;
Li, Chen ;
Pan, Zhenqiang ;
Liu, Hui ;
Zheng, Junnian .
PLOS ONE, 2013, 8 (03)
[3]   Characterization of mammary tumors from Brg1 heterozygous mice [J].
Bultman, S. J. ;
Herschkowitz, J. I. ;
Godfrey, V. ;
Gebuhr, T. C. ;
Yaniv, M. ;
Perou, C. M. ;
Magnuson, T. .
ONCOGENE, 2008, 27 (04) :460-468
[4]   The colorectal microRNAome [J].
Cummins, JM ;
He, YP ;
Leary, RJ ;
Pagliarini, R ;
Diaz, LA ;
Sjoblom, T ;
Barad, O ;
Bentwich, Z ;
Szafranska, AE ;
Labourier, E ;
Raymond, CK ;
Roberts, BS ;
Juhl, H ;
Kinzler, KW ;
Vogelstein, B ;
Velculescu, VE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (10) :3687-3692
[5]   Prohibitin and the SWI/SNF ATPase subunit BRG1 are required for effective androgen antagonist-mediated transcriptional repression of androgen receptor-regulated genes [J].
Dai, Yan ;
Ngo, Duyen ;
Jacob, Johanna ;
Forman, Lora W. ;
Faller, Douglas V. .
CARCINOGENESIS, 2008, 29 (09) :1725-1733
[6]   Tumour-cell invasion and migration: Diversity and escape mechanisms [J].
Friedl, P ;
Wolf, K .
NATURE REVIEWS CANCER, 2003, 3 (05) :362-374
[7]   The chromatin-remodeling enzyme BRG1 plays an essential role in primitive erythropoiesis and vascular development [J].
Griffin, Courtney T. ;
Brennan, Jennifer ;
Magnuson, Terry .
DEVELOPMENT, 2008, 135 (03) :493-500
[8]   SRG3, a core component of mouse SWI/SNF complex, is essential for extra-embryonic vascular development [J].
Han, Daehee ;
Jeon, Shin ;
Sohn, Dong Hyun ;
Lee, Changjin ;
Ahn, Sangil ;
Kim, Won Kyu ;
Chung, Heekyoung ;
Seong, Rho Hyun .
DEVELOPMENTAL BIOLOGY, 2008, 315 (01) :136-146
[9]   Inactivating mutations of RNF43 confer Wnt dependency in pancreatic ductal adenocarcinoma [J].
Jiang, Xiaomo ;
Hao, Huai-Xiang ;
Growney, Joseph D. ;
Woolfenden, Steve ;
Bottiglio, Cindy ;
Ng, Nicholas ;
Lu, Bo ;
Hsieh, Mindy H. ;
Bagdasarian, Linda ;
Meyer, Ronald ;
Smith, Timothy R. ;
Avello, Monika ;
Charlat, Olga ;
Xie, Yang ;
Porter, Jeffery A. ;
Pan, Shifeng ;
Liu, Jun ;
McLaughlin, Margaret E. ;
Cong, Feng .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (31) :12649-12654
[10]   Genetic profile of hepatocellular carcinoma revealed by array-based comparative genomic hybridization: Identification of genetic indicators to predict patient outcome [J].
Katoh, H ;
Shibata, T ;
Kokubu, A ;
Ojima, H ;
Loukopoulos, P ;
Kanai, Y ;
Kosuge, T ;
Fukayama, M ;
Kondo, T ;
Sakamoto, M ;
Hosoda, F ;
Ohki, M ;
Imoto, I ;
Inazawa, J ;
Hirohashi, S .
JOURNAL OF HEPATOLOGY, 2005, 43 (05) :863-874