Targeting Wnt signaling in colorectal cancer. A Review in the Theme: Cell Signaling: Proteins, Pathways and Mechanisms

被引:262
作者
Novellasdemunt, Laura [1 ]
Antas, Pedro [1 ]
Li, Vivian S. W. [1 ]
机构
[1] Francis Crick Inst, Mill Hill Lab, London NW7 1AA, England
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2015年 / 309卷 / 08期
基金
英国医学研究理事会;
关键词
Wnt signaling pathway; colorectal cancer; adenomatous polyposis coli; beta-catenin; drug targeting; small molecules; SMALL-MOLECULE INHIBITOR; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; FAMILIAL ADENOMATOUS POLYPOSIS; WNT/BETA-CATENIN PATHWAY; COLON-CARCINOMA CELLS; WIDE RNAI SCREEN; BETA-CATENIN; MICROSATELLITE INSTABILITY; TUMOR-GROWTH; MONOCLONAL-ANTIBODY;
D O I
10.1152/ajpcell.00117.2015
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The evolutionarily conserved Wnt signaling pathway plays essential roles during embryonic development and tissue homeostasis. Notably, comprehensive genetic studies in Drosophila and mice in the past decades have demonstrated the crucial role of Wnt signaling in intestinal stem cell maintenance by regulating proliferation, differentiation, and cell-fate decisions. Wnt signaling has also been implicated in a variety of cancers and other diseases. Loss of the Wnt pathway negative regulator adenomatous polyposis coli (APC) is the hallmark of human colorectal cancers (CRC). Recent advances in high-throughput sequencing further reveal many novel recurrent Wnt pathway mutations in addition to the well-characterized APC and beta-catenin mutations in CRC. Despite attractive strategies to develop drugs for Wnt signaling, major hurdles in therapeutic intervention of the pathway persist. Here we discuss the Wnt-activating mechanisms in CRC and review the current advances and challenges in drug discovery.
引用
收藏
页码:C511 / C521
页数:11
相关论文
共 128 条
[1]   beta-catenin is a target for the ubiquitin-proteasome pathway [J].
Aberle, H ;
Bauer, A ;
Stappert, J ;
Kispert, A ;
Kemler, R .
EMBO JOURNAL, 1997, 16 (13) :3797-3804
[2]   Palmitoylation and ubiquitination regulate exit of the Wnt signaling protein LRP6 from the endoplasmic reticulum [J].
Abrami, Laurence ;
Kunz, Beatrice ;
Lacovache, Ioan ;
Van der Goot, F. Gisou .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (14) :5384-5389
[3]   Vitamin D-3 analog, EB1089, inhibits growth of subcutaneous xenografts of the human colon cancer cell line, LoVo, in a nude mouse model [J].
Akhter, J ;
Chen, XH ;
Bowrey, P ;
Bolton, EJ ;
Morris, DL .
DISEASES OF THE COLON & RECTUM, 1997, 40 (03) :317-321
[4]  
Avizienyte E, 1998, CANCER RES, V58, P2087
[5]   YAP/TAZ Incorporation in the β-Catenin Destruction Complex Orchestrates the Wnt Response [J].
Azzolin, Luca ;
Panciera, Tito ;
Soligo, Sandra ;
Enzo, Elena ;
Bicciato, Silvio ;
Dupont, Sirio ;
Bresolin, Silvia ;
Frasson, Chiara ;
Basso, Giuseppe ;
Guzzardo, Vincenza ;
Fassina, Ambrogio ;
Cordenonsi, Michelangelo ;
Piccolo, Stefano .
CELL, 2014, 158 (01) :157-170
[6]   Identification of stem cells in small intestine and colon by marker gene Lgr5 [J].
Barker, Nick ;
van Es, Johan H. ;
Kuipers, Jeroen ;
Kujala, Pekka ;
van den Born, Maaike ;
Cozijnsen, Miranda ;
Haegebarth, Andrea ;
Korving, Jeroen ;
Begthel, Harry ;
Peters, Peter J. ;
Clevers, Hans .
NATURE, 2007, 449 (7165) :1003-U1
[7]   A randomized trial of aspirin to prevent colorectal adenomas [J].
Baron, JA ;
Cole, BF ;
Sandler, RS ;
Haile, RW ;
Ahnen, D ;
Bresalier, R ;
McKeown-Eyssen, G ;
Summers, RW ;
Rothstein, R ;
Burke, CA ;
Snover, DC ;
Church, TR ;
Allen, JI ;
Beach, M ;
Beck, GJ ;
Bond, JH ;
Byers, T ;
Greenberg, ER ;
Mandel, JS ;
Marcon, N ;
Mott, LA ;
Pearson, L ;
Saibil, F ;
van Stolk, RU .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (10) :891-899
[8]   Restriction of intestinal stem cell expansion and the regenerative response by YAP [J].
Barry, Evan R. ;
Morikawa, Teppei ;
Butler, Brian L. ;
Shrestha, Kriti ;
de la Rosa, Rosemarie ;
Yan, Kelley S. ;
Fuchs, Charles S. ;
Magness, Scott T. ;
Smits, Ron ;
Ogino, Shuji ;
Kuo, Calvin J. ;
Camargo, Fernando D. .
NATURE, 2013, 493 (7430) :106-+
[9]   Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion [J].
Bass, Adam J. ;
Lawrence, Michael S. ;
Brace, Lear E. ;
Ramos, Alex H. ;
Drier, Yotam ;
Cibulskis, Kristian ;
Sougnez, Carrie ;
Voet, Douglas ;
Saksena, Gordon ;
Sivachenko, Andrey ;
Jing, Rui ;
Parkin, Melissa ;
Pugh, Trevor ;
Verhaak, Roel G. ;
Stransky, Nicolas ;
Boutin, Adam T. ;
Barretina, Jordi ;
Solit, David B. ;
Vakiani, Evi ;
Shao, Wenlin ;
Mishina, Yuji ;
Warmuth, Markus ;
Jimenez, Jose ;
Chiang, Derek Y. ;
Signoretti, Sabina ;
Kaelin, William G., Jr. ;
Spardy, Nicole ;
Hahn, William C. ;
Hoshida, Yujin ;
Ogino, Shuji ;
DePinho, Ronald A. ;
Chin, Lynda ;
Garraway, Levi A. ;
Fuchs, Charles S. ;
Baselga, Jose ;
Tabernero, Josep ;
Gabriel, Stacey ;
Lander, Eric S. ;
Getz, Gad ;
Meyerson, Matthew .
NATURE GENETICS, 2011, 43 (10) :964-U67
[10]   Functional interaction of beta-catenin with the transcription factor LEF-1 [J].
Behrens, J ;
vonKries, JP ;
Kuhl, M ;
Bruhn, L ;
Wedlich, D ;
Grosschedl, R ;
Birchmeier, W .
NATURE, 1996, 382 (6592) :638-642