The Hippo-YAP pathway: new connections between regulation of organ size and cancer

被引:392
作者
Zhao, Bin [2 ,3 ,4 ]
Lei, Qun-Ying [1 ,5 ]
Guan, Kun-Liang [2 ,3 ]
机构
[1] Fudan Univ, Dept Biol Chem, Sch Med, Shanghai 200032, Peoples R China
[2] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
[4] Univ Michigan, Dept Biol Chem, Ann Arbor, MI 48109 USA
[5] Fudan Univ, Mol & Cellular Biol Lab, Inst Biomed Sci, Shanghai 200032, Peoples R China
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
D O I
10.1016/j.ceb.2008.10.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The control of organ size is a basic biological question. In the past several years, the Hippo signaling pathway has been delineated and shown to be crucial in control of organ size in both Drosophila and mammals. Acting downstream of the Hippo pathway is the Yki/YAP/TAZ transcription co-activators. In mammalian cells, the Hippo pathway kinase cascade inhibits YAP and its paralog TAZ by phosphorylation and promotion of their cytoplasmic localization. The TEAD family transcription factors have recently been identified as evolutionarily conserved key mediators of YAP biological functions. yap is a candidate oncogene, and several other components of the Hippo pathway are tumor suppressors. Dysregulation of the Hippo pathway contributes to the loss of contact inhibition observed in cancer cells. Therefore, the Hippo-YAP pathway connects the regulation of organ size and tumorigenesis.
引用
收藏
页码:638 / 646
页数:9
相关论文
共 77 条
[1]   Akt phosphorylates the Yes-associated protein, YAP, to induce interaction with 14-3-3 and attenuation of p73-mediated apoptosis [J].
Basu, S ;
Totty, NF ;
Irwin, MS ;
Sudol, M ;
Downward, J .
MOLECULAR CELL, 2003, 11 (01) :11-23
[2]   Fat cadherin modulates organ size in Drosophila via the Salvador/Warts/Hippo signaling pathway [J].
Bennett, F. Christian ;
Harvey, Kieran F. .
CURRENT BIOLOGY, 2006, 16 (21) :2101-2110
[3]   How size is controlled: from Hippos to Yorkies [J].
Buttitta, Laura A. ;
Edgar, Bruce A. .
NATURE CELL BIOLOGY, 2007, 9 (11) :1225-1227
[4]   Association of mammalian sterile twenty kinases, Mst1 and Mst2, with hSalvador via C-terminal coiled-coil domains, leads to its stabilization and phosphorylation [J].
Callus, Bernard A. ;
Verhagen, Anne M. ;
Vaux, David L. .
FEBS JOURNAL, 2006, 273 (18) :4264-4276
[5]   YAP1 increases organ size and expands undifferentiated progenitor cells [J].
Camargo, Fernando D. ;
Gokhale, Sumita ;
Johnnidis, Jonathan B. ;
Fu, Dongdong ;
Bell, George W. ;
Jaenisch, Rudolf ;
Brummelkamp, Thijn R. .
CURRENT BIOLOGY, 2007, 17 (23) :2054-2060
[6]   THE SCALLOPED GENE ENCODES A NOVEL, EVOLUTIONARILY CONSERVED TRANSCRIPTION FACTOR REQUIRED FOR SENSORY ORGAN DIFFERENTIATION IN DROSOPHILA [J].
CAMPBELL, S ;
INAMDAR, M ;
RODRIGUES, V ;
RAGHAVAN, V ;
PALAZZOLO, M ;
CHOVNICK, A .
GENES & DEVELOPMENT, 1992, 6 (03) :367-379
[7]   The Ste20-like kinase Mst2 activates the human large tumor suppressor kinase Lats1 [J].
Chan, EH ;
Nousiainen, M ;
Chalamalasetty, RB ;
Schafër, A ;
Nigg, EA ;
Silljé, HHW .
ONCOGENE, 2005, 24 (12) :2076-2086
[8]   A role for TAZ in migration, invasion, and tumorigenesis of breast cancer cells [J].
Chan, Siew Wee ;
Lim, Chun Jye ;
Guo, Ke ;
Ng, Chee Peng ;
Lee, Ian ;
Hunziker, Walter ;
Zeng, Qi ;
Hong, Wanjin .
CANCER RESEARCH, 2008, 68 (08) :2592-2598
[9]   Delineation of a Fat tumor suppressor pathway [J].
Cho, Eunjoo ;
Feng, Yongqiang ;
Rauskolb, Cordelia ;
Maitra, Sushmita ;
Fehon, Rick ;
Irvine, Kenneth D. .
NATURE GENETICS, 2006, 38 (10) :1142-1150
[10]   Elucidation of a universal size-control mechanism in Drosophila and mammals [J].
Dong, Jixin ;
Feldmann, Georg ;
Huang, Jianbin ;
Wu, Shian ;
Zhang, Nailing ;
Comerford, Sarah A. ;
Gayyed, Mariana F. ;
Anders, Robert A. ;
Maitra, Anirban ;
Pan, Duojia .
CELL, 2007, 130 (06) :1120-1133