Insights into recent findings and clinical application of YAP and TAZ in cancer

被引:115
作者
Franklin, J. Matthew [1 ,2 ]
Wu, Zhengming [1 ,2 ]
Guan, Kun-Liang [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92103 USA
[2] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92103 USA
关键词
HIPPO SIGNALING PATHWAY; BREAST-CANCER; CELL-PROLIFERATION; TUMOR-GROWTH; YAP/TAZ; TEAD; WNT; TRANSCRIPTION; COACTIVATOR; PHOSPHORYLATION;
D O I
10.1038/s41568-023-00579-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The activities of YAP and TAZ have long been associated with cancer progression. In this Review, Franklin et al. provide an integrated perspective on the latest understandings of YAP and TAZ activation, including their role as a tumour suppressor, as well as advances in YAP and TAZ therapeutic treatments. Decades of research have mapped out the basic mechanics of the Hippo pathway. The paralogues Yes-associated protein (YAP) and transcriptional co-activator with PDZ-binding motif (TAZ), as the central transcription control module of the Hippo pathway, have long been implicated in the progression of various human cancers. The current literature regarding oncogenic YAP and TAZ activities consists mostly of context-specific mechanisms and treatments of human cancers. Furthermore, a growing number of studies demonstrate tumour-suppressor functions of YAP and TAZ. In this Review we aim to synthesize an integrated perspective of the many disparate findings regarding YAP and TAZ in cancer. We then conclude with the various strategies for targeting and treating YAP- and TAZ-dependent cancers.
引用
收藏
页码:512 / 525
页数:14
相关论文
共 187 条
[1]   Role of TAZ as Mediator of Wnt Signaling [J].
Azzolin, Luca ;
Zanconato, Francesca ;
Bresolin, Silvia ;
Forcato, Mattia ;
Basso, Giuseppe ;
Bicciato, Silvio ;
Cordenonsi, Michelangelo ;
Piccolo, Stefano .
CELL, 2012, 151 (07) :1443-1456
[2]   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-+
[3]   TAZ is required for metastatic activity and chemoresistance of breast cancer stem cells [J].
Bartucci, M. ;
Dattilo, R. ;
Moriconi, C. ;
Pagliuca, A. ;
Mottolese, M. ;
Federici, G. ;
Di Benedetto, A. ;
Todaro, M. ;
Stassi, G. ;
Sperati, F. ;
Amabile, M. I. ;
Pilozzi, E. ;
Patrizii, M. ;
Biffoni, M. ;
Maugeri-Sacca, M. ;
Piccolo, S. ;
De Maria, R. .
ONCOGENE, 2015, 34 (06) :681-690
[4]   The transcriptional coactivator TAZ regulates mesenchymal differentiation in malignant glioma [J].
Bhat, Krishna P. L. ;
Salazar, Katrina L. ;
Balasubramaniyan, Veerakumar ;
Wani, Khalida ;
Heathcock, Lindsey ;
Hollingsworth, Faith ;
James, Johanna D. ;
Gumin, Joy ;
Diefes, Kristin L. ;
Kim, Se Hoon ;
Turski, Alice ;
Azodi, Yasaman ;
Yang, Yuhui ;
Doucette, Tiffany ;
Colman, Howard ;
Sulman, Erik P. ;
Lang, Frederick F. ;
Rao, Ganesh ;
Copray, Sjef ;
Vaillant, Brian D. ;
Aldape, Kenneth D. .
GENES & DEVELOPMENT, 2011, 25 (24) :2594-2609
[5]   Role of Hippo Pathway-YAP/TAZ Signaling in Angiogenesis [J].
Boopathy, Gandhi T. K. ;
Hong, Wanjin .
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2019, 7
[6]   Small-Molecule Covalent Modification of Conserved Cysteine Leads to Allosteric Inhibition of the TEAD•Yap Protein-Protein Interaction [J].
Bum-Erdene, Khuchtumur ;
Zhou, Donghui ;
Gonzalez-Gutierrez, Giovanni ;
Ghozayel, Mona K. ;
Si, Yubing ;
Xu, David ;
Shannon, Harlan E. ;
Bailey, Barbara J. ;
Corson, Timothy W. ;
Pollok, Karen E. ;
Wells, Clark D. ;
Meroueh, Samy O. .
CELL CHEMICAL BIOLOGY, 2019, 26 (03) :378-+
[7]   Deletion of Lats1/2 in adult kidney epithelia leads to renal cell carcinoma [J].
Carter, Phoebe ;
Schnell, Ulrike ;
Chaney, Christopher ;
Tong, Betty ;
Pan, Xinchao ;
Ye, Jianhua ;
Mernaugh, Glenda ;
Cotton, Jennifer L. ;
Margulis, Vitaly ;
Mao, Junhao ;
Zent, Roy ;
Evers, Bret M. ;
Kapur, Payal ;
Carroll, Thomas J. .
JOURNAL OF CLINICAL INVESTIGATION, 2021, 131 (11)
[8]   Co-activation of STAT3 and YES-Associated Protein 1 (YAP1) Pathway in EGFR-Mutant NSCLC [J].
Chaib, Imane ;
Karachaliou, Niki ;
Pilotto, Sara ;
Codony Servat, Jordi ;
Cai, Xueting ;
Li, Xuefei ;
Drozdowskyj, Ana ;
Codony Servat, Carles ;
Yang, Jie ;
Hu, Chunping ;
Felipe Cardona, Andres ;
Vivanco, Guillermo Lopez ;
Vergnenegre, Alain ;
Miguel Sanchez, Jose ;
Provencio, Mariano ;
de Marinis, Filippo ;
Passaro, Antonio ;
Carcereny, Enric ;
Reguart, Noemi ;
Garcia Campelo, Charo ;
Teixido, Cristina ;
Sperduti, Isabella ;
Rodriguez, Sonia ;
Lazzari, Chiara ;
Verlicchi, Alberto ;
de Aguirre, Itziar ;
Queralt, Cristina ;
Wei, Jia ;
Estrada, Roger ;
Puig de la Bellacasa, Raimon ;
Luis Ramirez, Jose ;
Jacobsen, Kirstine ;
Ditzel, Henrik J. ;
Santarpia, Mariacarmela ;
Viteri, Santiago ;
Angel Molina, Miguel ;
Zhou, Caicun ;
Cao, Peng ;
Ma, Patrick C. ;
Bivona, Trever G. ;
Rosell, Rafael .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2017, 109 (09)
[9]  
Chan P, 2016, NAT CHEM BIOL, V12, P282, DOI [10.1038/NCHEMBIO.2036, 10.1038/nchembio.2036]
[10]   Coexistent ARID1A-PIK3CA mutations promote ovarian clear-cell tumorigenesis through pro-tumorigenic inflammatory cytokine signalling [J].
Chandler, Ronald L. ;
Damrauer, Jeffrey S. ;
Raab, Jesse R. ;
Schisler, Jonathan C. ;
Wilkerson, Matthew D. ;
Didion, John P. ;
Starmer, Joshua ;
Serber, Daniel ;
Yee, Della ;
Xiong, Jessie ;
Darr, David B. ;
de Villena, Fernando Pardo-Manuel ;
Kim, William Y. ;
Magnuson, Terry .
NATURE COMMUNICATIONS, 2015, 6