期刊文献+

Hippo-YAP信号通路为靶点的肿瘤治疗研究进展 被引量:7

Research progress on cancer treatment targeting the Hippo-YAP signaling pathway
下载PDF
导出
摘要 Hippo通路是一个可调控细胞增殖和凋亡的信号转导通路,YAP(Yes-associated protein)为其主要效应分子。YAP为一个候选致癌因子,Hippo-YAP通路的异常与多种肿瘤的发生、发展密切相关。因此,以Hippo-YAP通路为靶点的治疗策略可能为肿瘤治疗提供新思路。一些可调控Hippo-YAP通路活性的药物/化合物如维替泊芬,可抑制肿瘤的发生或生长。本文主要对Hippo-YAP信号通路为靶点的肿瘤治疗研究进展进行综述。 Hippo pathway is a signaling network involved in the regulation of cell proliferation and apoptosis, whereas Yes-asso-ciated protein (YAP) is the major effector of the pathway. YAP is a candidate oncogene, and dysregulation of the Hippo-YAP pathway is closely related to the occurrence and progression of various tumors. Therefore, Hippo-YAP may provide a novel therapeutic target for cancer treatment. Some drugs or compounds that regulate the Hippo-YAP pathway activity, such as verteporfin, can inhibit the occurrence or growth of tumors. This review mainly focuses on the progress of studies on the use of Hippo-YAP signaling pathway as a target of cancer treatment strategies.
作者 宋娟 叶小群
出处 《中国肿瘤临床》 CAS CSCD 北大核心 2015年第17期876-880,共5页 Chinese Journal of Clinical Oncology
基金 国家自然科学基金项目(编号:81160277) 江西省教育厅科学技术研究重点项目(编号:GJJ14003)资助~~
关键词 Hippo通路 YAP 肿瘤 G蛋白偶联受体 维替泊芬 二甲双胍 Hippo pathway YAP tumor G protein coupled receptors verteporfin metformin
  • 相关文献

参考文献40

  • 1Johnson R, Halder G. The two faces of Hippo: targeting the Hip- po pathway for regenerative medicine and cancer treatment[J]. Nat Rev Drug Discov, 2014, 13(1):63-79.
  • 2Chart EH, Nousiainen M, Chalamalasetty RB, et al. The Ste20- like kinase Mst2 activates the human large tumor suppressor ki- nase Latsl[J]. Oncogene, 2005, 24(12):2076-2086.
  • 3Praskova M, Xia F, AvruchJ. MOBKLIA/MOBKL1B phosphor- ylation by MST1 and MST2 inhibits cell proliferation[J]. Curr Biol, 2008, 18(5):311-321.
  • 4Zhao B, Wei X, Li W, et al. Inactivation of YAP oncoprotein by the Hippo pathway is involved in cell contact inhibition and tis- sue growth control[J]. Genes Dev, 2007, 21(21):2747-2761.
  • 5Zhao B, Li L, Tumaneng K, et al. A coordinated phosphorylation by Lats and CK1 regulates YAP stability through SCF(beta- TRCP)[J]. Genes Dev, 2010, 24(1):72-85.
  • 6Sudol M, Shields DC, Farooq A. Structures of YAP protein do- mains reveal promising targets for development of new cancer drugs[J]. Semin Cell Dev Biol, 2012, 23 (7):827-833.
  • 7Tian W, YuJ, Tomchick DR, et al. Structural and functional anal- ysis of the YAP-binding domain of human TEAD2[J]. Proc Natl Acad Sci U S A, 2010, 107(16):7293-7298.
  • 8HanJC, Erdmann D, Mesrouze Y, et al. The TEAD4-YAP/TAZ protein-protein interaction: expected similarities and unexpected differences[J]. Chembiochem, 2013, 14(10):1218-1225.
  • 9Zhao B, Ye X, YuJ, et al. TEAD mediates YAP-dependent gene induction and growth control[J]. Genes Dev, 2008, 22(14):1962- 1971.
  • 10Li W, Cooper J, Zhou L, et al. Merlin/NF2 loss-driven tumori- genesis linked to CRE(DCAF1)-mediated inhibition of the hip- po pathway kinases Latsl and 2 in the nucleus[J]. Cancer Cell, 2014, 26(1):48-60.

同被引文献65

引证文献7

二级引证文献20

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部