AMOTL1 enhances YAP1 stability and promotes YAP1-driven gastric oncogenesis
Publication in refereed journal

替代計量分析
.

其它資訊
摘要Hippo signaling functions to limit cellular growth, but the aberrant nuclear accumulation of its downstream YAP1 leads to carcinogenesis. YAP1/TEAD complex activates the oncogenic downstream transcription, such as CTGF and c-Myc. How YAP1 is protected in the cytoplasm from ubiquitin-mediated degradation remains elusive. In this study, a member of Angiomotin (Motin) family, AMOTL1 (Angiomotin Like 1), was screened out as the only one to promote YAP1 nuclear accumulation by several clinical cohorts, which was further confirmed by the cellular functional assays. The interaction between YAP1 and AMOTL1 was suggested by co-immunoprecipitation and immunofluorescent staining. The clinical significance of the AMOTL1-YAP1-CTGF axis in gastric cancer (GC) was analyzed by multiple clinical cohorts. Moreover, the therapeutic effect of targeting the oncogenic axis was appraised by drug-sensitivity tests and xenograft-formation assays. The upregulation of AMOTL1 is associated with unfavorable clinical outcomes of GC, and knocking down AMOTL1 impairs its oncogenic properties. The cytoplasmic interaction between AMOTL1 and YAP1 protects each other from ubiquitin-mediated degradation. AMOTL1 promotes YAP1 translocation into the nuclei to activate the downstream expression, such as CTGF. Knocking down AMOTL1, YAP1, and CTGF enhances the therapeutic efficacies of the first-line anticancer drugs. Taken together, AMOTL1 plays an oncogenic role in gastric carcinogenesis through interacting with YAP1 and promoting its nuclear accumulation. A combination of AMOTL1, YAP1, and CTGF expression might serve as a surrogate of Hippo activation status. The co-activation of the AMOTL1/YAP1-CTGF axis is associated with poor clinical outcomes of GC patients, and targeting this oncogenic axis may enhance the chemotherapeutic effects.
著者Yuhang ZHOU, Jinglin ZHANG, Hui LI, Tingting HUANG, Chi Chun WONG, Feng WU, Man WU, Nuoqing WENG, Liping LIU, Alfred S. L. CHENG, Jun YU, Nathalie WONG, Kwok Wai LO, Patrick M. K. TANG, Wei KANG, Ka Fai TO
期刊名稱Oncogene,Oncogene
出版年份2020
月份5
卷號39
期次22
出版社Nature Publishing Group
頁次4375 - 4389
國際標準期刊號0950-9232
電子國際標準期刊號1476-5594
語言英式英語

上次更新時間 2020-23-11 於 23:44