河马信号通路
癌变
磷酸化
细胞质
泛素
细胞生物学
癌细胞
细胞生长
化学
癌症研究
细胞
转移
信号转导
生物
癌症
生物化学
遗传学
基因
作者
Ilju Kim,Pattawika Lertpatipanpong,Yongdae Yoon,Jaehak Lee,Yukyung Hong,Kanokkan Boonruang,Junsun Ryu,Seung Joon Baek
标识
DOI:10.1016/j.bbamcr.2023.119556
摘要
Several diseases are associated with improper regulation of the Hippo pathway, which plays an important role in cell proliferation and cancer metastasis. Overactivation of the YAP and TAZ proteins accelerates cell proliferation, invasion, and migration during tumorigenesis. Tolfenamic acid (TA) is a non-steroidal anti-inflammatory drug (NSAID) that exhibits activity against various types of cancer. In this study, we observed that TA decreased YAP and TAZ protein levels in cancer cells. TA increased the phosphorylation of YAP and TAZ, leading to the degradation of YAP and TAZ in the cytoplasm and nucleus. TA predominantly affected multiple phosphodegron sites in the YAP and TAZ and lowered 14-3-3β protein expression, causing YAP and TAZ to enter the ubiquitination pathway. Proteins that affect YAP and TAZ regulation, such as NAG-1 and several YAP/TAZ E3 ligases, were not involved in TA-mediated YAP/TAZ degradation. In summary, our results indicate that TA affects phosphodegron sites on YAP/TAZ, demonstrating a novel effect of TA in tumorigenesis.
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