| Literature DB >> 33414893 |
Xia Chen1,2,3, Ai-Li Wang1,2,3, Yuan-Yuan Liu1,2,3, Chen-Xi Zhao1,2,3, Xue Zhou1,2,3, Hai-Long Liu1,2,3, Mo-Bin Lin1,2,3.
Abstract
Colorectal cancer (CRC) is a leading cause of cancer-related death around the world whose recurrence and metastasis rate is high. Due to the underlying unclear pathogenesis, it is hard so far to predict the tumorigenesis and prevent its recurrence. YAP/TAZ has been reported to be activated and functioned as a potential oncogene in multiple cancer types and proved to be essential for the carcinogenesis of most solid tumors. In the present study, we found that YAP/TAZ was markedly upregulated in CRC tissues comparing with the adjacent noncancerous tissues due to the downregulation of LATS2, the main upstream regulator. We further identified miR-429 as a direct regulator of LATS2-YAP/TAZ activation, suggesting that the miR-429-LATS2-YAP/TAZ might be novel effective diagnostic axis and therapeutic targets for CRC.Entities:
Year: 2020 PMID: 33414893 PMCID: PMC7769676 DOI: 10.1155/2020/5316276
Source DB: PubMed Journal: Oxid Med Cell Longev ISSN: 1942-0994 Impact factor: 6.543