| Literature DB >> 33931764 |
Yuan-Ming He1,2, Xiu-Min Zhou3, Shuo-Yi Jiang1,2, Zu-Bin Zhang2, Bi-Yin Cao2, Jin-Bao Liu1, Yuan-Ying Zeng4, Jun Zhao5,6, Xin-Liang Mao7.
Abstract
The PTEN/AKT/mTOR signaling pathway is frequently dysregulated in non-small cell lung cancer (NSCLC), but the mechanisms are not well-understood. The present study found that the ubiquitin ligase TRIM25 is highly expressed in NSCLC tissues and promotes NSCLC cell survival and tumor growth. Mechanistic studies revealed that TRIM25 binds to PTEN and mediates its K63-linked ubiquitination at K266. This modification prevents the plasma membrane translocation of PTEN and reduces its phosphatase activity therefore accumulating PI(3,4,5)P3. TRIM25 thus activates the AKT/mTOR signaling. Moreover, we found that the antibacterial nitroxoline can activate PTEN by reducing its K63-linked polyubiquitination and sensitizes NSCLC to cisplatin-induced apoptosis. This study thus identified a novel modulation on the PTEN signaling pathway by TRIM25 and provides a potential target for NSCLC treatment.Entities:
Keywords: K63-linked polyubiquitination; PTEN; TRIM25; non-small cell lung cancer
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Year: 2021 PMID: 33931764 PMCID: PMC8888698 DOI: 10.1038/s41401-021-00662-z
Source DB: PubMed Journal: Acta Pharmacol Sin ISSN: 1671-4083 Impact factor: 6.150