| Literature DB >> 33553178 |
Yue Liu1,2,3,4, Wenjuan Zhang2, Shiwen Wang1,2,3,4, Lili Cai2, Yanyu Jiang2, Yongfu Pan2, Yupei Liang2, Jingrong Xian1,2,3,4, Lijun Jia2, Lihui Li2, Hu Zhao1,3,4, Yanmei Zhang1,3,4.
Abstract
Rho family GTPase RhoB is the critical signaling component controlling the inflammatory response elicited by pro-inflammatory cytokines. However, the underlying mechanisms of RhoB degradation in inflammatory response remain unclear. In this study, for the first time, we identified that TNFAIP1, an adaptor protein of Cullin3 E3 ubiquitin ligases, coordinated with Cullin3 to mediate RhoB degradation through ubiquitin proteasome system. In addition, we demonstrated that downregulation of TNFAIP1 induced the expression of pro-inflammatory cytokines IL-6 and IL-8 in TNFα-stimulated hepatocellular carcinoma cells through the activation of p38/JNK MAPK pathway via blocking RhoB degradation. Our findings revealed a novel mechanism of RhoB degradation and provided a potential strategy for anti-inflammatory intervention of tumors by targeting TNFAIP1-RhoB axis.Entities:
Keywords: CRL3s; MAPK signaling; RhoB; TNFAIP1; inflammatory response
Year: 2021 PMID: 33553178 PMCID: PMC7859282 DOI: 10.3389/fcell.2021.617134
Source DB: PubMed Journal: Front Cell Dev Biol ISSN: 2296-634X