| Literature DB >> 35017116 |
Xingwen Wang1, Shanliang Zheng1, Fan Yang1, Wenxin Zhang1, Dong Zhao1, Xuting Xue1, Qingyu Lin1, Yunfei He2, Guohong Hu2, Ying Hu3.
Abstract
Endocytosis of cell surface receptors is essential for cell migration and cancer metastasis. Rab5, a small GTPase of the Rab family, is a key regulator of endosome dynamics and thus cell migration. However, how its activity is regulated still remains to be addressed. Here, we identified a Rab5 inhibitor, a long non-coding RNA, namely HITT (HIF-1α inhibitor at translation level). Our data show that HITT expression is inversely associated with advanced stages and poor prognosis of lung adenocarcinoma patients with area under receiver operating characteristics (ROC) curve (AUC) 0.6473. Further study reveals that both endogenous and exogenous HITT inhibits single-cell migration by repressing β1 integrin endocytosis in lung adenocarcinoma. Mechanistically, HITT is physically associated with Rab5 at switch I via 1248-1347 nt and suppresses β1 integrin endocytosis and subsequent cancer metastasis by interfering with guanine nucleotide exchange factors (GEFs) for Rab5 binding. Collectively, these findings suggest that HITT directly participates in the regulation of Rab5 activity, leading to a decreased integrin internalization and cancer metastasis, which provides important insights into a mechanistic understanding of endocytosis and cancer metastasis.Entities:
Keywords: HITT; Rab5; cancer metastasis; endocytosis; β1-integrin
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Year: 2022 PMID: 35017116 PMCID: PMC8899701 DOI: 10.1016/j.ymthe.2022.01.014
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454