School of Life Science and Technology, Harbin Institute of Technology, Harbin, Heilongjiang Province 150001, China.
Shanghai Institute of Nutrition and Health, University of Chinese Academy of Science, 320 Yuyang Road, Shanghai 200031, China.
Mol Ther. 2022 Mar 2;30(3):1071-1088. doi: 10.1016/j.ymthe.2022.01.014. Epub 2022 Jan 8.
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.
细胞表面受体的内吞对于细胞迁移和癌症转移是至关重要的。Rab5 是 Rab 家族的小 GTPase,是内体动力学和细胞迁移的关键调节因子。然而,其活性如何被调节仍有待解决。在这里,我们鉴定了一种 Rab5 抑制剂,一种长非编码 RNA,即 HITT(翻译水平的 HIF-1α抑制剂)。我们的数据表明,HITT 的表达与肺腺癌患者的晚期和预后不良呈负相关,接受者操作特征 (ROC) 曲线下面积 (AUC) 为 0.6473。进一步的研究表明,内源性和外源性的 HITT 通过抑制肺腺癌细胞中β1 整合素的内吞作用来抑制单细胞迁移。在机制上,HITT 通过 1248-1347nt 与开关 I 处的 Rab5 物理结合,并通过干扰 Rab5 结合的鸟嘌呤核苷酸交换因子 (GEFs) 来抑制β1 整合素内吞作用和随后的癌症转移。总之,这些发现表明 HITT 直接参与 Rab5 活性的调节,导致整合素内化减少和癌症转移,这为内吞作用和癌症转移的机制理解提供了重要的见解。