新型长非编码 RNA LINC02820 增强 TNF 信号通路重塑细胞骨架并增强食管鳞状细胞癌的转移。

Novel long noncoding RNA LINC02820 augments TNF signaling pathway to remodel cytoskeleton and potentiate metastasis in esophageal squamous cell carcinoma.

机构信息

Department of Experimental Research, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, People's Republic of China.

Department of Nuclear Medicine, The Second People's Hospital of Shenzhen, Shenzhen, People's Republic of China.

出版信息

Cancer Gene Ther. 2023 Feb;30(2):375-387. doi: 10.1038/s41417-022-00554-2. Epub 2022 Nov 10.

Abstract

Esophageal squamous cell carcinoma (ESCC) is one of the most common malignant tumors in China. However, there are no targets to treat ESCC because the molecular mechanism behind the cancer is still unclear. Here, we found a novel long noncoding RNA LINC02820 was upregulated in ESCC and associated with the ESCC clinicopathological stage. Through a series of functional experiments, we observed that LINC02820 only promoted the migration and invasion capabilities of ESCC cell lines. Mechanically, we found that LINC02820 may affect the cytoskeletal remodeling, interact with splice factor 3B subunit 3 (SF3B3), and cooperate with TNFα to amplify the NF-κB signaling pathway, which can lead to ESCC metastasis. Overall, our findings revealed that LINC02820 is a potential biomarker and therapeutic target for the diagnosis and treatment of ESCC.

摘要

食管鳞状细胞癌(ESCC)是中国最常见的恶性肿瘤之一。然而,由于癌症背后的分子机制尚不清楚,因此尚无治疗 ESCC 的靶点。在这里,我们发现一种新型长非编码 RNA LINC02820 在 ESCC 中上调,并与 ESCC 的临床病理分期相关。通过一系列功能实验,我们观察到 LINC02820 仅促进 ESCC 细胞系的迁移和侵袭能力。从机制上讲,我们发现 LINC02820 可能会影响细胞骨架重塑,与剪接因子 3B 亚基 3(SF3B3)相互作用,并与 TNFα 合作放大 NF-κB 信号通路,从而导致 ESCC 转移。总体而言,我们的研究结果表明,LINC02820 是 ESCC 诊断和治疗的有潜力的生物标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2189/9935391/44ac07e2241b/41417_2022_554_Fig1_HTML.jpg

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