The E3 ubiquitin ligase TRIM31 enhances the progression of esophageal cancer through the ubiquitination of BBOX1.

IF 4.4 2区 生物学 Q2 CELL BIOLOGY
G E Lei, Ming Sun, X U Daojun, Guoping Sun
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引用次数: 0

Abstract

Esophageal cancer, a prevalent malignant neoplasm affecting the digestive system, is characterized by a poor prognosis and high rates of mortality and morbidity. The tripartite motif containing 31 (TRIM31) gene has been implicated in a variety of human cancers. However, little is known about its phenotypic expression and mechanistic role in esophageal cancer progression. Our study revealed that TRIM31 is highly expressed in esophageal cancer. Loss-of-function analysis demonstrated that TRIM31 depletion inhibited esophageal cancer cell proliferation while suppressing tumor growth and promoting apoptosis in vivo. Furthermore, silencing TRIM31 significantly inhibited migration and invasion while modulating the expression of epithelial-mesenchymal transition (EMT)-related markers. Mechanistically, gamma-butyrobetaine dioxygenase (BBOX1) is predicted to be a downstream gene of TRIM31 and is downregulated in esophageal cancers. TRIM31 enhances the proliferation, migration, and invasion of Eca109 cells through the ubiquitination of BBOX1. In conclusion, TRIM31 functions as an oncogene, suggesting its potential as a novel therapeutic target or prognostic biomarker for patients with esophageal cancer.

E3泛素连接酶TRIM31通过BBOX1的泛素化促进食管癌的进展。
食管癌是一种常见的影响消化系统的恶性肿瘤,其特点是预后差,死亡率和发病率高。含有31 (TRIM31)基因的三方基序与多种人类癌症有关。然而,对其在食管癌进展中的表型表达和机制作用知之甚少。我们的研究发现TRIM31在食管癌中高表达。功能缺失分析表明,TRIM31缺失抑制食管癌细胞增殖,同时抑制肿瘤生长,促进细胞凋亡。此外,沉默TRIM31可显著抑制迁移和侵袭,同时调节上皮-间质转化(epithelial-mesenchymal transition, EMT)相关标志物的表达。从机制上讲,伽马-丁甜菜碱双加氧酶(BBOX1)预计是TRIM31的下游基因,在食管癌中下调。TRIM31通过BBOX1的泛素化促进Eca109细胞的增殖、迁移和侵袭。综上所述,TRIM31具有致癌基因的功能,可能成为食管癌患者新的治疗靶点或预后生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cellular signalling
Cellular signalling 生物-细胞生物学
CiteScore
8.40
自引率
0.00%
发文量
250
审稿时长
27 days
期刊介绍: Cellular Signalling publishes original research describing fundamental and clinical findings on the mechanisms, actions and structural components of cellular signalling systems in vitro and in vivo. Cellular Signalling aims at full length research papers defining signalling systems ranging from microorganisms to cells, tissues and higher organisms.
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