硬脂酰-CoA 去饱和酶 1 是 EBV 编码的 miR-BART20-5p 的靶标,在 EBV 相关胃癌中调控细胞自噬、增殖和迁移

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY
Zhiyuan Gong, Duo Shi, Zhiyong Yan, Lingling Sun, Wen Liu, Bing Luo
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引用次数: 0

摘要

爱泼斯坦-巴氏病毒(EBV)是已知的第一个表达微RNA(miRNA)的人类致癌病毒,miRNA与包括鼻咽癌和胃癌在内的多种肿瘤的发生密切相关。硬脂酰-CoA 不饱和酶 1(SCD1)是脂肪酸合成的关键酶,在多种肿瘤中高表达,促进肿瘤生长和转移,是潜在的治疗靶点。本研究发现,在细胞和组织水平上,SCD1 在 EBV 相关性胃癌(EBVaGC)中的表达量明显低于 EBV 阴性胃癌(EBVnGC)。此外,EBV-miR-BART20-5p 靶向 SCD1 的 3′-UTR,下调其表达。此外,在 EBVaGC 细胞中过表达 SCD1 可促进细胞迁移和增殖,同时抑制自噬。这些结果表明,EBV编码的miRNA-BART20-5p可能通过靶向SCD1促进EBVaGC的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Stearoyl-CoA desaturase 1 is targeted by EBV-encoded miR-BART20-5p and regulates cell autophagy, proliferation, and migration in EBV-associated gastric cancer

Stearoyl-CoA desaturase 1 is targeted by EBV-encoded miR-BART20-5p and regulates cell autophagy, proliferation, and migration in EBV-associated gastric cancer

Epstein-Barr virus (EBV) is the first human oncogenic virus known to express microRNAs (miRNAs), which are closely associated with the development of various tumors, including nasopharyngeal and gastric cancers. Stearoyl-CoA Desaturase 1 (SCD1) is a key enzyme in fatty acid synthesis, highly expressed in numerous tumors, promoting tumor growth and metastasis, making it a potential therapeutic target. In this study, we found that SCD1 expression in EBV-associated gastric cancer (EBVaGC) was significantly lower than in EBV-negative gastric cancer (EBVnGC) at both cellular and tissue levels. In addition, EBV-miR-BART20-5p targets the 3′-UTR of SCD1, downregulating its expression. Moreover, overexpression of SCD1 in EBVaGC cells promoted cell migration and proliferation while inhibiting autophagy. These results suggest that EBV-encoded miRNA-BART20-5p may contribute to EBVaGC progression by targeting SCD1.

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来源期刊
Virus Genes
Virus Genes 医学-病毒学
CiteScore
3.30
自引率
0.00%
发文量
76
审稿时长
3 months
期刊介绍: Viruses are convenient models for the elucidation of life processes. The study of viruses is again on the cutting edge of biological sciences: systems biology, genomics, proteomics, metagenomics, using the newest most powerful tools. Huge amounts of new details on virus interactions with the cell, other pathogens and the hosts – animal (including human), insect, fungal, plant, bacterial, and archaeal - and their role in infection and disease are forthcoming in perplexing details requiring analysis and comments. Virus Genes is dedicated to the publication of studies on the structure and function of viruses and their genes, the molecular and systems interactions with the host and all applications derived thereof, providing a forum for the analysis of data and discussion of its implications, and the development of new hypotheses.
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