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硬脂酰辅酶 A 去饱和酶 1 是 EBV 编码的 miR-BART20-5p 的靶标,调节 EBV 相关胃癌中的细胞自噬、增殖和迁移。

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

机构信息

Department of Pathogenic Biology, School of Basic Medicine, Qingdao University, Qingdao, 266071, China.

Department of Pathology of the Affiliated Hospital of Qingdao University, 16 Jiangsu Road, Qingdao, 266003, China.

出版信息

Virus Genes. 2024 Oct;60(5):464-474. doi: 10.1007/s11262-024-02094-3. Epub 2024 Aug 3.

Abstract

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.

摘要

EB 病毒(EBV)是已知的第一个表达 microRNAs(miRNAs)的人类致癌病毒,miRNAs 与包括鼻咽癌和胃癌在内的各种肿瘤的发展密切相关。硬脂酰辅酶 A 去饱和酶 1(SCD1)是脂肪酸合成中的关键酶,在许多肿瘤中高表达,促进肿瘤生长和转移,使其成为潜在的治疗靶点。在这项研究中,我们发现在细胞和组织水平上,EBV 相关胃癌(EBVaGC)中 SCD1 的表达明显低于 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 通过靶向 SCD1 可能促进 EBVaGC 的进展。

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