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gga-miR-155 通过靶向 RORA 对马立克氏病病毒(MDV)转化细胞系 MSB1 的细胞增殖、凋亡和侵袭的影响。

Effect of gga-miR-155 on cell proliferation, apoptosis and invasion of Marek's disease virus (MDV) transformed cell line MSB1 by targeting RORA.

机构信息

Key Laboratory of Animal Disease and Public Health, Henan University of Science and Technology, Luoyang, 471003, People's Republic of China.

出版信息

BMC Vet Res. 2020 Jan 28;16(1):23. doi: 10.1186/s12917-020-2239-4.

Abstract

BACKGROUND

Marek's disease (MD) is caused by the oncogenic Marek's disease virus (MDV), and is a highly contagious avian infection with a complex underlying pathology that involves lymphoproliferative neoplasm formation. MicroRNAs (miRNAs) act as oncogenes or tumor suppressors in most cancers. The gga-miR-155 is downregulated in the MDV-infected chicken tissues or lymphocyte lines, although its exact role in tumorigenesis remains unclear. The aim of this study was to analyze the effects of gga-miR-155 on the proliferation, apoptosis and invasiveness of an MDV-transformed lymphocyte line MSB1 and elucidate the underlying mechanisms.

RESULTS

The expression level of gga-miR-155 was manipulated in MSB1 cells using specific mimics and inhibitors. While overexpression of gga-miR-155 increased proliferation, decreased the proportion of G1 phase cells relative to that in S and G2 phases, reduced apoptosis rates and increased invasiveness. However, its downregulation had the opposite effects. Furthermore, gga-miR-155 directly targeted the RORA gene and downregulated its expression in the MSB1 cells.

CONCLUSION

The gga-miR-155 promotes the proliferation and invasiveness of the MDV-transformed lymphocyte line MSB1 and inhibits apoptosis by targeting the RORA gene.

摘要

背景

马立克氏病(MD)是由致癌性马立克氏病病毒(MDV)引起的,是一种具有复杂潜在病理学的高度传染性禽类感染,涉及淋巴增生性肿瘤的形成。MicroRNAs(miRNAs)在大多数癌症中充当癌基因或肿瘤抑制因子。gga-miR-155 在感染 MDV 的鸡组织或淋巴细胞系中下调,尽管其在肿瘤发生中的确切作用仍不清楚。本研究旨在分析 gga-miR-155 对 MDV 转化的淋巴细胞系 MSB1 的增殖、凋亡和侵袭的影响,并阐明其潜在机制。

结果

使用特异性模拟物和抑制剂来操纵 MSB1 细胞中的 gga-miR-155 表达水平。gga-miR-155 的过表达增加了增殖,降低了 S 和 G2 期细胞相对于 G1 期的比例,降低了凋亡率并增加了侵袭性。然而,其下调则有相反的效果。此外,gga-miR-155 直接靶向 RORA 基因并下调了 MSB1 细胞中的表达。

结论

gga-miR-155 通过靶向 RORA 基因促进 MDV 转化的淋巴细胞系 MSB1 的增殖和侵袭,并抑制凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5162/6988224/dcc8d4424c87/12917_2020_2239_Fig1_HTML.jpg

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