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长链非编码RNA HIF1A-AS2通过MRPS23蛋白促进三阴性乳腺癌进展和紫杉醇耐药。

LncRNA HIF1A-AS2 promotes triple-negative breast cancer progression and paclitaxel resistance via MRPS23 protein.

作者信息

Min Liangliang, Chen Lu, Huang Da, Zhang Yulu, You Aihua, Yan Xiaohua, Li Zhi-Hua

机构信息

Jiangxi Province Key Laboratory of Breast Diseases (No.2024SSY06221), Third Hospital of Nanchang, Jiangxi, 330009, China.

Department of Breast Surgery, Third Hospital of Nanchang, Jiangxi, 330009, China.

出版信息

Heliyon. 2024 Aug 16;10(17):e36469. doi: 10.1016/j.heliyon.2024.e36469. eCollection 2024 Sep 15.

Abstract

Dysregulation of lncRNAs is a critical factor in the migration and invasion of tumors. Here our study reveals that lncRNA HIF1A-AS2 is highly expressed in breast cancer tissues and various TNBC cell lines. Moreover, we present compelling evidence supporting the role of HIF1A-AS2 in promoting TNBC cell proliferation, metastasis, invasion, and resistance to paclitaxel treatment. Additionally, our transcriptome sequencing analysis identifies MRPS23 as a potential downstream target protein regulated by HIF1A-AS2 and knockdown of HIF1A-AS2 leads to decreased expression of MRPS23 in TNBC cells. Moreover, MRPS23 exhibits similar effects on enhancing cell proliferation, metastasis, invasion, and paclitaxel resistance in TNBC cells. Furthermore, downregulating HIF1A-AS2 suppresses the enhanced functionality observed in TNBC cells due to upregulated MRPS23 expression. These findings suggest that modulation of MRPS23 protein expression by HIF1A-AS2 may influence cellular processes and paclitaxel sensitivity in TNBC cells.

摘要

长链非编码RNA(lncRNAs)的失调是肿瘤迁移和侵袭的关键因素。我们的研究表明,lncRNA HIF1A-AS2在乳腺癌组织和各种三阴性乳腺癌(TNBC)细胞系中高表达。此外,我们提供了有力证据,支持HIF1A-AS2在促进TNBC细胞增殖、转移、侵袭以及对紫杉醇治疗耐药方面的作用。此外,我们的转录组测序分析确定MRPS23是受HIF1A-AS2调控的潜在下游靶蛋白,敲低HIF1A-AS2会导致TNBC细胞中MRPS23表达降低。此外,MRPS23在增强TNBC细胞增殖、转移、侵袭和紫杉醇耐药性方面表现出类似作用。此外,下调HIF1A-AS2可抑制由于MRPS23表达上调而在TNBC细胞中观察到的功能增强。这些发现表明,HIF1A-AS2对MRPS23蛋白表达的调节可能影响TNBC细胞的细胞过程和紫杉醇敏感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df1/11403533/de5f3e4bd411/gr1.jpg

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