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

被引:2
|
作者
Min, Liangliang [1 ]
Chen, Lu [1 ]
Huang, Da [1 ]
Zhang, Yulu [1 ,2 ]
You, Aihua [3 ]
Yan, Xiaohua [1 ,4 ]
Li, Zhi-hua [1 ,2 ,3 ]
机构
[1] Third Hosp Nanchang, Jiangxi Prov Key Lab Breast Dis 2024SSY06221, Nanchang 330009, Jiangxi, Peoples R China
[2] Third Hosp Nanchang, Dept Breast Surg, Nanchang 330009, Jiangxi, Peoples R China
[3] Jiangxi Univ Tradit Chinese Med, Nanchang 330004, Jiangxi, Peoples R China
[4] Nanchang Univ, Jiangxi Med Coll, Sch Basic Med Sci, Nanchang 330031, Jiangxi, Peoples R China
关键词
LncRNAs; HIF1A-AS2; MRPS23; TNBC; Paclitaxel resistance;
D O I
10.1016/j.heliyon.2024.e36469
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:15
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