内质网相关蛋白降解
内质网
癌症研究
未折叠蛋白反应
肺癌
化学
细胞生长
细胞培养
细胞生物学
生物
内科学
医学
生物化学
遗传学
作者
Lihuai Wang,Tonglin Sun,Xiao Yang,Zhi Wen,Yinhui Sun,Hua Liu
出处
期刊:Current Computer - Aided Drug Design
[Bentham Science]
日期:2024-01-17
卷期号:20
被引量:1
标识
DOI:10.2174/0115734099252873231117072107
摘要
Background:: Astragaloside IV (AS-IV) has been shown to have a curative effect on non-small cell lung cancer (NSCLC). This study aimed to elucidate the role of AS-IV in NSCLC cell anlotinib resistance (AR). Methods:: The NSCLC/AR cells, resistant to anlotinib, have been produced. The role of AS-IV in the AR of NSCLC cells about the miR-181a-3p/unfolded protein response (UPR)- endoplasmic reticulum associated degradation (ERAD) pathway was then discussed by treating the cells with anlotinib or AS-IV, or by manipulating them with inhibitors or mimics of miR- 181a-3p, HRD1 or Derlin-1 overexpression plasmids. Results:: We found that AS-IV could suppress the AR of NSCLC cells. In addition, miR-181a- 3p was elevated in NSCLC/AR cells. Functionally, AS-IV limited the AR of NSCLC cells by reducing miR-181a-3p. Further, activation of the UPR-ERAD pathway was correlated with AR in NSCLC cells. Increased sensitivity of NSCLC cells to anlotinib caused by miR-181a-3p inhibitor could be reversed by overexpression of HRD1 or Derlin-1. Conclusion:: This research revealed a promising NSCLC/AR treatment approach by showing that AS-IV exposed NSCLC cells to anlotinib by inhibiting the miR-181a-3p/UPR-ERAD axis.
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