泛诺比司他(LBH589)联合AM1241通过自噬途径诱导宫颈癌症细胞凋亡。

IF 2.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Bo Sheng, Wenwen Wang, Dongyue Xia, Xiangdong Qu
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引用次数: 0

摘要

目的:研究LBH589与选择性CB2受体激动剂AM1241联合治疗对宫颈癌症细胞凋亡的影响,阐明联合治疗的机制,为该病的治疗提供创新策略。方法:采用细胞计数试剂盒-8(CCK-8)法测定宫颈癌症细胞的活力,并用SynergyFinder分析其协同效应。通过细胞克隆检测细胞增殖。用流式细胞术分析宫颈癌症细胞凋亡和活性氧(ROS)的产生。采用蛋白质印迹和实时定量PCR(qRT-PCR)测定通路相关因子的蛋白质和基因水平的变化。结果:根据细胞毒性测定结果,筛选出SiHa细胞,并用0.1μM LBH589和4μM AM1241处理24小时,用于后续实验。根据bliss、ZIP、HSA和LOEWE协同得分确定,两者的组合是协同的。平板克隆结果表明,与单独的药物相比,LBH589与AM1241联合抑制了宫颈癌症细胞的增殖。此外,与单独的LBH589相比,LBH589和AM1241的组合通过增加LC3II/LC3I和减少P62/GAPDH来诱导自噬,导致显著更高的细胞凋亡率。药理学抑制也抑制细胞凋亡。一致地,我们发现内质网、DNA损伤修复途径在联合给药后被诱导。此外,共给药后,细胞ROS增加,添加ROS清除剂可抑制细胞凋亡。结论:LBH589联合AM1241激活内质网应急通路、DNA损伤修复信号通路、氧化应激和自噬通路,最终促进宫颈癌症细胞凋亡。这些发现表明,LBH589和AM1241的联合给药可能是治疗宫颈癌症的一种新的治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Panobinostat (LBH589) combined with AM1241 induces cervical cancer cell apoptosis through autophagy pathway.

Purpose: The study aims to investigate the apoptotic effects of combining LBH589 and AM1241 (a selective CB2 receptor agonist) on cervical cancer cells and elucidating the mechanism of this combined therapy, which may provide innovative strategies for treating this disease.

Methods: The viability of the cervical cancer cells was measured by cell counting kit-8 (CCK-8) assay, and the synergistic effect was analyzed using SynergyFinder. Cell proliferation was tested by cell cloning. The apoptosis and reactive oxygen species (ROS) production in cervical cancer cells were analyzed by flow cytometry. Western blot and quantitative real-time PCR (qRT-PCR) were employed to determine changes in protein and gene levels of pathway-related factors.

Results: By the results of cytotoxicity assay, SiHa cells were selected and treated with 0.1 μM LBH589 and 4 μM AM1241 for 24 h for subsequent experiments. The combination of both was synergistic as determined by bliss, ZIP, HSA and LOEWE synergy score. Plate cloning results showed that LBH589 combined with AM1241 inhibited the proliferation of cervical cancer cells compared to individual drug. Additionally, compared with LBH589 alone, the combination of LBH589 and AM1241 induced autophagy by increasing LC3II/LC3I and decreasing P62/GAPDH, leading to a significantly higher rate of apoptosis. Pharmacological inhibition of also inhibited apoptosis. Consistently, we found that the endoplasmic reticulum, DNA damage repair pathway were induced after co-administration. Furthermore, cellular ROS increased after co-administration, and apoptosis was inhibited by the addition of ROS scavenger.

Conclusion: LBH589 combined with AM1241 activated the endoplasmic reticulum emergency pathway, DNA damage repair signaling pathway, oxidative stress and autophagy pathway, ultimately promoting the apoptosis of cervical cancer cells. These findings suggest that the co-administration of LBH589 and AM1241 may be a new treatment plan for the treatment of cervical cancer.

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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACYTOXICOLOGY&nb-TOXICOLOGY
CiteScore
4.80
自引率
0.00%
发文量
87
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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