Pulsatilla saponin E suppresses viability, migration, invasion and promotes apoptosis of NSCLC cells through negatively regulating Akt/FASN pathway via inhibition of flotillin-2 in lipid raft.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Receptors and Signal Transduction Pub Date : 2022-02-01 Epub Date: 2020-11-26 DOI:10.1080/10799893.2020.1839764
Minghua Zhu, Wei Shi, Ke Chen, Huiqun Hu, Xiangqing Ye, Yinfang Jiang
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引用次数: 4

Abstract

Purpose: Pulsatilla saponins from pulsatilla chinensis (Bunge) Regel have potential anti-tumor activities to certain human cancers. However, the roles of pulsatilla saponin E separated from pulsatilla saponins in non-small cell lung cancer (NSCLC) have not been reported.

Materials and methods: After treating NSCLC cells by pulsatilla saponin E at different concentrations, cell viability was measured by MTT and CCK-8 assays, and cell migration, invasion and apoptosis were detected by scratch wound-healing, transwell and flow cytometry assays. The contents of free cholesterol (FC) and total cholesterol (TC) were measured by high performance liquid chromatography (HPLC). The expression levels of flotillin-1, flotillin-2, Akt, fatty acid synthase (FASN) were detected by qRT-PCR and Western blot assays.

Results: Pulsatilla saponin E suppressed viability, migration, invasion and promoted apoptosis of NSCLC cells followed by regulation of apoptosis-related proteins, reduced contents of FC and TC, and the expression levels of flotillin-1, flotillin-2, Akt, and FASN in a concentration-dependent manner. However, the inhibitory effects of pulsatilla saponin E on viability, migration, invasion of A549 cells and the expression levels of flotillin-1, flotillin-2, Akt, and FASN were reversed by flotillin-2 overexpression.

Conclusions: Our study revealed that pulsatilla saponin E suppressed migration, invasion and promoted apoptosis of NSCLC cells through negatively regulating Akt/FASN signaling pathway via the inhibition of flotillin-2 in lipid raft (LR). The current findings could be explored for developing a novel therapeutic drug for NSCLC treatment.

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白头翁皂苷E通过抑制脂筏中的flotilin -2负调控Akt/FASN通路,抑制NSCLC细胞的生存、迁移、侵袭,促进细胞凋亡。
目的:白头翁皂苷对某些人类肿瘤具有潜在的抗肿瘤活性。然而,白头翁皂苷E在非小细胞肺癌(NSCLC)中的作用尚未见报道。材料与方法:不同浓度白头翁皂苷E处理NSCLC细胞后,采用MTT和CCK-8检测细胞活力,采用划痕创面愈合、transwell和流式细胞术检测细胞迁移、侵袭和凋亡。采用高效液相色谱法测定游离胆固醇(FC)和总胆固醇(TC)的含量。采用qRT-PCR和Western blot检测flotilin -1、flotilin -2、Akt、脂肪酸合成酶(FASN)的表达水平。结果:白芍总皂苷E抑制NSCLC细胞活力、迁移、侵袭,促进细胞凋亡,进而调控凋亡相关蛋白,降低FC、TC含量,降低flotilin -1、flotilin -2、Akt、FASN表达水平,且呈浓度依赖性。然而,白白花皂苷E对A549细胞的活力、迁移、侵袭以及flotillin-1、flotillin-2、Akt、FASN表达水平的抑制作用被flotillin-2过表达逆转。结论:本研究发现白芍皂苷E通过抑制脂质筏(LR)中的flotilin -2负调控Akt/FASN信号通路,抑制NSCLC细胞的迁移、侵袭并促进细胞凋亡。目前的研究结果可以为开发一种新的治疗非小细胞肺癌的药物进行探索。
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来源期刊
Journal of Receptors and Signal Transduction
Journal of Receptors and Signal Transduction 生物-生化与分子生物学
CiteScore
6.60
自引率
0.00%
发文量
19
审稿时长
>12 weeks
期刊介绍: Journal of Receptors and Signal Tranduction is included in the following abstracting and indexing services: BIOBASE; Biochemistry and Biophysics Citation Index; Biological Abstracts; BIOSIS Full Coverage Shared; BIOSIS Previews; Biotechnology Abstracts; Current Contents/Life Sciences; Derwent Chimera; Derwent Drug File; EMBASE; EMBIOLOGY; Journal Citation Reports/ Science Edition; PubMed/MedLine; Science Citation Index; SciSearch; SCOPUS; SIIC.
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