自噬
三阴性乳腺癌
细胞凋亡
癌症研究
流式细胞术
活力测定
化学
MTT法
免疫印迹
癌细胞
乳腺癌
癌症
生物
分子生物学
生物化学
基因
遗传学
作者
Xia Cao,Chien‐Wei Chen,Kai Yin,Tzong‐Luen Wang,Yao‐Kuang Huang,Pang‐Yen Chen,Po‐Hua Su
摘要
ABSTRACT Triple negative breast cancer (TNBC) is characterized by high heterogenicity and aggressiveness and autophagy plays a complicated role in cancer development. Zingerone is reported to possess multiple pharmacological activities, including antitumors. This study explored the biological role and the relevant mechanisms of zingerone in TNBC. Following zingerone treatment, the viability of normal breast cancer cells MCF‐10A and TNBC cells (MDA‐MB‐231 and MDA‐MB‐468) was detected with CCK‐8 assay. The proliferation, migration and invasion of TNBC cells were detected with colony formation, wound healing, and transwell assays. Western blot was used to detect the expressions of migration‐, apoptosis‐ and autophagy‐related proteins. Flow cytometry was used to detect the cell apoptotic level and immunofluorescence assay measured the autophagy. The experimental data revealed that zingerone with varying concentrations suppressed cell viability, proliferation, migration and invasion while promoting the apoptosis in TNBC, which might be mediated by autophagy activation. Besides, zingerone decreased HDAC1 expression in TNBC cells and regulated autophagy via HDAC1. Collectively, zingerone impeded the malignant progression of TNBC via inducing HDAC1‐mediated autophagy.
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