氧化磷酸化
流式细胞术
细胞凋亡
柠檬酸循环
线粒体
线粒体生物发生
细胞生物学
蛋白质组学
糖酵解
细胞
化学
癌症研究
三阴性乳腺癌
新陈代谢
癌细胞
磷酸化
细胞周期
生物
生物化学
癌症
乳腺癌
分子生物学
基因
遗传学
作者
Jiefeng Zhou,Qingcao Li,Haoran Wu,Shin‐Han Tsai,Yu-Ting Yeh
标识
DOI:10.2174/1570164618666210208144542
摘要
Background : Triple-negative breast cancer (TNBC) is a subtype of invasive cancer in breast with the symptoms of unfavourable prognosis and limited targeted treatment options. Evidence of changes in the metabolic status of TNBC, characterised by increased glycolysis, mitochondrial oxidative phosphorylation, as well as production and utilization of tricarboxylic acid cycle intermediates. Objective: Investigate the proteins altered in cryptotanshinone treated MDA-MB-231 cells and explore the key pathways and specific molecular markers involved in cryptotanshinone treatment. Method: We use unlabeled quantitative proteomics to gain insight into the anticancer mechanism of cryptotanshinone on MDA-MB231 triple negative breast cancer cells. And flow cytometry was used to detect apoptosis and changes in cell mitochondrial membrane potential. Results: We show that inhibiting the expression of electron transport chain complex proteins, also inhibits mitochondrial oxidative phosphorylation. Additionally, down-regulation of the ribosime biogenesis pathway was found to inhibit cell metabolism. Conclusion: In summary, results show that cryptotanshinone can trigger rapid and irreversible apoptosis in MDA-MB-231 cells through effectively inhibiting cell metabolism.
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