Effective Inhibition of Mitochondrial Metabolism by Cryptotanshinone in MDA-MB231 cells: A Proteomic Analysis

Author:

Zhou Jiefeng1,Li Qingcao2,Wu Haoran3,Tsai Shin-Han4,Yeh Yu-Ting5

Affiliation:

1. Graduate Institute of Biomedical Informatics, College of Medical Science and Technology, Taipei Medical University,- Taipei City, Taiwan | Ningbo AJcore Biosciences Inc., 3rd Floor, Building One, East District, Ningbo New Materials Innovation Center, High-Tech Zone, Ningbo, China

2. Laboratory Department,Ningbo Medical Center Li Huili Eastern Hospital,High-Tech Zone, Bingbo, China

3. Ningbo AJcore Biosciences Inc., 3rd Floor, Building One, East District, Ningbo New Materials Innovation Center, High-Tech Zone, Ningbo, China

4. Department of Emergency Medicine, Shuang Ho Hospital, Taipei Medical University, Institute of Injury Prevention and Control, Taipei Medical University, Taipei City, Taiwan

5. Graduate Institute of Biomedical Informatics, College of Medical Science and Technology, Taipei Medical University,- Taipei City, Taiwan | Information Technology Office, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan

Abstract

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.

Publisher

Bentham Science Publishers Ltd.

Subject

Molecular Biology,Biochemistry

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