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10.3390/ijms160819836

http://scihub22266oqcxt.onion/10.3390/ijms160819836
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C4581328!4581328!26307971
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suck abstract from ncbi


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pmid26307971      Int+J+Mol+Sci 2015 ; 16 (8): 19836-50
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  • Mitochondrial Transcription Factor A and Mitochondrial Genome as Molecular Targets for Cisplatin-Based Cancer Chemotherapy #MMPMID26307971
  • Kohno K; Wang KY; Takahashi M; Kurita T; Yoshida Y; Hirakawa M; Harada Y; Kuma A; Izumi H; Matsumoto S
  • Int J Mol Sci 2015[Aug]; 16 (8): 19836-50 PMID26307971show ga
  • Mitochondria are important cellular organelles that function as control centers of the energy supply for highly proliferative cancer cells and regulate apoptosis after cancer chemotherapy. Cisplatin is one of the most important chemotherapeutic agents and a key drug in therapeutic regimens for a broad range of solid tumors. Cisplatin may directly interact with mitochondria, which can induce apoptosis. The direct interactions between cisplatin and mitochondria may account for our understanding of the clinical activity of cisplatin and development of resistance. However, the basis for the roles of mitochondria under treatment with chemotherapy is poorly understood. In this review, we present novel aspects regarding the unique characteristics of the mitochondrial genome in relation to the use of platinum-based chemotherapy and describe our recent work demonstrating the importance of the mitochondrial transcription factor A (mtTFA) expression in cancer cells.
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