| Literature DB >> 25434519 |
Xiao-Jian Han1, Zhang-Jian Yang1, Li-Ping Jiang2, Yong-Fang Wei1, Ming-Fang Liao1, Yisong Qian1, Yong Li1, Xuan Huang1, Jian-Bin Wang1, Hong-Bo Xin1, Yu-Ying Wan1.
Abstract
Mitochondria are high dynamic organelles with frequent fission and fusion. Here, we found hypoxia stimulated Drp1 expression, mitochondrial fission and migration in metastatic MDA-MB‑231 cells, but not in non-metastatic MCF-7 cells. Inhibition of Drp1-dependent mitochondrial fission by Mdivi-1 or silencing Drp1 attenuated hypoxia-induced mitochondrial fission and migration in MDA-MB‑231 cells. On the other hand, cisplatin induced significant apoptosis and mitochondrial fission in MDA-MB‑231 cells, but not in MCF-7 cells. Mdivi-1 and silencing Drp1 also efficiently prevented cisplatin-induced MMP decrease, ROS production and apoptosis in MDA-MB‑231 cells. Our data suggest that Drp1-dependent mitochondrial fission not only regulates hypoxia-induced migration of breast cancer cells, but also facilitates its sensitivity to chemotherapeutic agents. Thus, targeting Drp1-dependent mitochondrial dynamics may provide a novel strategy to suppress breast cancer metastasis and improve the chemotherapeutic effect in the future.Entities:
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Year: 2014 PMID: 25434519 DOI: 10.3892/ijo.2014.2781
Source DB: PubMed Journal: Int J Oncol ISSN: 1019-6439 Impact factor: 5.650