Mitochondrial dynamics regulates hypoxia-induced migration and antineoplastic activity of cisplatin in breast cancer cells

Xiao‐Jian Han(Nanchang University), Zhang‐Jian Yang(Nanchang University), Liping Jiang(Nanchang University), Yongfang Wei(Nanchang University), Mingfang Liao(Nanchang University), Yisong Qian(Nanchang University), Yong Li(Nanchang University), Xuan Huang(Nanchang University), Jianbin Wang(Nanchang University), HONG-BO XIN(Nanchang University), Yuying Wan(Nanchang University)
International Journal of Oncology
November 27, 2014
Cited by 113Open Access
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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.


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