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Novel Mitochondria-Targeted NIR Cyanine Cy750M-C1 Nanoparticles for Chemotherapy against Triple-Negative Breast Cancer

三阴性乳腺癌 乳腺癌 化疗 癌症研究 纳米颗粒 材料科学 医学 癌症 肿瘤科 纳米技术 内科学 荧光 物理 量子力学
作者
Zhi-Lin Shen,Fenglin Zhang,Jiawang Yang,Kaihang Zhang,Feng Liang,Han Mu,Shi Li,Ji‐Jun Jiang,Yuanzhi Yang,Zhixuan Lin,Jie Gao,Ning Gao
出处
期刊:ACS Biomaterials Science & Engineering [American Chemical Society]
卷期号:11 (6): 3738-3751 被引量:1
标识
DOI:10.1021/acsbiomaterials.5c00343
摘要

Mitochondrial metabolism plays an important role in promoting cancer development, making mitochondria a novel promising target for cancer therapy. Current mitochondria-targeted fluorescent agents can specifically accumulate in the mitochondria of cancer cells and can be applied for cancer imaging and therapy. However, their clinical application is still limited due to the poor solubility and lower tumor-specific distribution. In the present study, we synthesized a novel NIR small-molecule dye, Cy750M-C1, and evaluated its optical properties, mitochondrial distribution, and anticancer activity. We also synthesized nanoparticles loading Cy750M-C1 (Cy750M-C1-FA-NPs) and demonstrated that Cy750M-C1-FA-NPs are specifically targeted to the tumor and dramatically inhibited tumor growth in vivo. The mechanistic study revealed that Cy750M-C1 specifically targeted mitochondria of TNBC cells, subsequently promoting ROS production through inhibition of mitochondrial complexes (complexes I, III, and IV) and OXPHOS and depletion of ATP, leading, in turn, to AMPK activation and Drp1 dephosphorylation mediating the mitochondrial translocation of Drp1 and BAX and ultimately inducing mitochondrial fission, caspase activation, as well as apoptosis. Overall, our data implicate that Cy750M-C1 could be developed as a novel anticancer agent with mitochondria-targeting ability and NIR fluorescence imaging and that Cy750M-C1-FA-NPs could also be considered as promising drug delivery carriers for antitumor agents.
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