癌细胞
氧化应激
细胞凋亡
活性氧
材料科学
细胞生物学
光热治疗
癌症研究
癌症
化学
纳米技术
生物
生物化学
遗传学
作者
Boying Li,Shuxi Ren,Dong Gao,Ning Li,Manman Wu,Hongbo Yuan,Mei Zhou,Chengfen Xing
标识
DOI:10.1002/adhm.202102506
摘要
Abstract Cancer cells survive by relying on oxidative stress defense against the accumulation of reactive oxygen species (ROS) during tumor formation. ROS‐sensitive TRPA1 ion channels are overexpressed in breast cancer cells and induce a large influx of Ca 2+ which upregulates the anti‐apoptotic pathway to lead breast cancer cells to produce oxidative stress defense and enhance the resistance to ROS related chemotherapy. Targeting and inhibiting the TRPA1 ion channels are critical for breaking down the oxidative stress defense system and overcoming cellular resistance. Here, near‐infrared (NIR) light‐responsive conjugated polymer nanoparticles are designed and prepared to promote apoptosis of breast cancer cells, reduce cell drug resistance and suppress tumor growth through the remote and precise regulation of TRPA1 ion channels. Upon 808 nm laser irradiation, the nanoparticles block the formation of Ca 2+ /CaM complex and regulate the content of MCL‐1 protein. Especially, the nanoparticles overcome drug resistance of cancer cells, therefore accelerating apoptosis of cancer cells and suppressing tumor growth in mice. Compared with carboplatin, the volume of tumor induced by NPs‐H decreases by 54.1%. This work provides a strategy to disrupt the oxidative stress defense system and downregulate the antiapoptotic signaling pathway in cancer cells.
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