HMOX1型
血红素加氧酶
化学
癌症研究
癌细胞
血红素
转铁蛋白
下调和上调
纳米点
生物物理学
细胞生物学
生物化学
癌症
生物
基因
物理化学
酶
遗传学
作者
Jianqi Zhao,Yin Chen,Tainong Xiong,Songling Han,Chenwenya Li,Yingjuan He,Yongwu He,Gaomei Zhao,Tao Wang,Liting Wang,Tianmin Cheng,Cheng Wang,Junping Wang
出处
期刊:Small
[Wiley]
日期:2023-01-10
卷期号:19 (10): e2206415-e2206415
被引量:61
标识
DOI:10.1002/smll.202206415
摘要
accumulation and ferroptosis initiation. Furthermore, upregulated nuclear factor erythroid 2-related factor 2 (NRF2), arising from the reduction in Kelch-like ECH-associated protein 1 (KEAP1) expression, is responsible for HMOX1 enhancement after iCoDMSN treatment. Owing to intensified ferroptosis, iCoDMSN acts as an efficient radiotherapy enhancer to eliminate cancer cells in vitro and in vivo. This study demonstrates a versatile Co-based nanomaterial that primes ferroptosis by expanding the labile iron pool in cancer cells, providing a promising tumor radiotherapy sensitizer.
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