癌症研究
三阴性乳腺癌
纳米载体
胰腺癌
化疗
医学
癌症
细胞凋亡
免疫系统
乳腺癌
DU145型
转移性乳腺癌
阿霉素
癌细胞
转移
细胞毒性T细胞
活性氧
化学
基质金属蛋白酶
谷胱甘肽
细胞毒性
细胞内
肿瘤微环境
免疫原性细胞死亡
循环肿瘤细胞
小发夹RNA
炎症
程序性细胞死亡
小RNA
内科学
细胞
免疫疗法
肿瘤科
放射治疗
弹性蛋白酶
生物
作者
Yanming Xia,Shuxian Xu,Yutong Wu,Xiaochun Ma,Linxiu Peng,You Lü,Xiaopeng Han,Chao Qin,Lifang Yin
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-01-26
卷期号:20 (5): 4166-4180
标识
DOI:10.1021/acsnano.5c16112
摘要
OH. CB-839 impedes mitochondrial GSH biosynthesis, enhances PPE-mediated hydrolysis and CD95 death domain release, and drives reactive oxygen species buildup in tumor cells. Furthermore, the combined action of PPE and CB-839 leads to lipid peroxide accumulation, mitochondrial collapse, and intensified tumor cell apoptosis. This multifunctional nanoplatform achieves strong tumor suppression and initiates immunogenic cell death, resulting in immune activation. When applied as a neoadjuvant regimen in conjunction with surgery, PMC@HA significantly decreases postoperative recurrence and distant metastasis in TNBC. This combinatorial approach may improve chemosensitivity and limit metastatic progression, thereby potentially extending long-term survival in patients with TNBC.
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