癌症研究
化学
蛋白激酶B
吉西他滨
内吞作用
细胞生物学
激酶
PI3K/AKT/mTOR通路
信号转导
蛋白激酶A
抗药性
克拉斯
胰腺癌
细胞
下调和上调
帕博西利布
配体(生物化学)
P110α
视网膜母细胞瘤蛋白
癌基因
多重耐药
细胞毒性
生物
药品
卡波扎尼布
药理学
药物发现
细胞生长
紫杉醇
癌症
作者
Zhen Jiang,Yi Pan,Gengqi Liu,He Ren,Yumiao Zhang
标识
DOI:10.1021/acsabm.5c02218
摘要
Pancreatic ductal adenocarcinoma (PDAC) represents one of the deadliest malignancies as KRAS (Kirsten rat sarcoma viral oncogene homolog) mutations continuously activate multiple downstream signaling pathways, leading to drug resistance. To overcome this issue, herein, we developed a cobalt-pheophytin (CoPheo) coordination micelle chelating two chemotherapeutic agents including ONC201 and Palbociclib (Pal), yielding CoPheo-ONC201-Pal-F127. Compared with other metals, cobalt exhibits stronger coordination ability and higher drug-loading efficiency. The resulting ligand bonds are both acid- and GSH-responsive so that the cargos could be responsively released in the tumor microenvironment. To overcome drug resistance in KRAS-mutant cancers, CoPheo-ONC201-Pal-F127 is able to regulate three independent cell death pathways including ferroptosis, disulfidptosis, and cellular senescence. In particular, the cobalt-mediated Fenton-like effect synergistically enhances ONC201-induced serine-threonine protein kinase AKT (AKT) inhibition to amplify ferroptosis. Also, cobalt-mediated NADPH oxidation disrupts redox homeostasis in synergy with Pal-induced NADPH depletion, triggering disulfidptosis. In addition, ONC201-mediated mitogen-activated protein kinase kinase (MEK) inhibition, combined with Pal-induced CDK4/6 blockade, promotes cellular senescence and remodels the tumor microenvironment. These three independent mechanisms collectively establish a mutually enhanced therapeutic strategy capable of overcoming the complex drug resistance driven by multiple downstream signaling pathways in KRAS-mutant pancreatic cancer.
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