免疫系统
免疫疗法
癌症研究
结直肠癌
免疫原性细胞死亡
下调和上调
医学
癌细胞
癌症
肿瘤微环境
阿霉素
化疗
免疫学
生物
内科学
生物化学
基因
作者
Linping Zhao,Rongrong Zheng,Xiaona Rao,Chu‐Yu Huang,Hangyu Zhou,Xi‐Yong Yu,Xueyan Jiang,Shiying Li
标识
DOI:10.1002/advs.202309204
摘要
The chemo-regulation abilities of chemotherapeutic medications are appealing to address the low immunogenicity, immunosuppressive lactate microenvironment, and adaptive immune resistance of colorectal cancer. In this work, the proteolysis targeting chimera (PROTAC) of BRD4 (dBET57) is found to downregulate colorectal cancer glycolysis through the transcription inhibition of c-Myc, which also inhibits the expression of programmed death ligand 1 (PD-L1) to reverse immune evasion and avoid adaptive immune resistance. Based on this, self-delivery nano-PROTACs (designated as DdLD NPs) are further fabricated by the self-assembly of doxorubicin (DOX) and dBET57 with the assistance of DSPE-PEG
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