体内
程序性细胞死亡
超分子化学
细胞凋亡
诱导剂
脂肽
体外
化学
癌细胞
细胞生物学
生物物理学
生物
生物化学
癌症
细菌
晶体结构
生物技术
基因
遗传学
结晶学
作者
Jiao Lu,Wei Tao Huang,Kexuan Zhou,Xiaoli Zhao,Shu‐Qing Yang,Liqiu Xia,Xuezhi Ding
出处
期刊:Small
[Wiley]
日期:2021-11-11
卷期号:18 (3): e2104034-e2104034
被引量:16
标识
DOI:10.1002/smll.202104034
摘要
Discovering new drugs and improving action mechanisms is a promising strategy to overcome chemotherapy ineffectiveness caused by cancer cell apoptosis resistance. Natural products (like cyclic lipopeptides, CLPs) are potential sources of nonapoptotic cell death inducers and can form diverse supramolecular structures, closely relating to their bioactivities. Herein, it is found for the first time that fatty chain is the key to maintain self-assembled form and antitumor activity of microbial-derived amphiphilic CLP bacillomycin Lb (B-Lb). Compared with B-Lb analogues assemblies without antitumor activity, B-Lb supramolecular self-assemblies (including nanomicelles, nanofibers, giant micrometer rods) can be generated in a multilevel and cross-scale manner and served as a methuosis-like cell death inducer triggered by cytoplasmic vacuolation through macropinocytosis in MDA-MB-231-Luc and MCF-7 cells and in vivo tumor-bearing mice. This study will promote constructing of customized CLP micro-/nanostructures with multipurposes and functions, and boost designing of new antitumor drugs as nonapoptotic cell death modulators based on structure-activity relationship.
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