胶质母细胞瘤
纳米棒
手性(物理)
体内
癌症研究
材料科学
生物相容性材料
信号转导
纳米技术
MAPK/ERK通路
基因
对映体
细胞生物学
癌症
体外
下调和上调
胶质瘤
癌细胞
基因表达
生物物理学
磷酸化
脑瘤
生物
基因表达调控
化学
作者
Zhi Qian Tong,Nan Li,Xueru Guo,Mingjiang Zhang,Bo Li,Shanshan Zhao,Chong Zhang,Yan Jiang,Qi Guo,RAN Shan,Yajie Zhou,Kewenjing Zhu,Yun Huang,Nian Zou,Mohan Wang,Kan He,Tongcui Jiang,Tao‐Tao Zhuang
标识
DOI:10.1002/adfm.202527480
摘要
ABSTRACT Glioblastoma—the most aggressive and lethal primary brain malignancy—is pathologically associated with aberrant enantiomeric ratios of amino acids. This chiral imbalance catalyzes the exploration of leveraging chirality in nano‐engineering glioblastoma therapy; yet, it remains unproven due to challenges in precise regulation and in‐depth understanding of chirality‐neuro system interactions. Herein, we propose a helix‐and‐modification‐of‐surface‐atoms strategy, producing biocompatible chiral gold nanorods with intrinsic nanohelical morphology. The strong and tunable chiroptical activity selectively upregulates key pro‐apoptotic genes while downregulating certain pro‐proliferative ones, demonstrating nanoscaled chirality‐dependent glioblastoma suppression. Notably, in vivo evolutions show that right‐handed helices exhibit potent inhibition of PI3K‐Akt and MAPK signaling cascades, resulting in an 81.2% reduction in intracranial tumor area compared to their left‐handed counterparts. These findings reveal that chirality‐engineered gold nanorods enantioselectively modulate gene expression and inhibit critical signaling pathways activated in cancer cells, providing a novel therapeutic avenue for glioblastoma and beyond.
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