同源盒蛋白纳米
癌症干细胞
替莫唑胺
癌症研究
RNA干扰
生物
PI3K/AKT/mTOR通路
蛋白激酶B
干细胞
癌细胞
细胞周期
癌症
胚胎干细胞
胶质瘤
信号转导
细胞生物学
基因
诱导多能干细胞
遗传学
核糖核酸
作者
Jonhoi Smith,Melvin Field,Kimio Sugaya
出处
期刊:Genes
[Multidisciplinary Digital Publishing Institute]
日期:2023-06-16
卷期号:14 (6): 1276-1276
被引量:13
标识
DOI:10.3390/genes14061276
摘要
Glioblastoma (GBM) is an aggressive and incurable primary brain tumor that harbors therapy-resistant cancer stem cells (CSCs). Due to the limited effectiveness of conventional chemotherapies and radiation treatments against CSCs, there is a critical need for the development of innovative therapeutic approaches. Our previous research revealed the significant expression of embryonic stemness genes, NANOG and OCT4, in CSCs, suggesting their role in enhancing cancer-specific stemness and drug resistance. In our current study, we employed RNA interference (RNAi) to suppress the expression of these genes and observed an increased susceptibility of CSCs to the anticancer drug, temozolomide (TMZ). Suppression of NANOG expression induced cell cycle arrest in CSCs, specifically in the G0 phase, and it concomitantly decreased the expression of PDK1. Since PDK1 activates the PI3K/AKT pathway to promote cell proliferation and survival, our findings suggest that NANOG contributes to chemotherapy resistance in CSCs through PI3K/AKT pathway activation. Therefore, the combination of TMZ treatment with RNAi targeting NANOG holds promise as a therapeutic strategy for GBM.
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