替莫唑胺
胶质瘤
小干扰RNA
下调和上调
基因沉默
热休克蛋白90
细胞凋亡
RNA干扰
癌症研究
细胞周期
医学
细胞培养
癌症
药理学
生物
转染
核糖核酸
内科学
热休克蛋白
生物化学
基因
遗传学
作者
Nichola Cruickshanks,Leroy Shervington,Rahima Patel,Chinmay Munje,Dipti Thakkar,Amal Shervington
标识
DOI:10.3109/07357901003630967
摘要
Hsp90alpha's vital role in cell cycle progression and apoptosis together with its presence in gliomas and absence in normal tissue, make it a credible target for cancer therapy. Three sets of dsRNA oligos designed to align different regions of the hsp90alpha sequence were used to downregulate hsp90alpha. SiRNA 1, 2, and 3 resulted in significant levels of silencing of hsp90alpha after 48 hr treatment (p < .0001). Concurrent treatment of the glioma cell line U87-MG with siRNA 1 and temozolomide (TMZ) resulted in a 13-fold reduction in the dose of TMZ required to achieve a similar effect if TMZ was used alone.
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