ULK1
自噬
三阴性乳腺癌
激活剂(遗传学)
生物
癌症研究
细胞生物学
自噬相关蛋白13
激酶
癌症
乳腺癌
细胞凋亡
蛋白激酶A
生物化学
遗传学
基因
细胞周期蛋白依赖激酶2
安普克
作者
Liang Ouyang,Lan Zhang,Leilei Fu,Bo Liu
出处
期刊:Autophagy
[Informa]
日期:2017-02-28
卷期号:13 (4): 777-778
被引量:31
标识
DOI:10.1080/15548627.2017.1283470
摘要
ULK1 (unc-51 like autophagy activating kinase 1) is well known to be required to initiate the macroautophagy/autophagy process, and thus activation of ULK1-modulating autophagy/autophagy-associated cell death (ACD) may be a possible therapeutic strategy in triple negative breast cancer (TNBC). Here, our integrated The Cancer Genome Atlas (TCGA) data set, tissue microarray-based analyses and multiple biologic evaluations together demonstrate a new small-molecule activator of ULK1 for better understanding of how ULK1, the mammalian homolog of yeast Atg1, as a potential drug target can regulate ACD by the ULK complex (ULK1-ATG13-RB1CC1/FIP200-ATG101), as well as other possible ULK1 interactors, including ATF3, RAD21 and CASP3/caspase3 in TNBC. Moreover, such new inspiring findings may help us discover that this activator of ULK1 (LYN-1604) with its anti-tumor activity and ACD-modulating mechanisms can be further exploited as a small-molecule candidate drug for future TNBC therapy.
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