激酶
结直肠癌
细胞凋亡
细胞培养
癌症研究
体外
细胞生长
调节器
生长抑制
癌细胞
活力测定
化学
癌症
生物
分子生物学
基因
生物化学
遗传学
作者
SEUNG HYEONG LEE,SU AH KIM,SU JIN PARK,MI YOUNG LEE,Ho Won Seo,GULDANA ISSABAYEVA,Ji Young Hyun,SEONG JUN PARK,Hwan Jung Lim,Woo Dae Jang,Jeong Hyun Lee,Byung Ho Lee,Kwang‐Seok Oh
出处
期刊:Anticancer Research
[International Institute of Anticancer Research (IIAR) Conferences 1997. Athens, Greece. Abstracts]
日期:2024-06-26
卷期号:44 (7): 2909-2919
标识
DOI:10.21873/anticanres.17103
摘要
NUAK family kinase 2 (NUAK2) is a promising target for cancer therapeutics due to its reported role in protein phosphorylation, a critical process in cancer cell survival, proliferation, invasion, and senescence. This study aimed to identify novel inhibitors that disrupt NUAK2 activity. We have already identified two KRICT Hippo kinase inhibitor (KHKI) compounds, such as KHKI-01128 and KHKI-01215. Our aim was to evaluate the impact of KHKI-01128 and KHKI-01215 on NUAK2 activity and elucidate its mechanism in colorectal cancer cells.
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