车站3
下调和上调
癌症研究
癌细胞
转录因子
细胞毒性T细胞
生物
化学
细胞生物学
癌症
信号转导
基因
体外
生物化学
遗传学
作者
Bocheng Wu,Benny Payero,Sydney Taylor,Adegboyega K. Oyelere
出处
期刊:Future Medicinal Chemistry
[Newlands Press Ltd]
日期:2021-06-28
卷期号:13 (15): 1253-1269
被引量:5
标识
DOI:10.4155/fmc-2021-0088
摘要
Background: STAT3 is a pro-oncogenic transcription factor. Pyrimethamine (PYM) is a STAT3 inhibitor that suppresses the proliferation of some cancer cells through downregulation of STAT3 target proteins. Methodology & Results: We have used structure-based tools to design novel PYM-based compounds. Intracellular target validation studies revealed that representative compounds 11b-d and 15a downregulate STAT3 downstream proteins and inhibit STAT3 DNA binding domain (DBD). Relative to PYM, a cohort of these compounds are >100-fold more cytotoxic to cancer cells with constitutively active (high pSTAT3) and basal (low pSTAT3) STAT3 signaling, suggesting that STAT3 DBD inhibition is deleterious to the proliferation of cancer cells with low and high pSTAT3 levels. Conclusion: These are promising leads for further preclinical evaluation as therapeutic agents for STAT3-dependent cancers.
科研通智能强力驱动
Strongly Powered by AbleSci AI