| Literature DB >> 29760237 |
Jiamiao Hu1,2, Si Kee Tan3, Michelle Gek Liang Lim3, Shie Hong Chang1, Guimei Cui1, Shanshan Liu1,4, Kamesh Narasimhan3, Siu Yee New5, Xuecong Wang6, Congling Chen6, Harapriya Chakravarty1, Prasanna R Kolatkar3, Kin Yip Tam1, Qian Lu4, Xiaodi Su5, Ralf Jauch3,6, Edwin Cheung7,3.
Abstract
AP-2 gamma (AP-2γ) is a transcription factor that plays pivotal roles in breast cancer biology. To search for small molecule inhibitors of AP-2γ, we performed a high-throughput fluorescence anisotropy screen and identified a polyoxometalate compound with Wells-Dawson structure K6[P2Mo18O62] (Dawson-POM) that blocks the DNA-binding activity of AP-2γ. We showed that this blocking activity is due to the direct binding of Dawson-POM to AP-2γ. We also provided evidence to show that Dawson-POM decreases AP-2γ-dependent transcription similar to silencing the gene. Finally, we demonstrated that Dawson-POM contains anti-proliferative and pro-apoptotic effects in breast cancer cells. In summary, we identified the first small molecule inhibitor of AP-2γ and showed Dawson-POM-mediated inhibition of AP-2γ as a potential avenue for cancer therapy.Entities:
Keywords: AP-2γ; breast cancer; fluorescent anisotropic; polyoxometalate
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Year: 2018 PMID: 29760237 DOI: 10.1042/BCJ20170942
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857