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Anti-cancer effect of N-(3,5-bis(trifluoromethyl)phenyl)-5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-carboxamide, a novel synthetic compound.

作者信息

Kwon Sun Mi, Jung Yu Yeon, Hwang Chul Ju, Park Mi Hee, Yoon Na Young, Kim Tae Myung, Yu Ji Myung, Kim Dae Hwan, Seo Doo Won, Youn Hyu Seok, Seo Hyun Ok, Chung In Sung, Han Sang Bae, Hwang Bang Yeon, Yoo Hwan-Soo, Jung Jae-Kyung, Lee Heesoon, Hong Jin Tae

机构信息

College of Pharmacy and Medical Research Center, Chungbuk National University, Chungbuk, Korea.

College of Veterinary Medicine, Chungbuk National University, Chungbuk, Korea.

出版信息

Mol Carcinog. 2016 May;55(5):659-70. doi: 10.1002/mc.22311. Epub 2015 Apr 11.

Abstract

Naphthofuran compounds have been known to regulate HNF 4α which is associated with proliferation, progression and metastasis of HCC. In this study, we investigated whether N-(3,5-bis(trifluoromethyl)phenyl)-5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-carboxamide (NHDC), a novel synthetic naphthofuran compound inhibits liver tumor growth through activation of HNF 4α. Treatment with different concentrations (1-10.8 µM) of NHDC for various periods (0-72 h) inhibited liver cancer cells (HepG2, Hep3B) growth as well as colony formation followed by induction of apoptosis in a concentration dependent manner. NHDC also induced expression of the apoptosis regulating genes as well as inhibiting the action of STAT3. These inhibitory effects were associated with enhancement of expression and DNA binding activity of HNF 4α. In vivo study confirmed that liver tumor growth was prevented with NHDC (5 mg/kg), and its effect was also related with inhibition of STAT3 pathway through enhancement of expression and DNA binding activity of HNF 4α. Moreover, siRNA of HNF 4α abolished NHDC-induced cell growth inhibition as well as DNA binding activity and phosphorylation of STAT3. Pull down assay docking prediction analysis proved that NHDC directly binds to hydrophobic fatty acid ligand binding site of HNF 4α. A novel naphthofuran compound, NHDC inhibited liver tumor growth by inactivating of STAT3 through direct biding to HNF 4α.

摘要

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