Inhibitory Effect of 4-Aryl 2-Substituted Aniline-thiazole Analogs on Growth of Human Prostate Cancer LNCap Cells
作者:Seung-Hwa Baek、Nak-Jeong Kim、Seong-Hwan Kim、Kwang-Hwa Park、Kyung-Chae Jeong、Bae-Keun Park、Nam-Sook Kang
DOI:10.5012/bkcs.2012.33.1.111
日期:2012.1.20
Androgen receptor (AR) is ligand-inducible nuclear hormone receptor which has been focused on key molecular target in growth and progression of prostate cancer. We synthesized a series of 4-aryl 2-substituted aniline-thiazole analogs and evaluated their anti-cancer activity in AR-dependent human prostate cancer LNCap cells. Among them, the compound 6 inhibited the tumor growth in LNCap-inoculated xenograft model.
雄激素受体(AR)是一种配体诱导的核激素受体,已成为前列腺癌生长和进展的关键分子靶点。我们合成了一系列4-芳基-2取代的苯胺-噻唑类似物,并评估了它们在AR依赖的人前列腺癌LNCap细胞中的抗癌活性。在这些化合物中,化合物6抑制了LNCap移植模型中的肿瘤生长。