Department of Biological Sciences, College of Biological Science and Biotechnology, Cancer and Metabolism Institute, Konkuk University, Seoul 143-701, Republic of Korea.
Department of Applied Chemistry, Dongduk Women's University, Seoul 136-714, Republic of Korea.
Cancer Lett. 2014 Nov 28;354(2):348-54. doi: 10.1016/j.canlet.2014.08.041. Epub 2014 Sep 1.
Methoxylated chalcones exert antitumor activities. In the present study, we characterized the cytotoxicity of methylated chalcone derivatives against human colon cancer cells. We synthesized a group of methoxychalcones and explored the molecular mechanisms underlying inhibition of tumor growth by these materials. A new synthetic methoxychalcone, 2'-hydroxy-2,4,6-trimethoxy-5',6'-naphthochalcone (named HMNC-74), most effectively inhibited the clonogenicity of SW620 colon cancer cells. Mechanistically, HMNC-74 triggered cell cycle arrest at G2/M phase, followed by an increase in apoptotic cell death. Our results indicate that the cytotoxicity of the novel compound HMNC-74 involves the disruption of microtubular networks.
甲氧基查耳酮具有抗肿瘤活性。在本研究中,我们对甲氧基查耳酮衍生物对人结肠癌细胞的细胞毒性进行了表征。我们合成了一组甲氧基查耳酮,并探讨了这些物质抑制肿瘤生长的分子机制。一种新的合成甲氧基查耳酮,2'-羟基-2,4,6-三甲氧基-5',6'-萘并查耳酮(命名为 HMNC-74),最有效地抑制了 SW620 结肠癌细胞的集落形成能力。从机制上讲,HMNC-74 诱导细胞周期停滞在 G2/M 期,随后凋亡细胞死亡增加。我们的结果表明,新型化合物 HMNC-74 的细胞毒性涉及微管网络的破坏。