Suppr超能文献

一种新型合成的 2'-羟基-2,4,6-三甲氧基-5',6'-萘并查尔酮通过破坏人结肠癌细胞的微管网络诱导 G2/M 细胞周期停滞和细胞凋亡。

A new synthetic 2'-hydroxy-2,4,6-trimethoxy-5',6'-naphthochalcone induces G2/M cell cycle arrest and apoptosis by disrupting the microtubular network of human colon cancer cells.

机构信息

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.

出版信息

Cancer Lett. 2014 Nov 28;354(2):348-54. doi: 10.1016/j.canlet.2014.08.041. Epub 2014 Sep 1.

Abstract

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.

摘要

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。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验