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首页> 外文期刊>Bioorganic and medicinal chemistry >Polyphenols bearing cinnamaldehyde scaffold showing cell growth inhibitory effects on the cisplatin-resistant A2780/Cis ovarian cancer cells
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Polyphenols bearing cinnamaldehyde scaffold showing cell growth inhibitory effects on the cisplatin-resistant A2780/Cis ovarian cancer cells

机译:含有肉桂醛支架的多酚,显示细胞生长抑制对顺铂A2780 / CIS卵巢癌细胞的影响

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摘要

Ovarian carcinoma remains the most lethal among gynecological cancers. Chemoresistance is a clinical problem that severely limits treatment success. To identify potent anticancer agents against the cisplatin-resistant human ovarian cancer cell line A2780/Cis, 26 polyphenols bearing a cinnamaldehyde scaffold were synthesized. Structural differences in their inhibitory effect on clonogenicity of A2780/Cis cells were elucidated using comparative molecular field analysis and comparative molecular similarity indices analysis. Structural conditions required for increased inhibitory activity can be derived based on the analysis of their contour maps. The two most active compounds (16 and 19) were selected and further characterized their biological activities. We found that compounds 16 and 19 trigger cell cycle arrest at the G2/M phase and apoptotic cell death in cisplatin-resistant A2780/Cis human ovarian cancer cells. The molecular mechanism of compound 16 was elucidated using in vitro aurora A kinase assay, and the binding mode between the compound 16 and aurora A kinase was interpreted using in silico docking experiments. The findings obtained here may help us develop novel plant-derived polyphenols used for potent chemotherapeutic agents. In conclusion, compounds 16 and 19 could be used as promising lead compounds for the development of novel anticancer therapies in the treatment of cisplatin-resistant ovarian cancers.
机译:卵巢癌仍然是妇科癌症中最致命的癌症。化学抑制是一种严重限制治疗成功的临床问题。为了鉴定抗顺铂抗性的人卵巢癌细胞系A2780 / CIS的有效抗癌剂,合成了26种含有肉桂醛支架的多酚。使用比较分子场分析和比较分子相似索引分析阐明了对A2780 / CIS细胞克隆性的抑制性的结构差异。可以基于对轮廓图的分析来导出增加的抑制活动所需的结构条件。选择两个最活跃的化合物(16和19),并进一步表征其生物活性。我们发现,在顺铂抗性A2780 / CIS人卵巢癌细胞中,化合物16和19触发G2 / M相和凋亡细胞死亡的细胞周期停滞。使用体外极光激酶测定法阐明化合物16的分子机制,并且在硅对接实验中使用化合物16和极光之间的结合模式解释。这里获得的发现可以帮助我们开发用于有效化学治疗剂的新型植物衍生的多酚。总之,化合物16和19可用作有前途的铅化合物,用于开发新型抗癌疗法治疗顺铂抗性卵巢癌。

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  • 来源
    《Bioorganic and medicinal chemistry 》 |2014年第6期| 共12页
  • 作者单位

    Department of Biological Sciences Konkuk University Seoul 143-701 South Korea;

    Division of Bioscience and Biotechnology BMIC Konkuk University Hwayang-Dong 1 Kwangjin-Gu;

    Division of Bioscience and Biotechnology BMIC Konkuk University Hwayang-Dong 1 Kwangjin-Gu;

    Division of Bioscience and Biotechnology BMIC Konkuk University Hwayang-Dong 1 Kwangjin-Gu;

    Division of Bioscience and Biotechnology BMIC Konkuk University Hwayang-Dong 1 Kwangjin-Gu;

    Division of Bioscience and Biotechnology BMIC Konkuk University Hwayang-Dong 1 Kwangjin-Gu;

    Division of Bioscience and Biotechnology BMIC Konkuk University Hwayang-Dong 1 Kwangjin-Gu;

    Division of Bioscience and Biotechnology BMIC Konkuk University Hwayang-Dong 1 Kwangjin-Gu;

    Department of Applied Chemistry Dongduk Women's University Seoul 136-714 South Korea;

    Department of Biological Sciences Konkuk University Seoul 143-701 South Korea;

    Division of Bioscience and Biotechnology BMIC Konkuk University Hwayang-Dong 1 Kwangjin-Gu;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药学 ;
  • 关键词

    Aurora A; Chalcone; Cinnamaldehyde; Clonogenicity; Ovarian cancer; QSAR;

    机译:Aurora a;chalcone;肉桂醛;克隆根;卵巢癌;qsar;

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