黄酮类化合物在肿瘤发病机制中作为MMP-2和MMP-9调控因子的研究

IF 3.3 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ha Vy Thi Vo, Geewoo Nam Patton, Song Ja Kim, Namdoo Kim, Hyuck Jin Lee
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引用次数: 0

摘要

在过去的几十年里,广泛的研究工作一直致力于发现新的癌症治疗方法。在这种追求中最重要的目标是基质金属蛋白酶(MMPs),这是癌症进展和扩散不可或缺的酶。它们在肿瘤发展和转移中的作用使MMPs成为癌症发病机制的关键参与者,为治疗干预提供了有希望的途径。具体来说,MMP-2和MMP-9在细胞侵袭、血管生成、免疫逃避和转移中的关键作用已成为癌症治疗中有希望的靶点。研究表明,植物源性天然产物可能通过调控MMP活性而成为抗癌药物。在各种植物化学物质中,黄酮类化合物被报道对MMPs具有抑制活性和抗氧化特性,使其成为抗癌分子的候选者。本研究通过研究黄酮类化合物对肿瘤细胞活力和迁移、MMP-2/9的酶活性和细胞表达以及MAPK信号通路的影响,探讨了黄酮类化合物作为抗癌药物的潜力。关于MMP-2/9与选定的黄酮类化合物之间相互作用的对接模拟数据提供了深入了解这些分子抑制MMPs酶活性的潜在机制。部分黄酮类化合物对A549细胞的增殖和迁移具有明显的抑制作用,这可能是其通过抑制MAPK信号通路来减弱MMP活性和表达的结果。这些观察结果表明,黄酮类化合物作为一种天然存在的分子框架,有望开发新的抗癌疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exploring Flavonoids as Regulators of MMP-2 and MMP-9 in Cancer Pathogenesis

Exploring Flavonoids as Regulators of MMP-2 and MMP-9 in Cancer Pathogenesis

Last few decades, extensive research efforts have been dedicated to uncovering novel cancer treatments. Among the most vital targets in this pursuit are matrix metalloproteinases (MMPs), enzymes integral to the progression and spread of cancer. Their role in tumor development and metastasis positions MMPs as key players in cancer pathogenesis, offering promising avenues for therapeutic intervention. Specifically, MMP-2 and MMP-9 have emerged as promising targets in cancer treatment based on their critical roles in cell invasion, angiogenesis, immune evasion, and metastasis. Studies indicate the potential of plant-derived natural products as anticancer agents through the regulation of MMP activity. Among various phytochemicals, flavonoids are reported to exhibit inhibitory activities against MMPs and antioxidant properties that present them as candidates for anticancer molecules. In this study, the potential of flavonoids as anticancer agents was explored by investigating the effects of flavonoids on (i) cancer cell viability and migration, (ii) enzymatic activity and cellular expression of MMP-2/9, and (iii) the MAPK signaling pathway. Docking simulation data regarding the interactions between MMP-2/9 and selected flavonoids provide an in-depth look at the potential mechanisms through which these molecules suppress the enzymatic activities of MMPs. Select flavonoids exhibited notable efficacy in suppressing cell proliferation and migration in A549 cells, which may be a consequence of their ability to attenuate MMP activity and expression through the suppression of the MAPK signaling pathway. These observations demonstrate the prospect of flavonoids as a naturally occurring molecular framework for the development of novel anticancer therapeutics.

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来源期刊
Chemical Biology & Drug Design
Chemical Biology & Drug Design 医学-生化与分子生物学
CiteScore
5.10
自引率
3.30%
发文量
164
审稿时长
4.4 months
期刊介绍: Chemical Biology & Drug Design is a peer-reviewed scientific journal that is dedicated to the advancement of innovative science, technology and medicine with a focus on the multidisciplinary fields of chemical biology and drug design. It is the aim of Chemical Biology & Drug Design to capture significant research and drug discovery that highlights new concepts, insight and new findings within the scope of chemical biology and drug design.
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