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原花青素调节中性粒细胞胞外陷阱形成并抑制肝癌细胞的生长和增殖——体内、体外和计算机模拟研究

Proanthocyanidin Regulates NETosis and Inhibits the Growth and Proliferation of Liver Cancer Cells - In Vivo, In Vitro and In Silico Investigation.

作者信息

Wang Chenhui, Xia Wu

机构信息

Department of Pharmaceutical, Brain Hospital of Hunan Province, The Second People's Hospital of Hunan Province, No. 427, Section 3, Furong Middle Road, Changsha, 410007, China.

出版信息

Cell Biochem Biophys. 2025 Mar;83(1):1223-1235. doi: 10.1007/s12013-024-01557-6. Epub 2024 Oct 9.

DOI:10.1007/s12013-024-01557-6
PMID:39382828
Abstract

Liver cancer ranks third in global cancer-related mortality, with about 700,000 deaths recorded yearly, making it one of the most common cancers worldwide. Even though prognoses differ according to the severity of the diseases, many patients now exhibit an increased life cycle since the implementation of chemotherapy. In the current study, we investigated the effect of proanthocyanidin ‒a polyphenol molecule found in many plants‒ on the proliferation and invasion of liver cancer cells. In particular, we determined the effect of proanthocyanidin on the serum levels of four strategic liver cancer target, TNFα, IL-6, cfDNA, and IL-1β. Further molecular insight on the inhibitory mechanism of proanthocyanidin against TNFα, IL-6, and IL-1β was obtained via molecular docking, molecular dynamics simulations and binding free energy calculations. Results showed that proanthocyanidin inhibited the growth of HepG2 and HEP3B cells, and effectively reduced clonogenic survival and invasion potential when compared to control cells. Proanthocyanidin was also found to suppress the expression of Bcl-2 (26 kDa) protein in HepG2 cells, while increasing the expression of Bax (21 kDa). Molecular dynamics (MD) and thermodynamic binding free energy calculations showed that proanthocyanidin maintained stable binding within the active site of target proteins across the entire 100 ns MD simulation period, and its binding affinity outscored respective control molecules.In conclusion, the multifaceted analysis showcased in this study demonstrated promising anti-cancer effect of proanthocyanidin on HepG2 and HEP3B cancer cells, highlighting its potential as a viable liver cancer therapeutic alternative.

摘要

肝癌在全球癌症相关死亡率中排名第三,每年约有70万人死亡,是全球最常见的癌症之一。尽管预后因疾病严重程度而异,但自实施化疗以来,许多患者的生命周期有所延长。在本研究中,我们研究了原花青素(一种在许多植物中发现的多酚分子)对肝癌细胞增殖和侵袭的影响。具体而言,我们确定了原花青素对四种关键肝癌靶点(TNFα、IL-6、cfDNA和IL-1β)血清水平的影响。通过分子对接、分子动力学模拟和结合自由能计算,对原花青素对TNFα、IL-6和IL-1β的抑制机制有了进一步的分子认识。结果表明,与对照细胞相比,原花青素抑制了HepG2和HEP3B细胞的生长,并有效降低了克隆形成存活率和侵袭潜力。还发现原花青素抑制HepG2细胞中Bcl-2(26 kDa)蛋白的表达,同时增加Bax(21 kDa)的表达。分子动力学(MD)和热力学结合自由能计算表明,在整个100 ns的MD模拟期间,原花青素在靶蛋白的活性位点内保持稳定结合,其结合亲和力超过各自的对照分子。总之,本研究中展示的多方面分析表明原花青素对HepG2和HEP3B癌细胞具有有前景的抗癌作用,突出了其作为可行的肝癌治疗替代品的潜力。

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