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研究糙皮侧耳多糖对艾氏腹水癌细胞 G0/G1 期细胞周期阻滞和凋亡的抗癌作用。

Investigating the Anticancer Effects of Pleurotus ostreatus Polysaccharide on G0/G1 Cell Cycle Arrest and Apoptosis in Ehrlich Ascites Carcinoma Cells.

机构信息

Institute of Biological Sciences, Rajshahi University, Rajshahi-6205, Bangladesh.

Department of Anaesthesiology and Critical Care, Tallaght University Hospital, Dublin, Ireland.

出版信息

Chem Biodivers. 2024 Sep;21(9):e202400897. doi: 10.1002/cbdv.202400897. Epub 2024 Aug 26.

Abstract

Cancer is one of the leading causes of mortality worldwide. Despite the advancement of cancer treatment by various means including surgery, chemotherapy etc, cancer is still a challenging disease to manage. This study was undertaken to investigate extraction, purification, structural elucidation, and the potential anti-cancer effects of Pleurotus ostreatus polysaccharide (POP). The anti-cancer activities were performed on the Ehrlich Ascites Carcinoma Cell Line. The results demonstrated that the MW of POP was154649.8 Da with homopolysaccharide composed of D-glucose units, featuring (1→6)-α-D-Glcp backbone with O-6 branches and T-α-D-Glcp terminations. and the yield was 6.27 %. The antitumor activity assessment demonstrated significant cytotoxicity of POP against Ehrlich Ascites Carcinoma (EAC) cells, with an IC of 121.801 μg mL, supported by LDH release analysis. POP inhibited cell migration, invasion, and colony formation, indicating its potential as an anti-cancer agent. POP elicited the apoptotic activity with the upregulation of Caspase-9 and Bax, and downregulation of Bcl-2. The DNA fragmentation assay further confirmed apoptosis-mediated DNA degradations. Additionally, POP-induced cell cycle arrest at the G0/G1 phase, by altering the expression of p53, Cyclin D, and Cdk4 proteins. So, Pleurotus ostreatus polysaccharide (POP) showed significant cytotoxicity on Ehrlich Ascites Carcinoma cells, indicating potential as an anti-cancer agent.

摘要

癌症是全球主要的死亡原因之一。尽管通过手术、化疗等各种手段推进了癌症治疗,但癌症仍然是一种难以治疗的疾病。本研究旨在探讨糙皮侧耳多糖(POP)的提取、纯化、结构解析及潜在的抗癌作用。采用艾氏腹水癌细胞系进行抗癌活性研究。结果表明,POP 的 MW 为 154649.8 Da,由 D-葡萄糖单元组成的均多糖,具有(1→6)-α-D-Glcp 主链和 O-6 支链以及 T-α-D-Glcp 末端,产率为 6.27%。肿瘤细胞活性评估表明,POP 对艾氏腹水癌细胞(EAC)具有显著的细胞毒性,IC 为 121.801 μg mL,这一结果得到 LDH 释放分析的支持。POP 抑制细胞迁移、侵袭和集落形成,表明其具有作为抗癌剂的潜力。POP 通过上调 Caspase-9 和 Bax 并下调 Bcl-2 诱导细胞凋亡活性。DNA 片段化分析进一步证实了凋亡介导的 DNA 降解。此外,POP 通过改变 p53、Cyclin D 和 Cdk4 蛋白的表达,将细胞周期阻滞在 G0/G1 期。因此,糙皮侧耳多糖(POP)对艾氏腹水癌细胞具有显著的细胞毒性,表明其具有作为抗癌剂的潜力。

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