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余甘子对艾氏腹水癌和人癌细胞系的抗肿瘤及细胞毒性作用。

Antitumor and cytotoxic effects of Phyllanthus polyphyllus on Ehrlich ascites carcinoma and human cancer cell lines.

作者信息

Rajkapoor Balasubramanian, Sankari Marimuthu, Sumithra Mohan, Anbu Jayaraman, Harikrishnan Narayanaswamy, Gobinath Manavalan, Suba Venkatesan, Balaji Ramachandran

机构信息

Department of Pharmacology, Vel's College of Pharmacy, Velan Nagar, Pallavaram, Chennai 600 117, India.

出版信息

Biosci Biotechnol Biochem. 2007 Sep;71(9):2177-83. doi: 10.1271/bbb.70149. Epub 2007 Sep 7.

Abstract

To evaluate the antitumor and cytotoxic activity of methanol extract of Phyllanthus polyphyllus (MPP) in mice and human cancer cell lines, the antitumor activity of MPP was evaluated against an Ehrlich ascites carcinoma (EAC) tumor model. The activity was assessed using survival time, hematological studies, lipid peroxidation (LPO), antioxidant enzymes such as superoxide dismutase (SOD), catalase, glutathione peroxidase (GPx), glutathione S-transferase (GST), solid tumor mass, and short-term in vitro cytotoxicity. The cytotoxic activity of MPP was evaluated using human breast cancer (MCF7), colon cancer (HT29), and liver cancer (HepG2) cell lines Oral administration of MPP (200 and 300 mg/kg) increased the survival time and significantly reduced the solid tumor volume in a dose-dependent manner. Hematological parameters, protein, and packed cellular volume (PCV), which were altered by tumor inoculation, were restored. MPP significantly decreased the levels of LPO, GPx, GST, and significantly increased the levels of SOD and CAT. In a cytotoxicity study against human cancer cell lines, MPP was found to have IC50 values of 27, 42 and 38 microg/ml on MCF-7, HT-29, and HepG2 cells respectively. MPP possessed significant antitumor and cytotoxic activity on EAC and human cancer cell lines.

摘要

为评估多叶叶下珠甲醇提取物(MPP)对小鼠和人癌细胞系的抗肿瘤及细胞毒性活性,针对艾氏腹水癌(EAC)肿瘤模型评估了MPP的抗肿瘤活性。使用生存时间、血液学研究、脂质过氧化(LPO)、抗氧化酶如超氧化物歧化酶(SOD)、过氧化氢酶、谷胱甘肽过氧化物酶(GPx)、谷胱甘肽S-转移酶(GST)、实体瘤块以及短期体外细胞毒性来评估该活性。使用人乳腺癌(MCF7)、结肠癌(HT29)和肝癌(HepG2)细胞系评估了MPP的细胞毒性活性。口服MPP(200和300 mg/kg)可延长生存时间,并以剂量依赖方式显著减小实体瘤体积。因肿瘤接种而改变的血液学参数、蛋白质和红细胞压积(PCV)得以恢复。MPP显著降低LPO、GPx、GST的水平,并显著提高SOD和CAT的水平。在针对人癌细胞系的细胞毒性研究中,发现MPP对MCF-7、HT-29和HepG2细胞的IC50值分别为27、42和38 μg/ml。MPP对EAC和人癌细胞系具有显著的抗肿瘤及细胞毒性活性。

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