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槲寄生中的重组 VAA-I 诱导肝癌 SMMC7721 细胞凋亡。

Recombinant VAA-I from Viscum album induces apoptotic cell death of hepatocellular carcinoma SMMC7721 cells.

机构信息

Department of Hepatobiliary and Pancreatic Surgery, the First Clinical Hospital, Jilin University, Jilin, China.

出版信息

Molecules. 2012 Sep 26;17(10):11435-46. doi: 10.3390/molecules171011435.

Abstract

Researchers have proposed that VAA-I, a specific plant lectin found in Viscum album, has therapeutic effects on cancer and autoimmune diseases. VAA-I has shown some promising treatment results in some types of tumor cell lines, especially SMMC-7721 cells (human hepatocellular carcinoma cells). However, few details are known about the mechanism and process of cell death induced by VAA-I in tumor cells. In this study, the cell morphology results showed that SMMC-7721 cells treated with VAA-I exhibited several features typical of apoptotic cell death, which was confirmed by the Caspase inhibition assay. Fluo-3-acetoxymethyl ester (AM) fluorescence imaging techniques showed that rVAA-I significantly elevated the intracellular calcium level ([Ca2+]i) in SMMC-7721 cells. These findings suggest that apoptosis may play the most important role in SMMC-7721 cell death induced by rVAA-I. Finally, in the SMMC-7721 cells treated with rVAA-I, a series of genes in the p38 mitogen-activated protein kinase (MAPK) signaling pathway were expressed differentially, and further found that PI 3-kinase pathway is involved in rVAA-I signal transduction in SMMC-7721 cells.

摘要

研究人员提出,槲寄生中一种特定的植物凝集素 VAA-I 对癌症和自身免疫性疾病具有治疗作用。VAA-I 在某些类型的肿瘤细胞系中显示出一些有希望的治疗结果,特别是 SMMC-7721 细胞(人肝癌细胞)。然而,关于 VAA-I 在肿瘤细胞中诱导细胞死亡的机制和过程知之甚少。在这项研究中,细胞形态学结果表明,用 VAA-I 处理的 SMMC-7721 细胞表现出几种典型的凋亡细胞死亡特征,这通过 Caspase 抑制测定得到了证实。Fluo-3-乙酰氧甲酯(AM)荧光成像技术显示,rVAA-I 显著升高了 SMMC-7721 细胞中的细胞内钙离子水平([Ca2+]i)。这些发现表明,凋亡可能在 rVAA-I 诱导的 SMMC-7721 细胞死亡中起最重要的作用。最后,在用 rVAA-I 处理的 SMMC-7721 细胞中,p38 丝裂原活化蛋白激酶(MAPK)信号通路中的一系列基因表达差异,进一步发现 PI 3-激酶通路参与了 rVAA-I 在 SMMC-7721 细胞中的信号转导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29be/6268905/117395875399/molecules-17-11435-g004.jpg

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