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莱奇酶对癌症细胞的选择性凋亡诱导作用

Cancer-selective induction of apoptosis by leczyme.

作者信息

Tatsuta Takeo, Sugawara Shigeki, Takahashi Kohta, Ogawa Yukiko, Hosono Masahiro, Nitta Kazuo

机构信息

Division of Cell Recognition Study, Institute of Molecular Biomembrane and Glycobiology, Tohoku Pharmaceutical University , Sendai , Japan.

Divisions of Functional Morphology and Microbiology, Department of Pharmacy, Faculty of Pharmaceutical Science, Nagasaki International University , Sasebo , Japan.

出版信息

Front Oncol. 2014 Jun 4;4:139. doi: 10.3389/fonc.2014.00139. eCollection 2014.

Abstract

Sialic acid-binding lectin (SBL) is a multi-functional protein that is isolated from oocytes of Rana catesbeiana. It has both lectin and ribonuclease (enzyme) properties, and therefore is called leczyme. We examined the anti-tumor effects of SBL and discovered that SBL has potential as a new type of anti-cancer drug. SBL causes a cancer-selective induction of apoptosis by multiple signaling pathways whereby RNA is its target. It is suggested that the mitochondrial pathway and endoplasmic reticulum stress-mediated pathway participate in SBL-induced signaling. The synergistic anti-tumor effects with other molecules, such as tumor necrosis factor-related apoptosis ligand and interferon γ, have been reported. In this study, we summarize the effects of SBL and focus on its cancer-selective apoptotic properties. In addition, we present a possible explanation for its cancer specificity.

摘要

唾液酸结合凝集素(SBL)是一种从牛蛙卵母细胞中分离出来的多功能蛋白质。它同时具有凝集素和核糖核酸酶(酶)的特性,因此被称为凝集酶。我们研究了SBL的抗肿瘤作用,发现SBL有潜力成为一种新型抗癌药物。SBL通过多种信号通路导致癌症选择性凋亡诱导,其中RNA是其靶点。提示线粒体途径和内质网应激介导的途径参与了SBL诱导的信号传导。已有报道称其与其他分子,如肿瘤坏死因子相关凋亡配体和干扰素γ具有协同抗肿瘤作用。在本研究中,我们总结了SBL的作用,并着重关注其癌症选择性凋亡特性。此外,我们对其癌症特异性提出了一种可能的解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f82/4044787/b7dc7242f4b4/fonc-04-00139-g001.jpg

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