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一种可能的抗癌剂,III型干扰素,可激活细胞死亡途径并产生抗肿瘤作用。

A possible anticancer agent, type III interferon, activates cell death pathways and produces antitumor effects.

作者信息

Tagawa Masatoshi, Kawamura Kiyoko, Li Quanhai, Tada Yuji, Hiroshima Kenzo, Shimada Hideaki

机构信息

Division of Pathology and Cell Therapy, Chiba Cancer Center Research Institute, 666-2 Nitona, Chuo-ku, Chiba 260-8717, Japan.

出版信息

Clin Dev Immunol. 2011;2011:479013. doi: 10.1155/2011/479013. Epub 2011 Oct 16.

Abstract

Recently identified interleukin-28 and -29 belong to a novel type III interferon (IFN) family, which could have distinct biological properties from type I and II IFNs. Type I IFNs, IFN-α/β, have been clinically applied for treating a certain kind of malignancies for over 30 years, but a wide range of the adverse effects hampered the further clinical applications. Type III IFNs, IFN-λs, have similar signaling pathways as IFN-α/β and inhibits proliferation of tumor cells through cell cycle arrest or apoptosis. Restricted patterns of type III IFN receptor expression in contrast to ubiquitously expressed IFN-α/β receptors suggest that type III IFNs have limited cytotoxicity to normal cells and can be a possible anticancer agent. In this paper, we summarize the current knowledge on the IFN-λs-mediated tumor cell death and discuss the functional difference between type I and III IFNs.

摘要

最近发现的白细胞介素-28和-29属于一种新型III型干扰素(IFN)家族,其生物学特性可能与I型和II型干扰素不同。I型干扰素IFN-α/β已临床应用于治疗某些恶性肿瘤30多年,但广泛的不良反应阻碍了其进一步的临床应用。III型干扰素IFN-λs具有与IFN-α/β相似的信号通路,并通过细胞周期停滞或凋亡抑制肿瘤细胞增殖。与普遍表达的IFN-α/β受体相比,III型干扰素受体表达模式受限,这表明III型干扰素对正常细胞的细胞毒性有限,可能是一种潜在的抗癌药物。在本文中,我们总结了目前关于IFN-λs介导的肿瘤细胞死亡的知识,并讨论了I型和III型干扰素之间的功能差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/433f/3195555/b0ebd6ea4914/CDI2011-479013.001.jpg

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