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高迁移率族蛋白B1:一种调控肿瘤进展与免疫的双功能信号分子

HMGB1: a two-headed signal regulating tumor progression and immunity.

作者信息

Campana Lara, Bosurgi Lidia, Rovere-Querini Patrizia

机构信息

Laboratory of Clinical Immunology, San Raffaele Scientific Institute, DIBIT 3A1, Via Olgettina 58, 20132 Milano, Italy.

出版信息

Curr Opin Immunol. 2008 Oct;20(5):518-23. doi: 10.1016/j.coi.2008.04.012. Epub 2008 Jul 1.

Abstract

Cells of the innate immune system sense tissue damage recognizing in the extracellular environment bona fide intracellular moieties, like high mobility group box 1 (HMGB1). In the case of tumors, HMGB1 recognition has a paradoxical dual effect: it promotes tumor neoangiogenesis and triggers protective anti-neoplastic T-cell responses. Recent advances in the study of HMGB1 have identified candidate molecular mechanisms underlying these apparently contrasting outcomes. A surprising role for innate receptors, including toll like receptor 4 (TLR4), in the response to conventional cancer radio and chemotherapy has also recently emerged, providing new insight into the mechanisms by which these treatments actually work.

摘要

先天性免疫系统的细胞通过识别细胞外环境中真实存在的细胞内成分,如高迁移率族蛋白B1(HMGB1),来感知组织损伤。在肿瘤情况下,HMGB1的识别具有矛盾的双重作用:它促进肿瘤新生血管生成并触发保护性抗肿瘤T细胞反应。HMGB1研究的最新进展已经确定了这些明显相反结果背后的候选分子机制。包括Toll样受体4(TLR4)在内的先天性受体在对传统癌症放疗和化疗的反应中的惊人作用最近也已显现,这为这些治疗实际起作用的机制提供了新的见解。

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