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肿瘤基质作为癌症治疗的靶点。

Tumor stroma as a target in cancer.

作者信息

Ahmed F, Steele J C, Herbert J M J, Steven N M, Bicknell R

机构信息

Cancer Research UK Angiogenesis Group, Institute for Biomedical Research, University of Birmingham Medical School, Edgbaston, Birmingham, B15 2TT, UK,

出版信息

Curr Cancer Drug Targets. 2008 Sep;8(6):447-53. doi: 10.2174/156800908785699360.

Abstract

Solid tumors are composed of the malignant cell itself (most commonly a carcinoma) and supporting cells that comprise the stroma. Significant stromal components include the extracellular matrix, supporting fibroblasts, vessels comprised of endothelium, pericytes and in some cases vascular smooth muscle, lymphatics and usually a major leukocyte infiltration. Indeed, macrophages may constitute up to 50% of the viable cells within the tumor. For many years, researchers have concentrated almost exclusively on the malignant carcinoma and looked for ways to either selectively kill or restrict its growth. In recent years the frustrating lack of advances in cytotoxic cancer therapy provoked a search for more novel strategies and foremost amongst these were anti-angiogenesis and vascular targeting. The purpose of this article is to illustrate how the stroma is now being pursued as an anti-cancer target. The article will briefly touch on anti-angiogenics that are now entering the clinic but concentrate on recent studies looking at vascular disrupting agents, stromal tumor fibroblasts and macrophages. Target identification is illustrated by the search for tumor endothelial markers. Finally, we draw attention to efforts to develop a cancer vaccine. The genetic instability and variation found in carcinoma cells made vaccination in the past a near impossibility. In contrast, genetically stable tumor endothelium with its unique accessibility to blood borne agents, together with recent advances in immunotherapy means that the possibility of a cancer vaccine now takes on a reality not previously recognised.

摘要

实体瘤由恶性细胞本身(最常见的是癌)和构成基质的支持细胞组成。重要的基质成分包括细胞外基质、支持性成纤维细胞、由内皮细胞、周细胞以及某些情况下的血管平滑肌组成的血管、淋巴管,通常还有大量白细胞浸润。实际上,巨噬细胞可能占肿瘤内活细胞的50%。多年来,研究人员几乎只专注于恶性癌,并寻找选择性杀死或限制其生长的方法。近年来,细胞毒性癌症治疗令人沮丧地缺乏进展,促使人们寻找更新颖的策略,其中最主要的是抗血管生成和血管靶向。本文的目的是说明现在如何将基质作为抗癌靶点。本文将简要提及目前正在进入临床的抗血管生成药物,但重点关注近期关于血管破坏剂、基质肿瘤成纤维细胞和巨噬细胞的研究。通过寻找肿瘤内皮标志物来说明靶点识别。最后,我们提请注意开发癌症疫苗的努力。癌细胞中发现的基因不稳定性和变异性使得过去进行疫苗接种几乎不可能。相比之下,基因稳定的肿瘤内皮细胞对血源性病原体具有独特的可及性,再加上免疫治疗的最新进展,意味着癌症疫苗的可能性现在成为了一个以前未被认识到的现实。

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