Department of Radiation Oncology, Stanford University, Stanford, California.
Department of Neurology, Stanford University, Stanford, California.
Clin Cancer Res. 2017 Jul 1;23(13):3241-3250. doi: 10.1158/1078-0432.CCR-16-3122. Epub 2017 Mar 24.
Cancer therapy has developed around the concept of killing, or stopping the growth of, the cancer cells. Molecularly targeted therapy is the modern expression of this paradigm. Increasingly, however, the realization that the cancer has co-opted the normal cells of the stroma for its own survival has led to the concept that the tumor microenvironment (TME) could be targeted for effective therapy. In this review, we outline the importance of tumor-associated macrophages (TAM), a major component of the TME, in the response of tumors to cancer therapy. We discuss the normal role of macrophages in wound healing, the major phenotypes of TAMs, and their role in blunting the efficacy of cancer treatment by radiation and anticancer drugs, both by promoting tumor angiogenesis and by suppressing antitumor immunity. Finally, we review the many preclinical studies that have shown that the response of tumors to irradiation and anticancer drugs can be improved, sometimes markedly so, by depleting TAMs from tumors or by suppressing their polarization from an M1 to an M2 phenotype. The data clearly support the validity of clinical testing of combining targeting TAMs with conventional therapy. .
癌症治疗的发展围绕着杀死或阻止癌细胞生长的概念。分子靶向治疗是这一范式的现代表达。然而,越来越多的人意识到,癌症已经为了自身的生存而利用了基质中的正常细胞,这导致了一个概念,即肿瘤微环境(TME)可以成为有效的治疗靶点。在这篇综述中,我们概述了肿瘤相关巨噬细胞(TAM)在肿瘤对癌症治疗的反应中的重要性,TAM 是 TME 的主要组成部分。我们讨论了巨噬细胞在伤口愈合中的正常作用、TAM 的主要表型,以及它们通过促进肿瘤血管生成和抑制抗肿瘤免疫来削弱放疗和抗癌药物疗效的作用。最后,我们回顾了许多临床前研究,这些研究表明,通过从肿瘤中耗尽 TAM 或抑制其从 M1 向 M2 表型的极化,可以改善肿瘤对放疗和抗癌药物的反应,有时改善效果非常显著。这些数据清楚地支持了将靶向 TAM 与传统治疗相结合进行临床测试的有效性。