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癌症免疫逃逸的机制与克服策略的发展。

The mechanisms of cancer immunoescape and development of overcoming strategies.

机构信息

Division of Cellular Signaling, Institute for Advanced Medical Research, 35 Shinanomachi, Shinjuku, Tokyo, Japan.

Department of Obstetrics and Gynecology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, Tokyo, Japan.

出版信息

Int J Hematol. 2011 Mar;93(3):294-300. doi: 10.1007/s12185-011-0799-6. Epub 2011 Mar 5.

Abstract

Cancer-induced immunosuppression is a major problem as it reduces the anti-tumor effects of immunotherapies. In cancer tissues, cancer cells, immune cells, and other stromal cells interact and create an immunosuppressive microenvironment through a variety of immunosuppressive factors. Some cancer subpopulations such as cancer cells undergoing epithelial-mesenchymal transition and cancer stem-like cells have immunosuppressive and immunoresistant properties. The production of immunosuppressive factors by cancer cells is mechanistically attributed to oncogenic signals frequently activated in cancer cells, including the STAT3, MAPK, NF-κB, and Wnt/β-catenin signals, which are upstream events leading to immunosuppressive cascades. Moreover, some of these signals are also activated in immunosuppressive immune cells stimulated by cancer-derived factors and contribute to their immunosuppressive activities. Therefore, targeting these signals both in cancer cells and immunosuppressive immune cells may result in the restoration of immunocompetence in cancer patients and improve current immunotherapy.

摘要

癌症引起的免疫抑制是一个主要问题,因为它降低了免疫疗法的抗肿瘤作用。在癌症组织中,癌细胞、免疫细胞和其他基质细胞相互作用,并通过多种免疫抑制因子产生免疫抑制微环境。一些癌症亚群,如经历上皮-间充质转化的癌细胞和癌症干细胞样细胞,具有免疫抑制和免疫抵抗特性。癌细胞产生免疫抑制因子的机制归因于经常在癌细胞中激活的致癌信号,包括 STAT3、MAPK、NF-κB 和 Wnt/β-catenin 信号,这些信号是导致免疫抑制级联反应的上游事件。此外,一些这些信号也在癌症衍生因子刺激的免疫抑制性免疫细胞中被激活,并有助于它们的免疫抑制活性。因此,靶向这些信号在癌细胞和免疫抑制性免疫细胞中可能会恢复癌症患者的免疫能力,并改善当前的免疫疗法。

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