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通过 EZH2 抑制克服免疫检查点阻断耐药性。

Overcoming Immune Checkpoint Blockade Resistance via EZH2 Inhibition.

机构信息

Department of Cancer Immunology and Virology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Department of Immunology, Harvard Medical School, Boston, MA 02115, USA.

Epizyme, Inc., Cambridge, MA 02139, USA.

出版信息

Trends Immunol. 2020 Oct;41(10):948-963. doi: 10.1016/j.it.2020.08.010.

Abstract

Recent progress in cancer immunotherapy highlights the power of the immune system to control tumors, although a small patient subset responds to current immunotherapies. Additional approaches to mobilize antitumor immunity are required to overcome primary and acquired resistance to immunotherapy such as immune checkpoint blockade (ICB). Emerging evidence shows that targeting epigenetic elements that promote tumor progression and inhibit immune cell activity can enhance antitumor immunity by reshaping the tumor microenvironment (TME). Here, we review the pleiotropic functions in tumor and immune cells of enhancer of zeste homolog 2 (EZH2), the catalytic subunit of polycomb repressive complex 2 (PRC2), with a focus on EZH2 inhibition as a potentially promising approach to enhance current immunotherapies and improve patient outcomes for certain cancers.

摘要

近年来癌症免疫疗法的进展突显了免疫系统控制肿瘤的能力,尽管目前的免疫疗法仅对一小部分患者有效。需要采取额外的方法来调动抗肿瘤免疫,以克服免疫检查点阻断 (ICB) 等免疫疗法的原发性和获得性耐药。新出现的证据表明,靶向促进肿瘤进展和抑制免疫细胞活性的表观遗传元件可以通过重塑肿瘤微环境 (TME) 来增强抗肿瘤免疫。在这里,我们回顾了增强子结合锌指蛋白 2 (EZH2)——多梳抑制复合物 2 (PRC2) 的催化亚基——在肿瘤和免疫细胞中的多效功能,重点讨论了 EZH2 抑制作为一种增强现有免疫疗法和改善某些癌症患者预后的潜在有前途的方法。

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