Yin Kai, Xia Xueli, Rui Ke, Wang Tingting, Wang Shengjun
Department of General Surgery, Affiliated Hospital of Jiangsu University, Zhenjiang, China.
Department of Immunology, Jiangsu Key Laboratory of Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, China.
Front Oncol. 2020 Dec 15;10:610104. doi: 10.3389/fonc.2020.610104. eCollection 2020.
Colorectal cancer (CRC) remains a devastating human malignancy with poor prognosis. Of the various factors, immune evasion mechanisms play pivotal roles in CRC progression and impede the effects of cancer therapy. Myeloid-derived suppressor cells (MDSCs) constitute an immature population of myeloid cells that are typical during tumor progression. These cells have the ability to induce strong immunosuppressive effects within the tumor microenvironment (TME) and promote CRC development. Indeed, MDSCs have been shown to accumulate in both tumor-bearing mice and CRC patients, and may therefore become an obstacle for cancer immunotherapy. Consequently, numerous studies have focused on the characterization of MDSCs and their immunosuppressive capacity, as well as developing novel approaches to suppress MDSCs function with different approaches. Current therapeutic strategies that target MDSCs in CRC include inhibition of their recruitment and alteration of their function, alone or in combination with other therapies including chemotherapy, radiotherapy and immunotherapy. Herein, we summarize the recent roles and mechanisms of MDSCs in CRC progression. In addition, a brief review of MDSC-targeting approaches for potential CRC therapy is presented.
结直肠癌(CRC)仍然是一种预后较差的毁灭性人类恶性肿瘤。在各种因素中,免疫逃逸机制在CRC进展中起关键作用,并阻碍癌症治疗的效果。髓系来源的抑制细胞(MDSCs)构成了一群未成熟的髓系细胞,在肿瘤进展过程中很典型。这些细胞有能力在肿瘤微环境(TME)中诱导强烈的免疫抑制作用,并促进CRC的发展。事实上,MDSCs已被证明在荷瘤小鼠和CRC患者中都会积累,因此可能成为癌症免疫治疗的障碍。因此,许多研究集中在MDSCs的特征及其免疫抑制能力上,以及开发用不同方法抑制MDSCs功能的新方法。目前在CRC中针对MDSCs的治疗策略包括抑制其募集和改变其功能,单独或与包括化疗、放疗和免疫治疗在内的其他疗法联合使用。在此,我们总结了MDSCs在CRC进展中的最新作用和机制。此外,还简要综述了针对潜在CRC治疗的靶向MDSCs的方法。