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免疫原性细胞死亡在结直肠癌预防和治疗中的作用。

Immunogenic cell death in colon cancer prevention and therapy.

机构信息

Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.

UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania.

出版信息

Mol Carcinog. 2020 Jul;59(7):783-793. doi: 10.1002/mc.23183. Epub 2020 Mar 25.

Abstract

Colorectal cancer (CRC) is a leading cause of cancer-related death worldwide. The colonic mucosa constitutes a critical barrier and a major site of immune regulation. The immune system plays important roles in cancer development and treatment, and immune activation caused by chronic infection or inflammation is well-known to increase cancer risk. During tumor development, neoplastic cells continuously interact with and shape the tumor microenvironment (TME), which becomes progressively immunosuppressive. The clinical success of immune checkpoint blockade therapies is limited to a small set of CRCs with high tumor mutational load and tumor-infiltrating T cells. Induction of immunogenic cell death (ICD), a type of cell death eliciting an immune response, can therefore help break the immunosuppressive TME, engage the innate components, and prime T cell-mediated adaptive immunity for long-term tumor control. In this review, we discuss the current understanding of ICD induced by antineoplastic agents, the influence of driver mutations, and recent developments to harness ICD in colon cancer. Mechanism-guided combinations of ICD-inducing agents with immunotherapy and actionable biomarkers will likely offer more tailored and durable benefits to patients with colon cancer.

摘要

结直肠癌(CRC)是全球癌症相关死亡的主要原因。结肠黏膜构成了一个关键的屏障和主要的免疫调节部位。免疫系统在癌症的发生和治疗中起着重要的作用,慢性感染或炎症引起的免疫激活众所周知会增加癌症的风险。在肿瘤发展过程中,肿瘤细胞不断与肿瘤微环境(TME)相互作用并塑造其形态,使 TME 逐渐失去免疫能力。免疫检查点阻断疗法的临床成功仅限于一小部分具有高肿瘤突变负荷和肿瘤浸润性 T 细胞的 CRC。因此,诱导免疫原性细胞死亡(ICD),即引发免疫反应的一种细胞死亡类型,可以帮助打破免疫抑制性 TME,激活先天成分,并为长期肿瘤控制引发 T 细胞介导的适应性免疫。在这篇综述中,我们讨论了抗肿瘤药物诱导 ICD 的最新理解、驱动突变的影响以及利用 ICD 治疗结肠癌的最新进展。基于机制的 ICD 诱导剂与免疫疗法和可操作生物标志物的联合应用,可能为结肠癌患者提供更具针对性和更持久的获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64f9/7593824/21ccf7c7f1c6/nihms-1577710-f0001.jpg

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