RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Mechanism and strategies of immunotherapy resistance in colorectal cancer.
Mechanism and strategies of immunotherapy resistance in colorectal cancer.
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结直肠癌(CRC)是全球第三大常见癌症。尽管CRC有标准治疗方案,但大多数患者对这些治疗反应不佳。随着对肿瘤免疫认识的不断深入,免疫治疗逐渐兴起,并在多种癌症中展现出良好的治疗效果。免疫治疗包括细胞因子、免疫检查点抑制剂(ICIs)和过继性细胞疗法。特别是针对细胞毒性T淋巴细胞相关蛋白4(CTLA-4)、程序性细胞死亡1(PD-1)或其配体PD-L1的抗体类ICIs,已成功应用于实体瘤的临床治疗,缓解了肿瘤微环境对T细胞的抑制作用。然而,只有少数癌症患者在免疫治疗期间获得持久的临床缓解。多种因素限制了免疫治疗的疗效,导致耐药性的产生。在本综述中,我们旨在讨论CRC免疫治疗的现状,并阐述介导免疫治疗耐药的机制及其他潜在的治疗策略。
Colorectal cancer (CRC) is the third most common cancer in the world. Although there are standard treatment options for CRC, most patients respond poorly to these treatments. Immunotherapies have gradually emerged due to the increasing awareness and understanding of tumor immunity, exhibiting good therapeutic efficacy in various cancers.
Immunotherapies include cytokines, immune checkpoint inhibitors (ICIs), and adoptive cell therapies. In particular, ICIs, which are antibodies against cytotoxic T lymphocyte-associated protein 4 (CTLA-4), programmed cell death 1 (PD-1), or its ligand PD-L1, have been successfully applied clinically for solid tumors, relieving the inhibitory effect of the tumor microenvironment on T cells.
However, only a minority of patients with cancer achieve a durable clinical response during immunotherapy. Several factors restrict the efficacy of immunotherapy, leading to the development of drug resistance. In this review, we aimed to discuss the current status of immunotherapy for CRC and elaborate on the mechanisms that mediate resistance to immunotherapy and other potential therapeutic strategies.
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