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解析癌症中CD8 + T细胞与微小RNA信号传导的相互作用:对免疫功能障碍和治疗方法的启示

Unraveling the interplay of CD8 + T cells and microRNA signaling in cancer: implications for immune dysfunction and therapeutic approaches.

作者信息

Zabeti Touchaei Arefeh, Vahidi Sogand

机构信息

Department of Chemistry, Lahijan Branch, Islamic Azad University, Lahijan, Iran.

Medical Biology Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.

出版信息

J Transl Med. 2024 Dec 20;22(1):1131. doi: 10.1186/s12967-024-05963-5.

Abstract

MicroRNAs (miRNAs) emerge as critical regulators of CD8 + T cell function within the complex tumor microenvironment (TME). This review explores the multifaceted interplay between miRNAs and CD8 + T cells across various cancers. We discuss how specific miRNAs influence CD8 + T cell activation, recruitment, infiltration, and effector function. Dysregulation of these miRNAs can contribute to CD8 + T cell exhaustion and immune evasion, hindering anti-tumor immunity. Conversely, manipulating miRNA expression holds promise for enhancing CD8 + T cell activity and improving cancer immunotherapy outcomes. We delve into the role of miRNAs in CD8 + T-cell function across different cancer types, including gliomas, gastric and colon cancer, oral squamous cell carcinoma, thyroid carcinoma, lymphomas, melanoma, breast cancer, renal cell carcinoma, ovarian cancer, uterine corpus endometrial cancer, bladder cancer, acute myeloid leukemia, chronic myelogenous leukemia, and osteosarcoma. Additionally, we explore how extracellular vesicles and cytokines modulate CD8 + T-cell function through complex interactions with miRNAs. Finally, we discuss the potential impact of radiotherapy and specific drugs on miRNA expression and CD8 + T-cell activity within the TME. This review highlights the immense potential of targeting miRNAs to manipulate CD8 + T-cell activity for the development of novel and improved cancer immunotherapies.

摘要

微小RNA(miRNA)在复杂的肿瘤微环境(TME)中成为CD8 + T细胞功能的关键调节因子。本综述探讨了miRNA与CD8 + T细胞在各种癌症中的多方面相互作用。我们讨论了特定的miRNA如何影响CD8 + T细胞的激活、募集、浸润和效应功能。这些miRNA的失调会导致CD8 + T细胞耗竭和免疫逃逸,从而阻碍抗肿瘤免疫。相反,操纵miRNA的表达有望增强CD8 + T细胞活性并改善癌症免疫治疗效果。我们深入探讨了miRNA在不同癌症类型(包括神经胶质瘤、胃癌和结肠癌、口腔鳞状细胞癌、甲状腺癌、淋巴瘤、黑色素瘤、乳腺癌、肾细胞癌、卵巢癌、子宫内膜癌、膀胱癌、急性髓细胞白血病、慢性粒细胞白血病和骨肉瘤)的CD8 + T细胞功能中的作用。此外,我们还探讨了细胞外囊泡和细胞因子如何通过与miRNA的复杂相互作用来调节CD8 + T细胞功能。最后,我们讨论了放疗和特定药物对TME内miRNA表达和CD8 + T细胞活性的潜在影响。本综述强调了靶向miRNA以操纵CD8 + T细胞活性以开发新型和改进的癌症免疫疗法的巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfe1/11662517/f7f7ef1a83dc/12967_2024_5963_Fig1_HTML.jpg

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