MicroRNAs as regulators of immune checkpoints in cancer immunotherapy: targeting PD-1/PD-L1 and CTLA-4 pathways

被引:38
作者
Touchaei, Arefeh Zabeti [1 ]
Vahidi, Sogand [2 ]
机构
[1] Islamic Azad Univ, Dept Chem, Lahijan Branch, Lahijan, Iran
[2] Kermanshah Univ Med Sci, Med Biol Res Ctr, Kermanshah, Iran
关键词
Immune checkpoint inhibitors; Immunotherapy; PD-1; PD-L1; CTLA-4; microRNA; CELL LUNG-CANCER; NEGATIVE BREAST-CANCER; PD-L1; EXPRESSION; COLORECTAL-CANCER; TUMOR PROGRESSION; UP-REGULATION; T-CELLS; BLOCKADE; ESCAPE; PROLIFERATION;
D O I
10.1186/s12935-024-03293-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunotherapy has revolutionized cancer treatment by harnessing the power of the immune system to eliminate tumors. Immune checkpoint inhibitors (ICIs) block negative regulatory signals that prevent T cells from attacking cancer cells. Two key ICIs target the PD-1/PD-L1 pathway, which includes programmed death-ligand 1 (PD-L1) and its receptor programmed death 1 (PD-1). Another ICI targets cytotoxic T-lymphocyte-associated protein 4 (CTLA-4). While ICIs have demonstrated remarkable efficacy in various malignancies, only a subset of patients respond favorably. MicroRNAs (miRNAs), small non-coding RNAs that regulate gene expression, play a crucial role in modulating immune checkpoints, including PD-1/PD-L1 and CTLA-4. This review summarizes the latest advancements in immunotherapy, highlighting the therapeutic potential of targeting PD-1/PD-L1 and CTLA-4 immune checkpoints and the regulatory role of miRNAs in modulating these pathways. Consequently, understanding the complex interplay between miRNAs and immune checkpoints is essential for developing more effective and personalized immunotherapy strategies for cancer treatment.
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页数:32
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