Pesce Silvia, Greppi Marco, Ferretti Elisa, Obino Valentina, Carlomagno Simona, Rutigliani Mariangela, Thoren Fredrik B, Sivori Simona, Castagnola Patrizio, Candiani Simona, Marcenaro Emanuela
Department of Experimental Medicine, University of Genoa, Genoa, Italy.
Center of Excellence for Biomedical Research, University of Genoa, Genoa, Italy.
Front Cell Dev Biol. 2020 Feb 25;8:119. doi: 10.3389/fcell.2020.00119. eCollection 2020.
The incidence of certain forms of tumors has increased progressively in recent years and is expected to continue growing as life expectancy continues to increase. Tumor-infiltrating NK cells may contribute to develop an anti-tumor response. Optimized combinations of different cancer therapies, including NK cell-based approaches for targeting tumor cells, have the potential to open new avenues in cancer immunotherapy. Functional inhibitory receptors on NK cells are needed to prevent their attack on healthy cells. Nevertheless, disruption of inhibitory receptors function on NK cells increases the cytotoxic capacity of NK cells against cancer cells. MicroRNAs (miRNAs) are small non-coding RNA molecules that target mRNA and thus regulate the expression of genes involved in the development, maturation, and effector functions of NK cells. Therapeutic strategies that target the regulatory effects of miRNAs have the potential to improve the efficiency of cancer immunotherapy. Interestingly, emerging evidence points out that some miRNAs can, directly and indirectly, control the surface expression of immune checkpoints on NK cells or that of their ligands on tumor cells. This suggests a possible use of miRNAs in the context of anti-tumor therapy. This review provides the current overview of the connections between miRNAs and regulation of NK cell functions and discusses the potential of these miRNAs as innovative biomarkers/targets for cancer immunotherapy.
近年来,某些类型肿瘤的发病率呈逐渐上升趋势,并且随着预期寿命的持续增加,预计还将继续增长。肿瘤浸润性自然杀伤(NK)细胞可能有助于产生抗肿瘤反应。包括基于NK细胞靶向肿瘤细胞的方法在内的不同癌症治疗方法的优化组合,有可能为癌症免疫治疗开辟新途径。NK细胞上的功能性抑制性受体可防止其攻击健康细胞。然而,NK细胞上抑制性受体功能的破坏会增加NK细胞对癌细胞的细胞毒性能力。微小RNA(miRNA)是靶向mRNA的小非编码RNA分子,从而调节参与NK细胞发育、成熟和效应功能的基因表达。针对miRNA调节作用的治疗策略有可能提高癌症免疫治疗的效率。有趣的是,新出现的证据指出,一些miRNA可以直接或间接控制NK细胞上免疫检查点的表面表达或肿瘤细胞上其配体的表面表达。这表明miRNA在抗肿瘤治疗中可能具有应用价值。本综述提供了miRNA与NK细胞功能调节之间联系的当前概述,并讨论了这些miRNA作为癌症免疫治疗创新生物标志物/靶点的潜力。