MicroRNAs and dendritic cell-based vaccination in melanoma patients

被引:11
作者
De Rosa, Francesco [1 ]
Fanini, Francesca [2 ]
Guidoboni, Massimo [1 ]
Vannini, Ivan [2 ]
Amadori, Dino [3 ]
Ridolfi, Ruggero [1 ]
Ridolfi, Laura [1 ]
Fabbri, Muller [2 ,4 ,5 ]
机构
[1] Ist Sci Romagnolo Studio & Cura Tumori IRST IRCCS, Immunotherapy Unit, I-47014 Meldola, FC, Italy
[2] Ist Sci Romagnolo Studio & Cura Tumori IRST IRCCS, Gene Therapy Unit, I-47014 Meldola, FC, Italy
[3] Ist Sci Romagnolo Studio & Cura Tumori IRST IRCCS, Dept Med Oncol, I-47014 Meldola, FC, Italy
[4] Univ So Calif, Kenneth Norris Jr Comprehens Canc Ctr, Saban Res Inst, Dept Pediat & Mol Microbiol & Immunol, Los Angeles, CA 90033 USA
[5] Univ So Calif, Keck Sch Med, Childrens Hosp Los Angeles, Childrens Ctr Canc & Blood Dis, Los Angeles, CA 90033 USA
关键词
immunotherapy; microRNAs; melanoma; dendritic cell; anticancer vaccination; TRANSCRIPTION FACTOR; IMMUNE-RESPONSES; TARGET GENES; T-CELLS; EXPRESSION; MIR-155; CONTRIBUTES; INDUCTION; DIFFERENTIATION; PROGRESSION;
D O I
10.1097/CMR.0000000000000058
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs are increasingly being recognized to play an important role in finely tuning gene expression; therefore, their dysregulation in cancer has been investigated extensively. In terms of melanoma, they are involved in the regulation of many genes and pathways impacting invasiveness, dissemination, and disease progression. Many microRNAs also target genes regulating ontogenesis and functions of the immune system. Indeed, fine-tuning of gene expression by microRNAs is necessary for normal differentiation of the various components of the immune system and for mounting an effective innate and cell-mediated response, which has been shown to be able to control tumor growth. Dendritic cells, by presenting antigens to and activating naive T cells, constitute a critical aspect and have been therefore been used in many studies of cancer vaccination with promising results. Many genes regulating functions and plasticity of dendritic cells are indeed targeted by microRNAs, whose expression is also dependent on maturation status. Therefore, microRNAs could provide new potential therapeutic targets both on the tumor and on the immune system, and could also be used to characterize dendritic cells utilized in immunotherapy trials.
引用
收藏
页码:181 / 189
页数:9
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