表观遗传学
医学
癌症研究
肾细胞癌
小RNA
癌症
DNA甲基化
肾癌
肾透明细胞癌
血管生成
表观遗传疗法
免疫疗法
生物信息学
生物
肿瘤科
基因表达
基因
遗传学
作者
Javier Molina‐Cerrillo,Matteo Santoni,Álvaro J. Ruiz,Francesco Massari,Javier Pozas,Ignacio Ortego,Victoria Gómez,Enrique Grande,Teresa Alonso‐Gordoa
标识
DOI:10.1016/j.critrevonc.2022.103857
摘要
Renal cell carcinoma (RCC) is the seventh most frequently diagnosed tumor in adults in Europe and represents approximately 2.5 % of cancer deaths. In metastatic setting, clinical strategies including angiogenesis inhibition with tyrosine kinase inhibitors, as well as immunotherapy against immune checkpoint proteins, such as PD-1/PDL-1 and CTLA-4, have revolutionized the treatment landscape. Unfortunately, most patients progress to anti angiogenic and immunotherapy treatment. Epigenetic aberrations are commonly found in RCC, showing that changes in epigenetic modifications, like promoter methylation or abnormal microRNA expression, are key in the development of RCC due to gene expression alterations without changes in the genome sequence. Nowadays, new drugs in the field of epigenetics are able to modify gene expression to induce antitumoral effect in the tumor cell. In kidney cancer, drugs targeting epigenetics are in early development, but could be promising in the near future. In this review, we summarize the main epigenetic alterations found in RCC and their involvement in pathological signaling pathways, being a new potential target that could potentially be added to the treatment flow of patients with advanced RCC.
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