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晚期肾细胞癌中的表观遗传学:潜在的新靶点。

Epigenetics in advanced renal cell carcinoma: Potential new targets.

机构信息

Medical Oncology Department, Hospital Universitario Ramón y Cajal, Medicine School, Alcalá University, Madrid, Spain.

Oncology Unit, Macerata Hospital, Macerata, Italy.

出版信息

Crit Rev Oncol Hematol. 2022 Dec;180:103857. doi: 10.1016/j.critrevonc.2022.103857. Epub 2022 Oct 17.

Abstract

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.

摘要

肾细胞癌(RCC)是欧洲成年人第七大常见肿瘤,约占癌症死亡人数的 2.5%。在转移性疾病中,包括酪氨酸激酶抑制剂抑制血管生成以及针对免疫检查点蛋白(如 PD-1/PDL-1 和 CTLA-4)的免疫治疗在内的临床策略已经彻底改变了治疗格局。不幸的是,大多数患者对抗血管生成和免疫治疗进展。RCC 中经常发现表观遗传异常,表明表观遗传修饰的改变,如启动子甲基化或异常 microRNA 表达,是由于基因表达改变而基因组序列不变导致 RCC 发生的关键。如今,表观遗传学领域的新药能够修饰基因表达,从而在肿瘤细胞中诱导抗肿瘤作用。在肾癌中,针对表观遗传学的药物处于早期开发阶段,但在不久的将来可能会有希望。在这篇综述中,我们总结了在 RCC 中发现的主要表观遗传改变及其在病理信号通路中的参与,这是一个新的潜在靶点,可能会被添加到晚期 RCC 患者的治疗流程中。

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