Koudonas Antonios, Dimitriadis Georgios, Anastasiadis Anastasios, Papaioannou Maria
First Department of Urology, School of Medicine, Faculty of Health Sciences, Aristotle University of Thessaloniki, 541 24 Thessaloniki, Greece.
Laboratory of Biological Chemistry, School of Medicine, Faculty of Health Sciences, Aristotle University of Thessaloniki, 541 24 Thessaloniki, Greece.
Epigenomes. 2024 Jul 15;8(3):28. doi: 10.3390/epigenomes8030028.
Patient response after treatment of renal cell cancer (RCC) with systemic agents, which include various drug categories, is generally poor and unpredictable. In this context, the ideal drug administration includes tools to predict the sensitivity of the disease to therapy. The aim of this study was to systematically summarize the reports on the predictive value of the methylation status in the systemic therapy of RCC. Only original articles reporting on the association of promoter methylation with the response of patients or cell lines to systemic agents were included in this review. We applied PRISMA recommendations to the structure and methodology of this systematic review. Our literature search concluded with 31 articles conducted on RCC cell lines and patient tissues. The majority of the studies demonstrated a methylation-dependent response to systemic agents. This correlation suggests that the methylation pattern can be used as a predictive tool in the management of RCC with various classes of systemic agents. However, although methylation biomarkers show promise for predicting response, the evidence of such correlation is still weak. More studies on the gene methylation pattern in patients under systemic therapy and its correlation with different degrees of response are needed.
肾细胞癌(RCC)经全身用药治疗后的患者反应通常较差且不可预测,全身用药包括多种药物类别。在此背景下,理想的药物治疗需要具备预测疾病对治疗敏感性的工具。本研究的目的是系统总结关于甲基化状态在RCC全身治疗中预测价值的报告。本综述仅纳入了报道启动子甲基化与患者或细胞系对全身用药反应之间关联的原创文章。我们将PRISMA建议应用于本系统综述的结构和方法。我们的文献检索最终得到了31篇关于RCC细胞系和患者组织的文章。大多数研究表明对全身用药存在甲基化依赖性反应。这种相关性表明甲基化模式可作为使用各类全身用药治疗RCC的预测工具。然而,尽管甲基化生物标志物在预测反应方面显示出前景,但这种相关性的证据仍然薄弱。需要对接受全身治疗的患者的基因甲基化模式及其与不同反应程度的相关性进行更多研究。