Cancer Biology and Epigenetics Group, IPO Porto Research Center (CI-IPOP), Portuguese Oncology Institute of Porto (IPO Porto), Porto 4200-072, Portugal; Institute of Biomedical Sciences Abel Salazar, University of Porto (ICBAS-UP), Rua Jorge Viterbo Ferreira 228, 4050-513 Porto, Portugal.
Cancer Biology and Epigenetics Group, IPO Porto Research Center (CI-IPOP), Portuguese Oncology Institute of Porto (IPO Porto), Porto 4200-072, Portugal.
Biomed Pharmacother. 2021 Sep;141:111681. doi: 10.1016/j.biopha.2021.111681. Epub 2021 Jun 15.
Renal Cell Carcinoma (RCC) is on the top 10 of the most incident cancers worldwide, being a third of patients diagnosed with advanced disease, for which no curative therapies are currently available. Thus, new effective therapeutic strategies are urgently needed. Herein, we tested the antineoplastic effect of newly synthesized 3-nitroflavanones (MLo1302) on RCC cell lines. 786-O, Caki2, and ACHN cell lines were cultured and treated with newly synthesized 3-nitroflavanones. IC50 values were calculated based on the effect on cell viability assessed by MTT assay, after 72 h of exposure. MLo1302 displayed antineoplastic properties in RCC cell lines through marked reduction of cell viability, increased apoptosis and DNA damage, and morphometric alterations indicating a less aggressive phenotype. MLo1302 induced a significant reduction of global DNA methylation and DNMT mRNA levels, increasing global DNA hydroxymethylation and TET expression. Moreover, MLo1302 decreased DNMT3A activity in RCC cell lines, demethylated and re-expressed hypermethylated genes in CAM-generated tumors. A marked in vivo decrease in tumor growth and angiogenesis was also disclosed. MLo1302 disclosed antineoplastic and demethylating activity in RCC cell lines, constituting a potential therapeutic agent for RCC patients.
肾细胞癌 (RCC) 是全球发病率最高的癌症前 10 位之一,约有三分之一的患者被诊断为晚期疾病,目前尚无有效的治疗方法。因此,迫切需要新的有效的治疗策略。在此,我们测试了新合成的 3-硝基黄酮(MLo1302)对 RCC 细胞系的抗肿瘤作用。培养 786-O、Caki2 和 ACHN 细胞系,并使用新合成的 3-硝基黄酮进行处理。根据 MTT 测定评估的细胞活力效应,计算出 IC50 值,暴露 72 小时后。MLo1302 通过显著降低细胞活力、增加细胞凋亡和 DNA 损伤以及形态学改变,表现出对 RCC 细胞系的抗肿瘤特性,表明其具有侵袭性较小的表型。MLo1302 诱导了全球 DNA 甲基化和 DNMT mRNA 水平的显著降低,增加了全球 DNA 羟甲基化和 TET 表达。此外,MLo1302 降低了 RCC 细胞系中的 DNMT3A 活性,使 CAM 生成的肿瘤中甲基化的基因去甲基化并重新表达。体内肿瘤生长和血管生成也明显减少。MLo1302 在 RCC 细胞系中表现出抗肿瘤和去甲基化活性,是 RCC 患者的潜在治疗剂。