Laboratório de Hormônios e Genética Molecular LIM/42, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Unidade de Endocrinologia do Desenvolvimento & Unidade de Suprarrenal, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.
Horm Metab Res. 2021 Feb;53(2):124-131. doi: 10.1055/a-1322-2943. Epub 2020 Dec 11.
3-Hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR) is the rate-limiting enzyme of the mevalonate pathway, which generates cholesterol and non-sterol compounds such as isoprenoid, which are involved in key steps of tumorigenesis such as cell growth and proliferation. Our aim was to evaluate the role of the mevalonate pathway in adrenocortical tumors (ACTs). Expression pattern of , , , , , , , , , , and genes involved in the mevalonate pathway and steroidogenesis, was quantified by real-time RT-PCR in 46 ACT [14 adenomas (ACA) and 11 carcinomas (ACC) from adults and 13 ACA and 8 ACC from pediatric patients]. Effects of the mevalonate pathway inhibition on NCI-H295A cell viability was assessed by colorimetric assay. was overexpressed in most adult ACT. The expression of , , , , and in adult ACC was significantly lower than in ACA (p<0.05). Regarding pediatric ACT, the expression of genes involved in steroidogenesis was not different between ACA and ACC. Inhibition of isoprenoid production significantly decreased the viability of NCI-H295A cells (p<0.05). However, cholesterol synthesis blockage did not show the same effect on cell viability. Low expression of ,: , , , and characterized a signature of adult ACCs. Our data suggest that overexpression in adult ACC might lead to intracellular isoprenoid accumulation and cell proliferation. Therefore, the mevalonate pathway is a potential target for ACC treatment.
3-羟-3-甲基戊二酰基辅酶 A 还原酶(HMGCR)是甲羟戊酸途径的限速酶,该途径生成胆固醇和非甾体化合物,如异戊烯,参与肿瘤发生的关键步骤,如细胞生长和增殖。我们的目的是评估甲羟戊酸途径在肾上腺皮质肿瘤(ACTs)中的作用。通过实时 RT-PCR 定量分析了甲羟戊酸途径和类固醇生成中涉及的 、 、 、 、 、 、 、 、 基因在 46 例 ACT [14 例成人腺瘤(ACA)和 11 例癌(ACC)和 13 例儿童 ACA 和 8 例儿童 ACC]中的表达模式。通过比色法评估甲羟戊酸途径抑制对 NCI-H295A 细胞活力的影响。 在大多数成人 ACT 中过表达。成人 ACC 中 、 、 、 和 的表达明显低于 ACA(p<0.05)。关于儿科 ACT,ACA 和 ACC 之间类固醇生成相关基因的表达没有差异。异戊烯产生的抑制显著降低了 NCI-H295A 细胞的活力(p<0.05)。然而,胆固醇合成阻断对细胞活力没有相同的影响。 、 、 、 和 的低表达特征是成人 ACC 的特征。我们的数据表明,成人 ACC 中的 过表达可能导致细胞内异戊烯积累和细胞增殖。因此,甲羟戊酸途径是 ACC 治疗的潜在靶点。