Department of Hematology & Oncology, Pontificia Universidad Católica de Chile, Santiago 8330034, Chile.
Advanced Center for Chronic Diseases (ACCDiS), Pontificia Universidad Católica de Chile, Santiago 8330034, Chile.
Int J Mol Sci. 2020 Dec 12;21(24):9472. doi: 10.3390/ijms21249472.
Reprimo-like () is an uncharacterized member of the Reprimo gene family. Here, we evaluated the role of and whether its regulation by DNA methylation is a potential non-invasive biomarker of gastric cancer. RPRML expression was evaluated by immunohistochemistry in 90 patients with gastric cancer and associated with clinicopathologic characteristics and outcomes. The role of in cancer biology was investigated in vitro, through ectopic overexpression. Functional experiments included colony formation, soft agar, MTS, and Ki67 immunofluorescence assays. DNA methylation-mediated silencing was evaluated by the 5-azacytidine assay and direct bisulfite sequencing. Non-invasive detection of circulating methylated DNA was assessed in 25 gastric cancer cases and 25 age- and sex-balanced cancer-free controls by the MethyLight assay. Downregulation of RPRML protein expression was associated with poor overall survival in advanced gastric cancer. overexpression significantly inhibited clonogenic capacity, anchorage-independent growth, and proliferation in vitro. Circulating methylated DNA distinguished patients with gastric cancer from controls with an area under the curve of 0.726. The in vitro overexpression results and the poor patient survival associated with lower RPRML levels suggest that RPRML plays a tumor-suppressive role in the stomach. Circulating methylated DNA may serve as a biomarker for the non-invasive detection of gastric cancer.
Reprimo-like () 是 Reprimo 基因家族的一个未被描述的成员。在这里,我们评估了 的作用,以及其 DNA 甲基化调控是否是胃癌潜在的非侵入性生物标志物。通过免疫组织化学在 90 例胃癌患者中评估了 RPRML 的表达,并将其与临床病理特征和结果相关联。通过异位过表达,在体外研究了 在癌症生物学中的作用。功能实验包括集落形成、软琼脂、MTS 和 Ki67 免疫荧光检测。通过 5-氮杂胞苷测定和直接亚硫酸氢盐测序评估了 DNA 甲基化介导的沉默。通过 MethyLight 测定在 25 例胃癌病例和 25 例年龄和性别匹配的无癌对照中评估了循环甲基化 DNA 的非侵入性检测。RPRML 蛋白表达下调与晚期胃癌患者的总生存期不良相关。 过表达显著抑制了体外集落形成能力、锚定非依赖性生长和增殖。循环甲基化 DNA 可区分胃癌患者和对照组,曲线下面积为 0.726。体外过表达结果以及与较低 RPRML 水平相关的患者生存不良表明,RPRML 在胃中发挥肿瘤抑制作用。循环甲基化 DNA 可能作为胃癌非侵入性检测的生物标志物。