Cancer Genetics and Epigenetics Research Group, Department of Biosciences, COMSATS University Islamabad, Islamabad, Pakistan.
Department of Rheumatology, Military hospital, Rawalpindi, Pakistan.
PLoS One. 2023 Feb 21;18(2):e0281840. doi: 10.1371/journal.pone.0281840. eCollection 2023.
Mitochondrial sirtuins have diverse role specifically in aging, metabolism and cancer. In cancer, these sirtuins play dichotomous role as tumor suppressor and promoter. Previous studies have reported the involvement of sirtuins in different cancers. However, till now no study has been published with respect to mitochondrial sirtuins and glioma risks. Present study was purposed to figure out the expression level of mitochondrial sirtuins (SIRT3, SIRT4, SIRT5) and related genes (GDH, OGG1-2α, SOD1, SOD2, HIF1α and PARP1) in 153 glioma tissue samples and 200 brain tissue samples from epilepsy patients (taken as controls). To understand the role of selected situins in gliomagenesis, DNA damage was measured using the comet assay and oncometabolic role (oxidative stress level, ATP level and NAD level) was measured using the ELISA and quantitative PCR. Results analysis showed significant down-regulation of SIRT4 (p = 0.0337), SIRT5 (p<0.0001), GDH (p = 0.0305), OGG1-2α (p = 0.0001), SOD1 (p<0.0001) and SOD2 (p<0.0001) in glioma patients compared to controls. In case of SIRT3 (p = 0.0322), HIF1α (p = 0.0385) and PARP1 (p = 0.0203), significant up-regulation was observed. ROC curve analysis and cox regression analysis showed the good diagnostic and prognostic value of mitochondrial sirtuins in glioma patients. Oncometabolic rate assessment analysis showed significant increased ATP level (p<0.0001), NAD+ level [(NMNAT1 (p<0.0001), NMNAT3 (p<0.0001) and NAMPT (p<0.04)] and glutathione level (p<0.0001) in glioma patients compared to controls. Significant increased level of damage ((p<0.04) and decrease level of antioxidant enzymes include superoxide dismutase (SOD, p<0.0001), catalase (CAT, p<0.0001) and glutathione peroxidase (GPx, p<0.0001) was observed in patients compared to controls. Present study data suggest that variation in expression pattern of mitochondrial sirtuins and increased metabolic rate may have diagnostic and prognostic significance in glioma patients.
线粒体中的沉默调节蛋白在衰老、代谢和癌症中具有多种作用。在癌症中,这些沉默调节蛋白具有抑癌和促癌的双重作用。之前的研究已经报道了沉默调节蛋白在不同癌症中的作用。然而,到目前为止,还没有关于线粒体沉默调节蛋白与神经胶质瘤风险的研究发表。本研究旨在探讨 153 例神经胶质瘤组织样本和 200 例癫痫患者(作为对照)脑组织样本中线粒体沉默调节蛋白(SIRT3、SIRT4、SIRT5)和相关基因(GDH、OGG1-2α、SOD1、SOD2、HIF1α 和 PARP1)的表达水平。为了了解所选沉默调节蛋白在神经胶质瘤发生中的作用,使用彗星试验测量 DNA 损伤,使用 ELISA 和定量 PCR 测量致癌代谢作用(氧化应激水平、ATP 水平和 NAD 水平)。结果分析表明,与对照组相比,神经胶质瘤患者中 SIRT4(p = 0.0337)、SIRT5(p<0.0001)、GDH(p = 0.0305)、OGG1-2α(p = 0.0001)、SOD1(p<0.0001)和 SOD2(p<0.0001)表达显著下调。在 SIRT3(p = 0.0322)、HIF1α(p = 0.0385)和 PARP1(p = 0.0203)方面,观察到显著上调。ROC 曲线分析和 Cox 回归分析表明,线粒体沉默调节蛋白在神经胶质瘤患者中具有良好的诊断和预后价值。致癌代谢率评估分析表明,与对照组相比,神经胶质瘤患者的 ATP 水平(p<0.0001)、NAD+水平[(NMNAT1(p<0.0001)、NMNAT3(p<0.0001)和 NAMPT(p<0.04)]和谷胱甘肽水平(p<0.0001)显著升高。与对照组相比,患者的损伤水平(p<0.04)和抗氧化酶水平(超氧化物歧化酶[SOD],p<0.0001、过氧化氢酶[CAT],p<0.0001 和谷胱甘肽过氧化物酶[GPx],p<0.0001)显著降低。本研究数据表明,线粒体沉默调节蛋白表达模式的变化和代谢率的增加可能对神经胶质瘤患者具有诊断和预后意义。