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Inhibition of GPR137 suppresses proliferation of medulloblastoma cells in vitro

机译:抑制GPR137在体外可抑制髓母细胞瘤细胞的增殖

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Medulloblastoma is the most common malignant pediatric brain tumor in children. GPR137 is a ubiquitously expressed gene in the central nervous system. It has been reported that GPR137 modulates malignant proliferation of glioma cells. However, the relationship between GPR137 and medulloblastoma is still unknown. In this study, we knocked down GPR137 in the medulloblastoma cell line Daoy via a lentivirus-based RNA interference system to explore its role in medulloblastoma. Functional analyses showed that cell proliferation and colony formation were obviously restrained in Daoy cells after GPR137 knockdown. Furthermore, knockdown of GPR137 in Daoy cells led to a significant increase in cell percentage in the G0/G1 phase but a decrease in the S phase. Additionally, the cell population in the sub-G1 phase, which represents apoptotic cells, was remarkably increased in GPR137 knockdown cells. GPR137 inhibition induced a strong proapoptotic effect in Daoy cells, as confirmed by annexin V-APC/7-AAD double staining. In conclusion, GPR137 knockdown inhibited growth of Daoy medulloblastoma cells via disturbing cell cycle progression and inducing apoptosis. Our investigation suggested that GPR137 could be a potential oncogene in medulloblastoma cells and might serve as a target for the treatment of medulloblastoma. (C) 2014 International Union of Biochemistry and Molecular Biology, Inc.
机译:髓母细胞瘤是儿童中最常见的恶性小儿脑肿瘤。 GPR137是中枢神经系统中普遍表达的基因。据报道,GPR137调节神经胶质瘤细胞的恶性增殖。但是,GPR137与髓母细胞瘤之间的关系仍然未知。在这项研究中,我们通过基于慢病毒的RNA干扰系统敲除了髓母细胞瘤细胞系Daoy中的GPR137,以探索其在髓母细胞瘤中的作用。功能分析表明,GPR137敲低后,Daoy细胞的细胞增殖和集落形成受到明显抑制。此外,在Daoy细胞中敲低GPR137导致G0 / G1期细胞百分比显着增加,但S期细胞减少。此外,在GPR137敲低细胞中,代表凋亡细胞的sub-G1期细胞数量显着增加。如膜联蛋白V-APC / 7-AAD双重染色所证实的,GPR137抑制在Daoy细胞中诱导了强的促凋亡作用。总之,GPR137敲低通过干扰细胞周期进程和诱导细胞凋亡来抑制Daoy髓母细胞瘤细胞的生长。我们的研究表明,GPR137可能是髓母细胞瘤细胞中潜在的癌基因,并可能成为治疗髓母细胞瘤的靶标。 (C)2014国际生物化学与分子生物学联合会

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