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脑脂质结合蛋白在体外通过调节ERK1/2信号通路介导人胶质母细胞瘤细胞的增殖。

Brain lipid binding protein mediates the proliferation of human glioblastoma cells by regulating ERK1/2 signaling pathway in vitro.

作者信息

Tian Wei, Shi Jinhong, Qin Jianbing, Jin Guohua, Han Xiao, Li Haoming

机构信息

Department of Pathology, Affiliated Hospital of Nantong University, Nantong, 226001, China.

Department of Human Anatomy, Medical School, Nantong University, Nantong, 226001, China.

出版信息

In Vitro Cell Dev Biol Anim. 2018 Feb;54(2):156-162. doi: 10.1007/s11626-017-0220-8. Epub 2017 Dec 29.

Abstract

Brain lipid binding protein (BLBP) is highly expressed in the radial glial cells (RGCs) of the central nervous system (CNS), in glioblastomas, and, in vitro, in U251 cells. In this report, we have demonstrated that increased BLBP expression in glioblastoma is associated with poor survival and used a double-vector CRISPR/Cas9 lentiviral system to deplete endogenous BLBP from U251 cells, we found that loss of BLBP induced cell growth inhibition and S-phase arrest. Moreover, an increase in P53 and a decrease in p-ERK1/2 were observed after BLBP depletion, suggesting a potential mechanism by which loss of BLBP results in growth inhibition.

摘要

脑脂质结合蛋白(BLBP)在中枢神经系统(CNS)的放射状胶质细胞(RGCs)、胶质母细胞瘤中以及体外培养的U251细胞中高表达。在本报告中,我们证明胶质母细胞瘤中BLBP表达增加与生存率低相关,并使用双载体CRISPR/Cas9慢病毒系统从U251细胞中去除内源性BLBP,我们发现BLBP缺失诱导细胞生长抑制和S期阻滞。此外,BLBP缺失后观察到P53增加和p-ERK1/2减少,提示BLBP缺失导致生长抑制的潜在机制。

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