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锌指蛋白36通过下调恶性胶质瘤细胞中的白细胞介素-8和血管内皮生长因子发挥作用。

Tristetraprolin down-regulates interleukin-8 and vascular endothelial growth factor in malignant glioma cells.

作者信息

Suswam Esther, Li Yanyan, Zhang Xiaowen, Gillespie G Yancey, Li Xuelin, Shacka John J, Lu Liang, Zheng Lei, King Peter H

机构信息

Department of Neurology, University of Alabama, Birmingham, Alabama 35294-0017, USA.

出版信息

Cancer Res. 2008 Feb 1;68(3):674-82. doi: 10.1158/0008-5472.CAN-07-2751.

Abstract

Malignant gliomas are highly aggressive tumors of the central nervous system that rely on production of growth factors for tumor progression. Vascular endothelial growth factor (VEGF), interleukin-8 (IL-8), and tumor necrosis factor-alpha, for example, are up-regulated in these tumors to promote angiogenesis and proliferation. RNA stability, mediated through adenine and uridine-rich elements (ARE) in the 3' untranslated region, is a critical control point for regulating these growth factors. RNA half-life is predominantly governed by a balance between stabilizing and destabilizing factors that bind to ARE. We have previously shown that the stabilizing factor HuR is overexpressed in malignant gliomas and linked to RNA stabilization of angiogenic growth factors. Here, we report that the destabilizing factor tristetraprolin (TTP) is also ubiquitously expressed in primary malignant glioma tissues and cell lines. In contrast to benign astrogliotic tissues, however, the protein was hyperphosphorylated, with evidence implicating the p38/mitogen-activated protein kinase (MAPK) pathway. Conditional overexpression of TTP as a transgene in malignant glioma cells led to RNA destabilization of IL-8 and VEGF and down-regulation of protein production. Analysis of in vivo RNA binding indicated a shift of mRNA toward ectopic TTP and away from endogenous HuR. This biochemical phenotype was associated with a decrease in cell proliferation, loss of cell viability, and apoptosis. We postulate that hyperphosphorylation of TTP via p38/MAPK promotes progression of malignant gliomas by negatively regulating its RNA destabilizing function.

摘要

恶性胶质瘤是中枢神经系统中极具侵袭性的肿瘤,其肿瘤进展依赖于生长因子的产生。例如,血管内皮生长因子(VEGF)、白细胞介素-8(IL-8)和肿瘤坏死因子-α在这些肿瘤中上调,以促进血管生成和增殖。通过3'非翻译区富含腺嘌呤和尿嘧啶的元件(ARE)介导的RNA稳定性是调节这些生长因子的关键控制点。RNA半衰期主要由与ARE结合的稳定和不稳定因子之间的平衡决定。我们之前已经表明,稳定因子HuR在恶性胶质瘤中过表达,并与血管生成生长因子的RNA稳定有关。在此,我们报告不稳定因子锌指蛋白36(TTP)在原发性恶性胶质瘤组织和细胞系中也普遍表达。然而,与良性星形胶质细胞组织相比,该蛋白发生了过度磷酸化,有证据表明与p38/丝裂原活化蛋白激酶(MAPK)途径有关。在恶性胶质瘤细胞中作为转基因条件性过表达TTP导致IL-8和VEGF的RNA不稳定以及蛋白质产生的下调。体内RNA结合分析表明mRNA向异位TTP转移,远离内源性HuR。这种生化表型与细胞增殖减少、细胞活力丧失和细胞凋亡有关。我们推测,通过p38/MAPK对TTP的过度磷酸化通过负调节其RNA不稳定功能促进恶性胶质瘤的进展。

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