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氨基酸剥夺诱导人胶质瘤细胞中环氧合酶-2表达需要p38丝裂原活化蛋白激酶

Cyclooxygenase-2 Induction by Amino Acid Deprivation Requires p38 Mitogen-Activated Protein Kinase in Human Glioma Cells.

作者信息

Li Zhiwen, Chang Chi-Ming, Wang Lanfang, Zhang Ping, Shu Hui-Kuo G

机构信息

a Department of Radiation Oncology and the Winship Cancer Institute , Emory University , Atlanta , Georgia , USA.

b Department of Anesthesiology , First Hospital of Jilin University , Changchun , China.

出版信息

Cancer Invest. 2017 Apr 21;35(4):237-247. doi: 10.1080/07357907.2017.1292517. Epub 2017 Mar 23.

Abstract

Glioblastomas (GBMs) are malignant brain tumors that can outstrip nutrient supplies due to rapid growth. Cyclooxygenase-2 (COX-2) has been linked to GBMs and may contribute to their aggressive phenotypes. Amino acid starvation results in COX-2 mRNA and protein induction in multiple human glioma cell lines in a process requiring p38 mitogen-activated protein kinase (p38-MAPK) and the Sp1 transcription factor. Increased vascular endothelial growth factor expression results from starvation-dependent COX-2 induction. These data suggest that COX-2 induction with amino acid deprivation may be a part of the adaptation of glioma cells to these conditions, and potentially alter cellular response to anti-neoplastic therapy.

摘要

胶质母细胞瘤(GBM)是恶性脑肿瘤,由于生长迅速,可能会耗尽营养供应。环氧合酶-2(COX-2)与GBM有关,可能促成其侵袭性表型。氨基酸饥饿会导致多种人类胶质瘤细胞系中COX-2 mRNA和蛋白质的诱导,这一过程需要p38丝裂原活化蛋白激酶(p38-MAPK)和Sp1转录因子。饥饿依赖性COX-2诱导导致血管内皮生长因子表达增加。这些数据表明,氨基酸剥夺诱导COX-2可能是胶质瘤细胞适应这些条件的一部分,并可能改变细胞对抗肿瘤治疗的反应。

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