Prostaglandin E2 Signaling: Alternative Target for Glioblastoma?

Prostaglandin E2 Signaling: Alternative Target for Glioblastoma?
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DOI:
10.1016/j.trecan.2016.12.002
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发表时间:
2017-03
期刊:
影响因子:
18.4
通讯作者:
Shi Z
Shi Z
中科院分区:
医学1区
文献类型:
--
作者:
Jiang J;Qiu J;Li Q;Shi Z

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环氧合酶-2(COX-2)的升高和脑内相关的炎症有助于胶质母细胞瘤的发展。然而,COX抑制剂在胶质母细胞瘤治疗中的医学应用一直受到限制,因为它们的血管毒性已经得到很好的证明,而且最近的人类研究结果不一致。前列腺素E_2(PGE_2)已成为COX-2级联驱动的胶质瘤形成的主要介体。PGE2末端合成酶和受体是治疗胶质母细胞瘤的可行靶点吗?
Elevated cyclooxygenase-2 (COX-2) and the associated inflammation within the brain contribute to glioblastoma development. However, medical use of COX inhibitors in glioblastoma treatment has been limited due to their well-documented vascular toxicity and inconsistent outcomes from recent human studies. Prostaglandin E2 (PGE2) has emerged as a principal mediator for COX-2 cascade-driven gliomagenesis. Are PGE2 terminal synthases and receptors feasible therapeutic targets for glioblastoma?
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