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首页> 外文期刊>Expert opinion on therapeutic targets >PKCeta as a therapeutic target in glioblastoma multiforme.
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PKCeta as a therapeutic target in glioblastoma multiforme.

机译:PKCeta作为胶质母细胞瘤的治疗靶标。

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摘要

Gliomas are the most common major subgroup of primary CNS tumours. Approximately 17,000 new cases are reported each year and, of these, 11,500 patients die. Glioblastoma multiforme (GBM) is highly proliferative and typically invades distal portions of the brain, thereby making complete surgical resection of these tumours nearly impossible. Moreover, GBMs are often resistant to current chemotherapy and radiation regimens. Therefore, there is a need for better therapeutic interventions. One class of proteins that is involved in the formation of malignant brain tumours is protein kinase C (PKC) and these kinases have not been thoroughly explored for their chemotherapeutic value in GBMs. The PKC isozyme, PKCeta (PKC-eta) increases cell proliferation and resistance to radiation of GBM cell lines. These properties make PKCeta an attractive target for chemotherapeutic intervention in the management of GBMs.
机译:神经胶质瘤是原发性中枢神经系统肿瘤最常见的主要亚组。每年报告约17,000例新病例,其中11,500例患者死亡。多形胶质母细胞瘤(GBM)高度增殖,通常会侵袭大脑的远端,因此几乎不可能完全切除这些肿瘤。而且,GBM经常对当前的化学疗法和放射疗法有抵抗力。因此,需要更好的治疗干预。参与恶性脑肿瘤形成的一类蛋白质是蛋白激酶C(PKC),尚未就这些激酶在GBM中的化学治疗价值进行深入研究。 PKC同工酶PKCeta(PKC-eta)可以增加细胞增殖以及对GBM细胞系辐射的抵抗力。这些特性使PKCeta成为GBM管理中化学疗法干预的诱人靶标。

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