Inhibitors of CK2 Kinase for the Treatment of Gliomas and Other Brain Tumors

E. Pucko, Robert P. Ostrowski
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Abstract

Protein kinase CK2 has become a target of experimental antiglioma therapies as laboratory data are almost uniformly favorable and the number of synthetized CK2 inhibitors is rapidly growing. The evidence of their use for other brain tumors is on the increase as well. Great expectations are entrusted in naturally occurring compounds capable of inhibiting CK2 kinase. These compounds are extracted and purified by means of biochemistry methods and are amenable for innovative drug delivery systems as well. CK2 kinase inhibitors have been proven suitable for combined therapies with other investigational antiglioma agents and treatment modalities. However a greater share of efforts should be undertaken towards inhibiting functions relatively specific for glial tumors including infiltrative growth and invasiveness or maintenance of glioma initiating cells. Many of these function appear to converge on mTOR and JAK/STAT pathways which are being meticulously studied in this respect. Protein kinase CK2 holds therapeutic promise especially when combined with other agents aimed at molecular signatures of gliomas.
用于治疗胶质瘤和其他脑肿瘤的 CK2 激酶抑制剂
蛋白激酶 CK2 已成为实验性抗胶质瘤疗法的一个靶点,因为实验室数据几乎都是正面的,而且合成的 CK2 抑制剂的数量也在迅速增加。将它们用于其他脑肿瘤的证据也在增加。人们对能够抑制 CK2 激酶的天然化合物寄予厚望。这些化合物是通过生物化学方法提取和纯化的,也可用于创新的给药系统。事实证明,CK2 激酶抑制剂适合与其他研究中的抗胶质瘤药物和治疗方法联合使用。然而,更多的工作应致力于抑制胶质瘤相对特有的功能,包括胶质瘤始发细胞的浸润性生长和侵袭性或维持性。其中许多功能似乎都与 mTOR 和 JAK/STAT 通路有关,目前正在这方面进行细致的研究。蛋白激酶 CK2 具有治疗前景,尤其是与其他针对胶质瘤分子特征的药物联合使用时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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