Montenarh Mathias
Medical Biochemistry and Molecular Biology, Saarland University, Homburg.
Adv Clin Exp Med. 2014 Mar-Apr;23(2):153-8. doi: 10.17219/acem/37040.
CK2 is an ubiquitously expressed protein kinase, which is composed of two catalytic a- and a'- and two noncatalytic b-subunits. CK2 protein levels and kinase activity is elevated in rapidly proliferating cells including cancer cells. There is increasing evidence that CK2 also plays an essential role in angiogenesis, either by interaction or phosphorylation of growth factors or by phosphorylation or binding to proteins in signalling cascades, which are implicated in angiogenesis. Over the last ten years a great number of inhibitors for CK2 were detected, two of them are now in clinical phase II trials for the treatment of cancer patients. Some of these inhibitors were also found to be active in the inhibition of angiogenesis. Thus, CK2 inhibitors probably together with inhibitors of other signalling molecules involved in angiogenesis might be powerful tools for the treatment of cancer and cancer connected angiogenesis.
CK2是一种广泛表达的蛋白激酶,由两个催化性的α和α'亚基以及两个非催化性的β亚基组成。在包括癌细胞在内的快速增殖细胞中,CK2蛋白水平和激酶活性会升高。越来越多的证据表明,CK2在血管生成中也起着至关重要的作用,它可以通过与生长因子相互作用或使其磷酸化,或者通过磷酸化或结合信号级联反应中的蛋白质来实现,而这些都与血管生成有关。在过去十年中,人们发现了大量CK2抑制剂,其中两种目前正处于治疗癌症患者的II期临床试验阶段。还发现其中一些抑制剂在抑制血管生成方面具有活性。因此,CK2抑制剂可能与其他参与血管生成的信号分子抑制剂一起,成为治疗癌症和与癌症相关的血管生成的有力工具。