Department of Molecular Biology, Institute of Biotechnology, The John Paul II Catholic University of Lublin, ul. Konstantynów 1i, 20-708, Lublin, Poland.
Mol Cell Biochem. 2017 Nov;435(1-2):193-196. doi: 10.1007/s11010-017-3068-z. Epub 2017 May 13.
CX-4945 is a selective inhibitor of protein kinase CK2 exhibiting clinical significance. Its antitumor properties arise from the abrogation of CK2-mediated pro-survival cellular pathways. The presented data reveal the influence of CX-4945 on the growth of yeast cells showing variable potency against Saccharomyces cerevisiae deletion strains with different contents of CK2 subunits. The catalytic subunit CK2α appears to sensitize yeast to the CX-4945 action. Moreover, the compound suppresses hyphal growth and cell adhesion of Candida albicans, thereby abolishing some hallmarks of invasiveness of the pathogen. It is known that cancer patients are more prone to fungal infections. Our data unveil the dual-activity of CX-4945; when used in anti-cancer therapy, it may simultaneously prevent cancer-associated candidiasis.
CX-4945 是一种有临床意义的蛋白激酶 CK2 的选择性抑制剂。其抗肿瘤特性源于 CK2 介导的抗生存细胞通路的中断。所呈现的数据揭示了 CX-4945 对酵母细胞生长的影响,该化合物对不同 CK2 亚基含量的酿酒酵母缺失菌株表现出不同的效力。催化亚基 CK2α 似乎使酵母对 CX-4945 的作用敏感。此外,该化合物抑制白色念珠菌的菌丝生长和细胞黏附,从而消除病原体侵袭性的一些特征。众所周知,癌症患者更容易发生真菌感染。我们的数据揭示了 CX-4945 的双重活性;在癌症治疗中使用时,它可能同时预防与癌症相关的念珠菌病。