Targeting protein kinases for anti-glioma treatment

被引:4
作者
Pucko, Emanuela B. [1 ]
Ostrowski, Robert P. [1 ]
机构
[1] Polish Acad Sci, Dept Expt & Clin Neuropathol, Mossakowski Med Res Ctr, 5 Pawinskiego St, PL-02106 Warsaw, Poland
关键词
glioblastoma; SEGA; protein kinase inhibitors; CK2; isothioureas; U87MG GLIOBLASTOMA CELLS; CK2; INHIBITORS; MALIGNANT-TRANSFORMATION; TUBEROUS SCLEROSIS; MOLECULAR PATHWAYS; SIGNALING PATHWAY; STEM-CELLS; RECEPTOR; CANCER; GROWTH;
D O I
10.5114/fn.2020.102430
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The genetic alterations related to many kinases are responsible for the formation of glial tumours. In addition it is the cell kinases that keep the cancerous signalling machinery in motion, thus enabling tumour cell growth, motility and invasion. Kinase inhibitors may have a potential to surpass the classical oncolytic treatment for gliomas. However, overcoming drug resistance mechanisms and limited blood-brain barrier (BBB) permeability are the remaining daunting issues. Latest research explores novel kinase inhibitors, yielding several promising results, including those from CK2 inhibition studies, as well as the possibility of relabelling the inhibitors previously approved for tumours other than glial tumours.
引用
收藏
页码:287 / 298
页数:12
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