Cell death signalling pathways in the pathogenesis and therapy of haematologic malignancies: Overview of therapeutic approaches

被引:1
作者
Klener, P., Jr.
Andera, L.
Klener, P.
Necas, E.
Zivny, J.
机构
[1] Charles Univ Prague, Dept Pathophysiol, Fac Med 1, Prague 12853, Czech Republic
[2] Charles Univ Prague, Ctr Expt Hematol, Fac Med 1, Prague 12853, Czech Republic
[3] Acad Sci Czech Republ, Inst Genet Mol, Lab Cell Signalling & Apoptosis, Prague, Czech Republic
[4] Charles Univ Prague, Dept Med 1, Fac Med 1, Dept Clin Hematol, Prague 12853, Czech Republic
[5] Inst Hematol & Blood Transfus, Prague, Czech Republic
关键词
leukaemia; lymphoma; apoptosis; TNF-related apoptosis inducing ligand; Bcl-2 protein family; inhibitor of apoptosis proteins (IAPs); heat-shock proteins (HSPs); heat-shock protein inhibitors (HSPI); JAK; STAT; Bcr-Ab1; receptor tyrosine kinase; mitogen-activated protein kinase (MAPK); phosphatidylinositol 3 kinase (PI3K); Akt/protein kinase B; mammalian target of rapamycin (mTOR); NF kappa B; cyclin-dependent kinases (CDKs); cyclin-dependent kinase inhibitors (CDKI); histone deacetylase inhibitors (HDACI); iron chelators;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Malignant diseases, including haematologic malignancies, are associated with defects in the cell death mechanism. These defects are not only important for the growth advantage of the malignant clone, but when understood can be used for specific therapeutic targeting of malignant cells while sparing normal cells. The promising groups of agents that trigger, directly or indirectly, apoptosis of haematologic cancer cells are reviewed in this article. Some of the agents have recently been approved for therapy, some are under the clinical evaluation in various phases of clinical trials and some are tested under the experimental laboratory conditions.
引用
收藏
页码:119 / 136
页数:18
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