Molecular targeting of cell death signal transduction pathways in cancer

被引:8
作者
Petak, Istvan
Houghton, Janet A.
Kopper, Laszlo
机构
[1] Semmelweis Univ, Dept Pathol & Expt Canc Res 1st, Mol Therapy Lab, H-1085 Budapest, Hungary
[2] Semmelweis Univ, Cooperat Res Ctr, Rat Drug Design Lab, H-1085 Budapest, Hungary
[3] St Jude Childrens Res Hosp, Dept Hematol Oncol, Div Mol Therapeut, Memphis, TN 38105 USA
[4] Semmelweis Univ, Hungarian Acad Sci, Res Grp Mol Pathol, H-1085 Budapest, Hungary
关键词
cell death; apoptosis; cancer;
D O I
10.2174/157436206775269217
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Suppression of cell death (most often apoptosis) by survival signals, or by defects in cell death signal transduction pathways, is considered one of the obligate hallmarks of malignant transformation. However, molecular survival strategies to evade cell death only have relevance in the presence of pro-death signals. Discovery of the apoptotic properties of oncogenes responsible for increased tumor cell proliferation (e.g. c-Myc) provided the most important example for such signals and led to the concept of synthetic lethal targeting as a strategy of identifying cancer specific drug target molecules. Besides growth signal autonomy, other hallmarks of oncogenesis (insensitivity to anti-growth signals, limitless replicative potential, invasion and metastasis, angiogenesis and increased genomic instability) are also challenged by increased susceptibility to various forms of cell death. Therefore, cancer cells must acquire survival strategies to suppress these cell death/apoptosis mechanisms. Novel signal transduction therapies can target molecules involved in these strategies to trigger tumor specific cell death.
引用
收藏
页码:113 / 131
页数:19
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