Polyamine biosynthesis as a target to inhibit apoptosis of non-tumoral cells

被引:28
作者
Flamigni, F.
Stanic, I.
Facchini, A.
Cetrullo, S.
Tantini, B.
Borzi, R. M.
Guarnieri, C.
Caldarera, C. M.
机构
[1] Univ Bologna, Dept Biochem G Moruzzi, I-40126 Bologna, Italy
[2] IOR, Ist Ric Codivilla Putti, Lab Immunol & Genet, Bologna, Italy
[3] Natl Inst Cardiovasc Res, Bologna, Italy
关键词
polyamines; apoptosis; signal transduction; difluoromethylornithine; caspases; non-tumoral cells;
D O I
10.1007/s00726-007-0514-3
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
Growing evidence suggests a role for polyamines in apoptosis, although the relationship appears to be complex. alpha-Difluoromethylornithine (DFMO), a largely used ornithine decarboxylase inhibitor, is cytostatic, hardly cytotoxic and may even increase the resistance of tumour cells to some apoptotic stimuli. This may represent a problem in cancer therapy, where the killing of tumoral cells would be a desired effect, but could be an advantage in other pathological contexts related to an excess of apoptosis, such as cardiovascular diseases, stem cell transplantation, arthritis and infections. In different cellular models, polyamine depletion following treatment with polyamine biosynthesis inhibitors appears to inhibit mitochondrial and death receptor pathways of apoptosis by affecting key proteins. These studies indicate that inhibition of polyamine biosynthesis may prevent or reduce the apoptotic response triggered by a variety of stimuli in non-tumoral cells, such as cardiac cells, stem cells, chondrocytes, macrophages and intestinal epithelial cells.
引用
收藏
页码:197 / 202
页数:6
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