Epithelial expression of the 75-kDa low-affinity neurotrophin receptor (p75 NTR ) is inversely associated with the malignant progression of the human prostate. To elucidate the function of p75 NTR in the prostate, the human prostate epithelial tumor cell line TSU-pr1, which does not express p75 NTR
NGF induces apoptosis in a human neuroblastoma cell line expressing the neurotrophin receptor p75NTR
β Scribed by P. Kuner; C. Hertel
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 162 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0360-4012
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β¦ Synopsis
Nerve growth factor (NGF) has been demonstrated to support survival and differentiation of neuronal cells. Recently, a role of NGF in neuronal apoptosis has been suggested. NGF binds to tropomyosin receptor kinase A (TrkA) and to 75-kDa NGF receptor (p75 NTR ). TrkA is responsible for differentiation and survival, but p75 NTR , a member of the death receptor family, seems to mediate the apoptotic effect of NGF. Here we demonstrate that NGF-but not neurotrophin-3 (NT-3) or brain-derived neurotrophic factor (BDNF)induced apoptosis in p75 NTR -expressing human neuroblastoma SK-N-MC cells. BDNF prevented NGFinduced apoptosis. NGF-induced apoptosis was accompanied by the release of NFB p65 and the activation of stress-activated protein kinase/c-jun amino terminal kinase. Because p75 NTR and NGF are upregulated in Alzheimer's disease, NGF/p75 NTR might be involved in neuronal cell death related to the disease.
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BACKGROUND. We analyzed the cytotoxic properties of the new heterodinucleoside phosphate dimer 5-FdU-NOAC, which is composed of the cytotoxic drugs 5-FdU and N 4octadecyl-1-β€-D-arabinofuranosylcytosine (NOAC) against human prostate tumor cells. METHODS. 5-FdU-NOAC effects on cell proliferation, cell