In order to further assess the role of endogenous neurotensin on midbrain dopaminergic neuronal function, the effects of the selective neurotensin receptor antagonists SR 48692 and SR 48527 were investigated on the number of spontaneously active A9 and A10 dopaminergic neurons in rats. Single intrap
Involvement of the neurotensin receptor subtype NTR3 in the growth effect of neurotensin on cancer cell lines
✍ Scribed by Claude Dal Farra; Philippe Sarret; Valérie Navarro; Jean-Marie Botto; Jean Mazella; Jean-Pierre Vincent
- Book ID
- 102268720
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- French
- Weight
- 134 KB
- Volume
- 92
- Category
- Article
- ISSN
- 0020-7136
- DOI
- 10.1002/ijc.1225
No coin nor oath required. For personal study only.
✦ Synopsis
The expression of the 3 currently known neurotensin receptors was studied in human cancer cells of prostatic, colonic or pancreatic origin by means of RT-PCR analysis and binding experiments. All the cells selected for this work have been shown to exhibit a growth response to neurotensin. We found that the 7 transmembrane domain, levocabastine insensitive receptor (NTR1) is expressed in most but not all of the cells studied whereas the 7 transmembrane domain, levocabastine sensitive receptor (NTR2) is present in none of these cells. The 100 kDa-type I neurotensin receptor (NTR3) is expressed in all the cells assayed. Moreover, we demonstrated that neurotensin can stimulate the growth of CHO cells stably transfected with the NTR3. Taken together, our results strongly suggest that the NTR3 subtype could be involved in the growth response of human cancer cells to neurotensin.
📜 SIMILAR VOLUMES