TY - JOUR
T1 - Antiproliferative effect of the C-terminal fragments of parathyroid hormone-related protein, PTHrP-(107-111) and (107-139), on osteoblastic osteosarcoma cells
AU - Valín, Alvaro
AU - García-Ocaña, Adolfo
AU - De Miguel, Fernando
AU - Sarasa, José L.
AU - Esbrit, Pedro
PY - 1997/2
Y1 - 1997/2
N2 - The C-terminal region of parathyroid hormone-related protein (PTHrP) containing the sequence (707-111) appears to be a potent inhibitor of osteoclastic bone resorption. In the present study, we have investigated the effect of human (h)PTHrP (107-139) and hPTHrP (107-111)NH2 on the proliferation of osteoblastic rat osteosarcoma UMR 106 cells. We found that both C-terminal PTHrP peptides, like hPTHrP (1-141), were antimitogenic for these cells, between 1 pM and 10 nM. [Tyr34]hPTHrP (1-34)NH2 was as potent as these peptides but less effective as growth inhibitor in these cells. UMR 106 cells were found to produce and secrete immunoreactive PTHrP. Addition of anti-PTHrP neutralizing antibodies to C- and N-terminal epitopes of PTHrP increased the growth of these cells. Our data suggest that the antiproliferative effect of these C-terminal PTHrP analogs may be independent of cyclic adenosine 3':5'-monophosphate (cAMP) and mediated by protein kinase C. These findings support an autocrine role of PTHrP in bone metabolism.
AB - The C-terminal region of parathyroid hormone-related protein (PTHrP) containing the sequence (707-111) appears to be a potent inhibitor of osteoclastic bone resorption. In the present study, we have investigated the effect of human (h)PTHrP (107-139) and hPTHrP (107-111)NH2 on the proliferation of osteoblastic rat osteosarcoma UMR 106 cells. We found that both C-terminal PTHrP peptides, like hPTHrP (1-141), were antimitogenic for these cells, between 1 pM and 10 nM. [Tyr34]hPTHrP (1-34)NH2 was as potent as these peptides but less effective as growth inhibitor in these cells. UMR 106 cells were found to produce and secrete immunoreactive PTHrP. Addition of anti-PTHrP neutralizing antibodies to C- and N-terminal epitopes of PTHrP increased the growth of these cells. Our data suggest that the antiproliferative effect of these C-terminal PTHrP analogs may be independent of cyclic adenosine 3':5'-monophosphate (cAMP) and mediated by protein kinase C. These findings support an autocrine role of PTHrP in bone metabolism.
UR - https://www.scopus.com/pages/publications/1842372716
U2 - 10.1002/(SICI)1097-4652(199702)170:2<209::AID-JCP13>3.0.CO;2-C
DO - 10.1002/(SICI)1097-4652(199702)170:2<209::AID-JCP13>3.0.CO;2-C
M3 - Article
C2 - 9009150
AN - SCOPUS:1842372716
SN - 0021-9541
VL - 170
SP - 209
EP - 215
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
IS - 2
ER -