Quantitative comparison of PTH1R in breast cancer MCF7 and osteosarcoma SaOS-2 cell lines

被引:7
作者
Alokail, Majed S. [1 ]
Peddie, Margaret J. [2 ]
机构
[1] King Saud Univ, Dept Biochem, Coll Sci 5, Riyadh 11451, Saudi Arabia
[2] Univ Southampton, Sch Biol Sci, Div Cell Sci, Southampton, Hants, England
关键词
PTH; PTHrP; PTH1; receptor; MCF7; cells; SaOS-2;
D O I
10.1002/cbf.1475
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
The aim of the present study was to compare the classical parathyroid hormone/parathyroid hormone-related peptide (PTH/PTHrP) receptors in MCF7 breast cancer cells with SaOS-2 osteosarcoma cell line. Quantitative binding showed that I-125-PTHrP-1-34(Tyr) binds with a single binding site in both cells. However I-125-PTHrP-1-34(Tyr) has higher affinity binding in MCF7 (K-D = 1.88 +/- 0.08 nM) than in SaOS-2 cells (K-D = 4.4 +/- 0.185 nM). The competitive binding using 3.3 nM I-125-PTHrP-1-34(Tyr) with increasing amounts (0.33-33 nM) of unlabelled human PTHrP-1-34, PTHrP-7-34, PTHrP-1-86 His(5)-PTHrP-1-36, His(5)-Phe(23)-PTHrP-1-36 or PTH-1-34 revealed different displacements. In SaOS-2 the PTHrP-7-34 and PTHrP-1-86 caused similar displacement compared with 73% by PTH-1-34 and 70% by PTHrP-1-34. However, in MCF7, PTHrP-7-34, PTHrP-1-86 and PTH-1-34 displaced by 54%, 72% and 67%, respectively, compared to 87% by PTHIP-1-34. The His(5)-Phe(23)-PTHrP-1-36 caused an increase in the KD from 2.0 +/- 0.03 nM to 2.75 +/- 0.045 nM in MCF7 cells, but had no significant effect in SaOS-2 cells. The PTH/PTHrP receptor in both cell lines revealed a single 85 KDa band with different intensity. Our results suggest that the PTH/PTHrP receptor in MCF7 cells has higher binding affinity for PTHrP than PTH compared to the receptor in SaOS-2 cells. Copyright (C) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:522 / 533
页数:12
相关论文
共 45 条
[1]   Characterisation of ligand binding to the parathyroid hormone/parathyroid hormone-related peptide receptor in MCF7 breast cancer cells and SaOS-2 osteosarcoma cells [J].
Alokail, Majed S. ;
Peddie, Margaret J. .
CELL BIOCHEMISTRY AND FUNCTION, 2007, 25 (02) :139-147
[2]  
Alokail MS, 2004, SAUDI MED J, V25, P615
[3]   Solution structure of parathyroid hormone related protein (residues 1-34) containing an Ala substituted for an Ile in position 15 (PTHrP[Ala(15)]-(1-34)) [J].
Barden, JA ;
Cuthbertson, RM ;
Wu, JZ ;
Moseley, JM ;
Kemp, BE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (47) :29572-29578
[4]   The human PTH2 receptor: Binding and signal transduction properties of the stably expressed recombinant receptor [J].
Behar, V ;
Pines, M ;
Nakamoto, C ;
Greenberg, Z ;
Bisello, A ;
Stueckle, SM ;
Bessalle, R ;
Usdin, TB ;
Chorev, M ;
Rosenblatt, M ;
Suva, LJ .
ENDOCRINOLOGY, 1996, 137 (07) :2748-2757
[5]   PARATHYROID-HORMONE (PTH)/PTH-RELATED PROTEIN (PTHRP) RECEPTOR EXPRESSION AND MITOGENIC RESPONSES IN HUMAN BREAST-CANCER CELL-LINES [J].
BIRCH, MA ;
CARRON, JA ;
SCOTT, M ;
FRASER, WD ;
GALLAGHER, JA .
BRITISH JOURNAL OF CANCER, 1995, 72 (01) :90-95
[6]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]   CLONED, STABLY EXPRESSED PARATHYROID-HORMONE (PTH)/PTH-RELATED PEPTIDE RECEPTORS ACTIVATE MULTIPLE MESSENGER SIGNALS AND BIOLOGICAL RESPONSES IN LLC-PK1 KIDNEY-CELLS [J].
BRINGHURST, FR ;
JUPPNER, H ;
GUO, J ;
URENA, P ;
POTTS, JT ;
KRONENBERG, HM ;
ABOUSAMRA, AB ;
SEGRE, GV .
ENDOCRINOLOGY, 1993, 132 (05) :2090-2098
[8]   Selective and nonselective inverse agonists for constitutively active type-1 parathyroid hormone receptors: Evidence for altered receptor conformations [J].
Carter, PH ;
Petroni, BD ;
Gensure, RC ;
Schipani, E ;
Potts, JT ;
Gardella, TJ .
ENDOCRINOLOGY, 2001, 142 (04) :1534-1545
[9]   EXPRESSION OF A PARATHYROID HORMONE-LIKE PROTEIN AND ITS RECEPTOR DURING DIFFERENTIATION OF EMBRYONAL CARCINOMA-CELLS [J].
CHAN, SDH ;
STREWLER, GJ ;
KING, KL ;
NISSENSON, RA .
MOLECULAR ENDOCRINOLOGY, 1990, 4 (04) :638-646
[10]   Parathyroid hormone-related protein and its receptors:: nuclear functions and roles in the renal and cardiovascular systems, the placental trophoblasts and the pancreatic islets [J].
Clemens, TL ;
Cormier, S ;
Eichinger, A ;
Endlich, K ;
Fiaschi-Taesch, N ;
Fischer, E ;
Friedman, PA ;
Karaplis, AC ;
Massfelder, T ;
Rossert, J ;
Schlüter, KD ;
Silve, C ;
Stewart, AF ;
Takane, K ;
Helwig, JJ .
BRITISH JOURNAL OF PHARMACOLOGY, 2001, 134 (06) :1113-1136