Parathyroid hormone-related protein (PTHrP)-(1-139) isoform is efficiently secreted in vitro and enhances breast cancer metastasis to bone in vivo

• Published in: Bone (New York, N.Y.) N.Y.), 2002-05, Vol.30 (5), p.670-676
• Main Authors: Guise, T.A, Yin, J.J, Thomas, R.J, Dallas, M, Cui, Y, Gillespie, M.T
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Bone metastases; Bone Neoplasms - diagnostic imaging; Bone Neoplasms - secondary; Breast Neoplasms - metabolism; Breast Neoplasms - pathology; Calcium - blood; Diseases of the osteoarticular system; Female; Humans; Hypercalcemia; Hypercalcemia - metabolism; In Vitro Techniques; Medical sciences; Mice; Mice, Nude; Osteoclast; Osteoclasts - metabolism; Osteolysis; Osteolysis - metabolism; Osteosarcoma; Parathyroid Hormone - genetics; Parathyroid Hormone - metabolism; Parathyroid Hormone-Related Protein; Parathyroid hormone-related protein (PTHrP); Peptide Fragments - genetics; Peptide Fragments - metabolism; Protein Isoforms - genetics; Protein Isoforms - metabolism; Proteins - genetics; Proteins - metabolism; Radiography; Rats; Transfection; Tumor Cells, Cultured - metabolism; Tumor Cells, Cultured - transplantation; Tumors of striated muscle and skeleton
• ISSN: 8756-3282; 1873-2763
• DOI: 10.1016/S8756-3282(02)00685-3

Parathyroid hormone-related peptide (PTHrP) is a mediator of local osteolysis due to breast cancer. Three isoforms of PTHrP, (1-139), (1-141), and (1-173), are products of alternative splicing in humans, but the specific contribution of each of these isoforms to osteolytic metastasis caused by breast cancer has not been evaluated. To determine the role of PTHrP isoforms in breast cancer metastasis to bone, the human breast cancer cell line MDA-MB-231 (MDA-231) was stably transfected with cDNAs for human prepro PTHrP-(1-139), -(1-141), or -(1-173). Stable MDA/PTHrP-(1-139) clones expressed more PTHrP mRNA and secreted more PTHrP protein, compared with MDA/PTHrP-(1-141), -(1-173), or parental MDA-231. Parental MDA-231 cells and clones expressing each isoform had similar growth rates in vitro. In a mouse model of bone metastases, the osteolytic lesion area of radiographs was greatest in mice bearing MDA/PTHrP-(1-139) compared with those bearing MDA/PTHrP-(1-141), -(1-173), or parental MDA-231. Ca ++ and plasma PTHrP concentrations were significantly higher in the MDA/PTHrP-(1-139) compared with the MDA/PTHrP-(1-141), -(1-173), or parental MDA-231 groups. These data demonstrate that the PTHrP-(1-139) isoform was produced to a greater extent than PTHrP-(1-141) or -(1-173), and in vivo enhanced osteolysis with increased plasma PTHrP concentrations and hypercalcemia compared with overexpression of PTHrP-(1-141) or -(1-173).