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Dual function of ERRα in breast cancer and bone metastasis formation: implication of VEGF and osteoprotegerin.

Authors :
Fradet A
Sorel H
Bouazza L
Goehrig D
Dépalle B
Bellahcène A
Castronovo V
Follet H
Descotes F
Aubin JE
Clézardin P
Bonnelye E
Source :
Cancer research [Cancer Res] 2011 Sep 01; Vol. 71 (17), pp. 5728-38. Date of Electronic Publication: 2011 Jul 06.
Publication Year :
2011

Abstract

Bone metastasis is a complication occurring in up to 70% of advanced breast cancer patients. The estrogen receptor-related receptor alpha (ERRα) has been implicated in breast cancer and bone development, prompting us to examine whether ERRα may function in promoting the osteolytic growth of breast cancer cells in bone. In a mouse xenograft model of metastatic human breast cancer, overexpression of wild-type ERRα reduced metastasis, whereas overexpression of a dominant negative mutant promoted metastasis. Osteoclasts were directly affected and ERRα upregulated the osteoclastogenesis inhibitor, osteoprotegerin (OPG), providing a direct mechanistic basis for understanding how ERRα reduced breast cancer cell growth in bone. In contrast, ERRα overexpression increased breast cancer cell growth in the mammary gland. ERRα-overexpressing primary tumors were highly vascularized, consistent with an observed upregulation of angiogenic growth factor, the VEGF. In support of these findings, we documented that elevated expression of ERRα mRNA in breast carcinomas was associated with high expression of OPG and VEGF and with disease progression. In conclusion, our results show that ERRα plays a dual role in breast cancer progression in promoting the local growth of tumor cells, but decreasing metastatic growth of osteolytic lesions in bone.<br /> (©2011 AACR.)

Details

Language :
English
ISSN :
1538-7445
Volume :
71
Issue :
17
Database :
MEDLINE
Journal :
Cancer research
Publication Type :
Academic Journal
Accession number :
21734015
Full Text :
https://doi.org/10.1158/0008-5472.CAN-11-1431