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BMP4 inhibits breast cancer metastasis by blocking myeloid-derived suppressor cell activity.
Cao, Yuan; Slaney, Clare Y; Bidwell, Bradley N; Parker, Belinda S; Johnstone, Cameron N; Rautela, Jai; Eckhardt, Bedrich L; Anderson, Robin L.
Afiliación
  • Cao Y; Research Division, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia.
  • Slaney CY; Research Division, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia.
  • Bidwell BN; Research Division, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia.
  • Parker BS; Department of Biochemistry, La Trobe Institute for Molecular Science, La Trobe University, Melbourne, Australia.
  • Johnstone CN; Research Division, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia. Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Victoria, Australia. Department of Pharmacology, The University of Melbourne, Parkville, Victoria, Australia.
  • Rautela J; Research Division, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia. Department of Biochemistry, The University of Melbourne, Parkville, Victoria, Australia.
  • Eckhardt BL; Morgan Welch Inflammatory Breast Cancer Research and Clinic, Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas. robin.anderson@petermac.org beckhardt@mdanderson.org.
  • Anderson RL; Research Division, Peter MacCallum Cancer Centre, East Melbourne, Victoria, Australia. Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Victoria, Australia. Department of Pathology, The University of Melbourne, Parkville, Victoria, Australia. robin.anderson@peterma
Cancer Res ; 74(18): 5091-102, 2014 Sep 15.
Article en En | MEDLINE | ID: mdl-25224959
ABSTRACT
The TGFß growth factor family member BMP4 is a potent suppressor of breast cancer metastasis. In the mouse, the development of highly metastatic mammary tumors is associated with an accumulation of myeloid-derived suppressor cells (MDSC), the numbers of which are reduced by exogenous BMP4 expression. MDSCs are undetectable in naïve mice but can be induced by treatment with granulocyte colony-stimulating factor (G-CSF/Csf3) or by secretion of G-CSF from the tumor. Both tumor-induced and G-CSF-induced MDSCs effectively suppress T-cell activation and proliferation, leading to metastatic enhancement. BMP4 reduces the expression and secretion of G-CSF by inhibiting NF-κB (Nfkb1) activity in human and mouse tumor lines. Because MDSCs correlate with poor prognosis in patients with breast cancer, therapies based on activation of BMP4 signaling may offer a novel treatment strategy for breast cancer. Cancer Res; 74(18); 5091-102. ©2014 AACR.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Células Mieloides / Proteína Morfogenética Ósea 4 / Neoplasias Mamarias Experimentales Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans Idioma: En Revista: Cancer Res Año: 2014 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Células Mieloides / Proteína Morfogenética Ósea 4 / Neoplasias Mamarias Experimentales Tipo de estudio: Prognostic_studies Límite: Animals / Female / Humans Idioma: En Revista: Cancer Res Año: 2014 Tipo del documento: Article País de afiliación: Australia