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Involvement of chemokine receptors in breast cancer metastasis.
- Source :
-
Nature [Nature] 2001 Mar 01; Vol. 410 (6824), pp. 50-6. - Publication Year :
- 2001
-
Abstract
- Breast cancer is characterized by a distinct metastatic pattern involving the regional lymph nodes, bone marrow, lung and liver. Tumour cell migration and metastasis share many similarities with leukocyte trafficking, which is critically regulated by chemokines and their receptors. Here we report that the chemokine receptors CXCR4 and CCR7 are highly expressed in human breast cancer cells, malignant breast tumours and metastases. Their respective ligands CXCL12/SDF-1alpha and CCL21/6Ckine exhibit peak levels of expression in organs representing the first destinations of breast cancer metastasis. In breast cancer cells, signalling through CXCR4 or CCR7 mediates actin polymerization and pseudopodia formation, and subsequently induces chemotactic and invasive responses. In vivo, neutralizing the interactions of CXCL12/CXCR4 significantly impairs metastasis of breast cancer cells to regional lymph nodes and lung. Malignant melanoma, which has a similar metastatic pattern as breast cancer but also a high incidence of skin metastases, shows high expression levels of CCR10 in addition to CXCR4 and CCR7. Our findings indicate that chemokines and their receptors have a critical role in determining the metastatic destination of tumour cells.
- Subjects :
- Actins metabolism
Animals
Blood Proteins metabolism
Chemokine CXCL12
Chemotaxis
Humans
Lung pathology
Lymphatic Metastasis
Mice
Mice, SCID
Neoplasm Invasiveness
Neoplasm Transplantation
Receptors, CCR7
Receptors, CXCR4 antagonists & inhibitors
Tumor Cells, Cultured
Breast Neoplasms pathology
Chemokines, CXC metabolism
Neoplasm Metastasis
Receptors, CXCR4 metabolism
Receptors, Chemokine metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0028-0836
- Volume :
- 410
- Issue :
- 6824
- Database :
- MEDLINE
- Journal :
- Nature
- Publication Type :
- Academic Journal
- Accession number :
- 11242036
- Full Text :
- https://doi.org/10.1038/35065016