The dynamic yin-yang interaction of CXCR4 and CXCR7 in breast cancer metastasis

The contribution of CXCR7 to the tumor microenvironment has introduced a new level of complexity to CXCL12 signaling in breast cancer. In the previous issue of Breast Cancer Research, Hernandez and colleagues delineate the roles of CXCR4 and CXCR7 in tumor invasion and metastasis. The authors demons...

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Published inBreast cancer research : BCR Vol. 14; no. 1; p. 103
Main Authors Hawkins, Oriana E, Richmond, Ann
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 26.01.2012
BioMed Central
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Abstract The contribution of CXCR7 to the tumor microenvironment has introduced a new level of complexity to CXCL12 signaling in breast cancer. In the previous issue of Breast Cancer Research, Hernandez and colleagues delineate the roles of CXCR4 and CXCR7 in tumor invasion and metastasis. The authors demonstrate that co-expression of CXCR7 and CXCR4 results in inhibition of CXCL12-mediated invasion, reduced intravasation of tumor cells into the vasculature, and fewer lung metastases compared with parental tumors. The results of this study suggest the combination of small molecule inhibitors of CXCR4 and CXCR7 could dramatically reduce invasion, intravasation, and metastasis and could be highly beneficial for the treatment of invasive breast cancer.
AbstractList The contribution of CXCR7 to the tumor microenvironment has introduced a new level of complexity to CXCL12 signaling in breast cancer. In the previous issue of Breast Cancer Research, Hernandez and colleagues delineate the roles of CXCR4 and CXCR7 in tumor invasion and metastasis. The authors demonstrate that co-expression of CXCR7 and CXCR4 results in inhibition of CXCL12-mediated invasion, reduced intravasation of tumor cells into the vasculature, and fewer lung metastases compared with parental tumors. The results of this study suggest the combination of small molecule inhibitors of CXCR4 and CXCR7 could dramatically reduce invasion, intravasation, and metastasis and could be highly beneficial for the treatment of invasive breast cancer.
The contribution of CXCR7 to the tumor microenvironment has introduced a new level of complexity to CXCL12 signaling in breast cancer. In the previous issue of Breast Cancer Research , Hernandez and colleagues delineate the roles of CXCR4 and CXCR7 in tumor invasion and metastasis. The authors demonstrate that co-expression of CXCR7 and CXCR4 results in inhibition of CXCL12-mediated invasion, reduced intravasation of tumor cells into the vasculature, and fewer lung metastases compared with parental tumors. The results of this study suggest the combination of small molecule inhibitors of CXCR4 and CXCR7 could dramatically reduce invasion, intravasation, and metastasis and could be highly beneficial for the treatment of invasive breast cancer.
ArticleNumber 103
Audience Academic
Author Richmond, Ann
Hawkins, Oriana E
AuthorAffiliation 1 Department of Cancer Biology, Vanderbilt University School of Medicine, US Department of Veterans Affairs, 2220 Pierce Avenue, 771 Preston Research Building, Nashville, TN 37232-6840, USA
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SubjectTerms Animals
Breast cancer
Breast Neoplasms - metabolism
Breast Neoplasms - pathology
Cancer metastasis
Comparative analysis
Female
Humans
Parenting
Receptors, CXCR - metabolism
Receptors, CXCR4 - metabolism
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Title The dynamic yin-yang interaction of CXCR4 and CXCR7 in breast cancer metastasis
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