The role of sialomucin CD164 (MGC-24v or endolyn) in prostate cancer metastasis

<p>Abstract</p> <p>Background</p> <p>The chemokine stromal derived factor-1 (SDF-1 or CXCL12) and its receptor CXCR4 have been demonstrated to be crucial for the homing of stem cells and prostate cancers to the marrow. While screening prostate cancers for CXCL12-respons...

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Main Authors: Bühring HJ, Shah RB, Wang J, Sun YX, Jung Y, Havens AM, Pienta KJ, Taichman RS
Format: Article
Language:English
Published: BMC 2006-07-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/6/195
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spelling doaj-ca26b8cc03a54f10bb2f6ca53014d6592020-11-24T21:14:33ZengBMCBMC Cancer1471-24072006-07-016119510.1186/1471-2407-6-195The role of sialomucin CD164 (MGC-24v or endolyn) in prostate cancer metastasisBühring HJShah RBWang JSun YXJung YHavens AMPienta KJTaichman RS<p>Abstract</p> <p>Background</p> <p>The chemokine stromal derived factor-1 (SDF-1 or CXCL12) and its receptor CXCR4 have been demonstrated to be crucial for the homing of stem cells and prostate cancers to the marrow. While screening prostate cancers for CXCL12-responsive adhesion molecules, we identified CD164 (MGC-24) as a potential regulator of homing. CD164 is known to function as a receptor that regulates stem cell localization to the bone marrow.</p> <p>Results</p> <p>Using prostate cancer cell lines, it was demonstrated that CXCL12 induced both the expression of CD164 mRNA and protein. Functional studies demonstrated that blocking CD164 on prostate cancer cell lines reduced the ability of these cells to adhere to human bone marrow endothelial cells, and invade into extracellular matrices. Human tissue microarrays stained for CD164 demonstrated a positive correlation with prostate-specific antigen levels, while its expression was negatively correlated with the expression of androgen receptor.</p> <p>Conclusion</p> <p>Our findings suggest that CD164 may participate in the localization of prostate cancer cells to the marrow and is further evidence that tumor metastasis and hematopoietic stem cell trafficking may involve similar processes.</p> http://www.biomedcentral.com/1471-2407/6/195
collection DOAJ
language English
format Article
sources DOAJ
author Bühring HJ
Shah RB
Wang J
Sun YX
Jung Y
Havens AM
Pienta KJ
Taichman RS
spellingShingle Bühring HJ
Shah RB
Wang J
Sun YX
Jung Y
Havens AM
Pienta KJ
Taichman RS
The role of sialomucin CD164 (MGC-24v or endolyn) in prostate cancer metastasis
BMC Cancer
author_facet Bühring HJ
Shah RB
Wang J
Sun YX
Jung Y
Havens AM
Pienta KJ
Taichman RS
author_sort Bühring HJ
title The role of sialomucin CD164 (MGC-24v or endolyn) in prostate cancer metastasis
title_short The role of sialomucin CD164 (MGC-24v or endolyn) in prostate cancer metastasis
title_full The role of sialomucin CD164 (MGC-24v or endolyn) in prostate cancer metastasis
title_fullStr The role of sialomucin CD164 (MGC-24v or endolyn) in prostate cancer metastasis
title_full_unstemmed The role of sialomucin CD164 (MGC-24v or endolyn) in prostate cancer metastasis
title_sort role of sialomucin cd164 (mgc-24v or endolyn) in prostate cancer metastasis
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2006-07-01
description <p>Abstract</p> <p>Background</p> <p>The chemokine stromal derived factor-1 (SDF-1 or CXCL12) and its receptor CXCR4 have been demonstrated to be crucial for the homing of stem cells and prostate cancers to the marrow. While screening prostate cancers for CXCL12-responsive adhesion molecules, we identified CD164 (MGC-24) as a potential regulator of homing. CD164 is known to function as a receptor that regulates stem cell localization to the bone marrow.</p> <p>Results</p> <p>Using prostate cancer cell lines, it was demonstrated that CXCL12 induced both the expression of CD164 mRNA and protein. Functional studies demonstrated that blocking CD164 on prostate cancer cell lines reduced the ability of these cells to adhere to human bone marrow endothelial cells, and invade into extracellular matrices. Human tissue microarrays stained for CD164 demonstrated a positive correlation with prostate-specific antigen levels, while its expression was negatively correlated with the expression of androgen receptor.</p> <p>Conclusion</p> <p>Our findings suggest that CD164 may participate in the localization of prostate cancer cells to the marrow and is further evidence that tumor metastasis and hematopoietic stem cell trafficking may involve similar processes.</p>
url http://www.biomedcentral.com/1471-2407/6/195
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