Skip Navigation



Carcinogenesis Advance Access published online on January 30, 2009

Carcinogenesis, doi:10.1093/carcin/bgp036
This Article
Right arrow Advance Access manuscript (PDF)
Right arrow Supplementary Data
Right arrow All Versions of this Article:
30/4/589    most recent
bgp036v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Muehlberg, F.
Right arrow Articles by Alt, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Muehlberg, F.
Right arrow Articles by Alt, E.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2009. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Tissue resident stem cells promote breast cancer growth and metastasis.

Fabian Muehlberg1,a, Yao-Hua Song*,1,a, Alexander Krohn1, Severin Pinilla1, Lilly Droll1, Xiaohong Leng1, Max Seidensticker2, Jens Ricke2, Andrew Altman1, Eswaran Devarajan1, Weili Liu1, Ralph Arlinghaus1 and Eckhard Alt1,*

1 Department of Molecular Pathology, University of Texas M.D. Anderson Cancer Center, Houston, Texas 77030
2 Clinic for Diagnostic Radiology, University Hospital, Otto-von-Guericke University Magdeburg

* Correspondence authors: Eckhard Alt, M.D., Ph.D. or Yao-Hua Song, M.D., Ph.D., University of Texas, MD Anderson Cancer Center, SCRB2, Box 951, 7435 Fannin Street, Houston, TX 77054. ealt{at}mdanderson.org, ysong{at}mdanderson.org, 713-834-6106 (phone), 713-834-6105 (fax).

Mesenchymal stem cells derived from bone marrow have recently been described to localize to breast carcinomas and to integrate into the tumor-associated stroma. In the present study, we investigated whether adipose tissue derived stem cells (ASCs) could play a role in tumor growth and invasion. Compared to bone marrow derived cells, ASCs as tissue resident stem cells are locally adjacent to breast cancer cells and may interact with tumor cells directly. Here, we demonstrate that ASCs cause the cancer to grow significantly faster when added to a murine breast cancer 4T1 cell line. We further show that breast cancer cells enhance the secretion of stromal cell-derived factor -1 (SDF-1) from ASCs, which then acts in a paracrine fashion on the cancer cells to enhance their motility, invasion and metastasis. The tumor promoting effect of ASCs was abolished by knock down of the CXCR4 receptor in 4T1 tumor cells. We demonstrated that ASCs home to tumor site and promote tumor growth not only when co-injected locally but also when injected intravenously. Furthermore, we demonstrated that ASCs incorporate into tumor vessels and differentiate into endothelial cells. The tumor promoting effect of tissue resident stem cells was also tested and validated using a human breast cancer line MDA-MB-231 cells and human adipose tissue derived stem cells. Our findings indicate that the interaction of local tissue resident stem cells with tumor stem cells plays an important role in tumor growth and metastasis.

Key Words: stem cell • breast cancer • stroma • SDF-1 • angiogenesis • cancer stem cells • CXCR4 • recruitment


a These authors contributed equally to this work.

Received November 17, 2008; revised January 21, 2009; accepted January 24, 2009.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Cancer Res.Home page
Y. Zhang, A. Daquinag, D. O. Traktuev, F. Amaya-Manzanares, P. J. Simmons, K. L. March, R. Pasqualini, W. Arap, and M. G. Kolonin
White Adipose Tissue Cells Are Recruited by Experimental Tumors and Promote Cancer Progression in Mouse Models
Cancer Res., June 15, 2009; 69(12): 5259 - 5266.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.