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Adipose Tissue-Derived Stem Cells Differentiate into Carcinoma-Associated Fibroblast-Like Cells under the Influence of Tumor-Derived Factors
- Source :
- Analytical Cellular Pathology, Vol 33, Iss 2, Pp 61-79 (2010)
- Publication Year :
- 2010
- Publisher :
- Wiley, 2010.
-
Abstract
- Carcinoma-associated fibroblasts (CAF) are considered to contribute to tumor growth, invasion and metastasis. However, the cell type of origin remains unknown. Since human adipose tissue-derived stem cells (hASCs) are locally adjacent to breast cancer cells and might directly interact with tumor cells, we investigated whether CAFs may originate from hASCs. We demonstrated that a significant percentage of hASCs differentiated into a CAF-like myofibroblastic phenotype (e.g., expression of alpha smooth muscle actin and tenascin-C) when exposed to conditioned medium from the human breast cancer lines MDAMB231 and MCF7. The conditioned medium from MDAMB231 and MCF7 contains significant amounts of transforming growth factor-beta 1 (TGFβ1) and the differentiation of hASCs towards CAFs is dependent on TGFβ1 signaling via Smad3 in hASCs. The induction of CAFs can be abolished using a neutralizing antibody to TGFβ1 as well as by pretreatment of the hASCs with SB431542, a TGFβ1 receptor kinase inhibitor. Additionally, we found that these hASC-derived CAF-like cells exhibit functional properties of CAFs, including the ability to promote tumor cell invasion in an in vitro invasion assay, as well as increased expression of stromal-cell-derived factor 1 (SDF-1) and CCL5. Taken together, these data suggest that hASCs are a source of CAFs which play an important role in the tumor invasion.
Details
- Language :
- English
- ISSN :
- 22107177 and 22107185
- Volume :
- 33
- Issue :
- 2
- Database :
- Directory of Open Access Journals
- Journal :
- Analytical Cellular Pathology
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.0590896b78a40c48c42a93565475da3
- Document Type :
- article
- Full Text :
- https://doi.org/10.3233/ACP-CLO-2010-0535