Abstract
Human amniotic membrane-derived stromal cells (hAMSC) are candidates for cell-based therapies. We examined the characteristics of hAMSC including the interaction between hAMSC and breast cancer cells, MCF-7, and MDA-MB-231. Human amniotic membrane-derived stromal cells showed typical MSC properties, including fibroblast-like morphology, surface antigen expression, and mesodermal differentiation. To investigate cell-cell interaction via secreted molecules, we cultured breast cancer cells in hAMSC-conditioned medium (hAMSC-CM) and analyzed their proliferation, migration, and secretome profiles. MCF-7 and MDA-MB-231 cells exposed to hAMSC-CM showed increased proliferation and migration. However, in hAMSC-CM, MCF-7 cells proliferated significantly faster than MDA-MB-231 cells. When cultured in hAMSC-CM, MCF-7 cells migrated faster than MDA-MB-231 cells. Two cell types showed different profiles of secreted factors. MCF-7 cells expressed much amounts of IL-8, GRO, and MCP-1 in hAMSC-CM. Human amniotic membrane-derived stromal cells interact with breast cancer cells through secreted molecules. Factors secreted by hAMSCs promote the proliferation and migration of MCF-7 breast cancer cells. For much safe cell-based therapies using hAMSC, it is necessary to study carefully about interaction between hAMSC and cancer cells.
Original language | English |
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Pages (from-to) | 10-16 |
Number of pages | 7 |
Journal | Tissue and Cell |
Volume | 47 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2015 Feb 1 |
Bibliographical note
Funding Information:This work was supported by a grant ( 12171MFDS311 ) from Ministry of Food and Drug Safety in 2012.
Publisher Copyright:
© 2014 Elsevier Ltd.
Keywords
- Amniotic membrane
- MCF-7
- MDA-MB-231
- Secretion
ASJC Scopus subject areas
- Developmental Biology
- Cell Biology