| Literature DB >> 25016057 |
Hoon Ryu1, Ji-Eun Oh2, Ki-Jong Rhee3, Soon Koo Baik4, Jiye Kim5, Seong Joon Kang1, Joon Hyung Sohn6, Eunhee Choi6, Ha Cheol Shin7, Yong Man Kim7, Hyun Soo Kim7, Keum Seok Bae8, Young Woo Eom9.
Abstract
Although it has been reported that mesenchymal stem cells (MSCs) suppress tumor growth in vitro and in vivo, little is known about the underlying molecular mechanisms. We found that type I interferon is expressed in adipose tissue-derived stem cells (ASCs) cultured at high density, and ASCs and their conditioned medium (ASC-CM) suppress the growth of MCF-7 cells in vitro. Growth inhibition was amplified by glucose deprivation that resulted from high density culture of ASCs after 3days. The cytotoxic effect of the ASC-CM obtained from high density culture of ASCs was neutralized by anti-IFN-β antibody. STAT1 was phosphorylated in MCF-7 cells treated with ASC-CM, and JAK1/JAK2 inhibitor treatment decreased STAT1 phosphorylation. The cytotoxic effect of ASC-CM was reduced especially by JAK1 inhibitors in MCF-7 cells. Our findings suggest that ASCs cultured at high density express type I interferons, which suppresses tumor growth via STAT1 activation resulting from IFN-β secretion in MCF-7 breast cancer cells.Entities:
Keywords: Adipose tissue-derived stem cells; Growth suppression; High density culture; IFN-β; MCF-7
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Year: 2014 PMID: 25016057 DOI: 10.1016/j.canlet.2014.06.018
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679