Author/Authors :
Ryu، نويسنده , , Hoon and Oh، نويسنده , , Ji-Eun and Rhee، نويسنده , , Ki-Jong and Baik، نويسنده , , Soon Koo and Kim، نويسنده , , Jiye and Kang، نويسنده , , Seong Joon and Sohn، نويسنده , , Joon Hyung and Choi، نويسنده , , Eunhee and Shin، نويسنده , , Ha Cheol and Kim، نويسنده , , Yong Man and Kim، نويسنده , , Hyun Soo and Bae، نويسنده , , Keum Seok and Eom، نويسنده , , Young Woo، نويسنده ,
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 3 days. 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.
Keywords :
Growth suppression , Adipose tissue-derived stem cells , IFN-? , MCF-7 , High density culture