Dissemination of cancer stem cells (CSCs) serves as the basis of metastasis. Recently, we demonstrated that circulating prostate cancer targets the hematopoietic stem cell (HSCs) ‘niche’ in marrow during dissemination. Once in the niche, disseminated tumor cells (DTCs) may remain dormant for extended periods. As the major function of the HSC niche is to maintain stem cell functions, we hypothesized that the niche regulates CSC activities of DTCs. Here we show that DTCs recovered from marrow were significantly enriched for a CSC phenotype. Critically, the conversion of DTCs to CSCs is regulated by niche-derived GAS6 through the Mer/mTOR; molecules previously shown to regulate dormancy. The data demonstrate that the niche plays a significant role in maintaining tumor-initiating prostate cancer in marrow and suggests a functional relationship between CSCs and dormancy. Understanding how the marrow niche regulates the conversion of DTCs to CSCs is critical for the development of therapeutics specifically targeting skeletal bone metastasis and dormancy.
[1]
D. Beebe,et al.
PDMS bonding by means of a portable, low-cost corona system.
,
2006,
Lab on a chip.
[2]
G. Whitesides.
The origins and the future of microfluidics
,
2006,
Nature.
[3]
G. Whitesides,et al.
Components for integrated poly(dimethylsiloxane) microfluidic systems
,
2002,
Electrophoresis.
[4]
G. Whitesides,et al.
Rapid Prototyping of Microfluidic Systems in Poly(dimethylsiloxane).
,
1998,
Analytical chemistry.