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Get Free AccessInterestingly, elevated levels of endogenous GAS6 were identified in putative cancer stem cells (CSCs, CD133+/CD44+) compared to non-CSCs (CD133-/CD44-) isolated from PCa/osteoblast cocultures in vitro and in DTCs isolated from the bone marrow 24 hours after intracardiac injection. Moreover, we found that endogenous GAS6 expression is associated with Mer receptor expression in growth arrested (G1) PCa cells, which correlates with the increase of the CSC populations. Importantly, we found that overexpression of GAS6 activates phosphorylation of Mer receptor signaling and subsequent induction of the CSC phenotype in vitro and in vivo.Together these data suggest that endogenous GAS6 and Mer receptor signaling contribute to the establishment of PCa CSCs in the bone marrow microenvironment, which may have important implications for targeting metastatic disease.
Younghun Jung, Ann M. Decker, Jingcheng Wang, Eunsohl Lee, Lulia A. Kana, Kenji Yumoto, Frank C. Cackowski, James A. Van Rhee, Peter Carmeliet, Laura Buttitta, Todd M. Morgan, Russell S. Taichman (2016). Endogenous GAS6 and Mer receptor signaling regulate prostate cancer stem cells in bone marrow. , 7(18), DOI: https://doi.org/10.18632/oncotarget.8365.
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Type
Article
Year
2016
Authors
12
Datasets
0
Total Files
0
Language
en
DOI
https://doi.org/10.18632/oncotarget.8365
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