| Literature DB >> 24797826 |
Tegy J Vadakkan1, John D Landua2, Wen Bu2, Wei Wei2, Fuhai Li2, Stephen T C Wong2, Mary E Dickinson2, Jeffrey M Rosen2, Michael T Lewis2, Mei Zhang1.
Abstract
Cancer stem cells (CSCs, or tumor-initiating cells) may be responsible for tumor formation in many types of cancer, including breast cancer. Using high-resolution imaging techniques, we analyzed the relationship between a Wnt-responsive, CSC-enriched population and the tumor vasculature using p53-null mouse mammary tumors transduced with a lentiviral Wnt signaling reporter. Consistent with their localization in the normal mammary gland, Wnt-responsive cells in tumors were enriched in the basal/myoepithelial population and generally located in close proximity to blood vessels. The Wnt-responsive CSCs did not colocalize with the hypoxia-inducible factor 1α-positive cells in these p53-null basal-like tumors. Average vessel diameter and vessel tortuosity were increased in p53-null mouse tumors, as well as in a human tumor xenograft as compared with the normal mammary gland. The combined strategy of monitoring the fluorescently labeled CSCs and vasculature using high-resolution imaging techniques provides a unique opportunity to study the CSC and its surrounding vasculature. ©AlphaMed Press.Entities:
Keywords: Cancer stem cells; In vivo optical imaging; Microvasculature; Signal transduction; Stem cell microenvironment; p53
Mesh:
Substances:
Year: 2014 PMID: 24797826 PMCID: PMC4073819 DOI: 10.5966/sctm.2013-0088
Source DB: PubMed Journal: Stem Cells Transl Med ISSN: 2157-6564 Impact factor: 6.940