PLoS ONE · 2013 · 68 citations · 39 references
MedicineCell BiologyOncologyMolecular OncologyNeoplasiaStem Cell BiologyCancer ProgressionCancer Stem Cell BiologyCancer Stem Cell NicheCancer Stem CellsMalignant NeoplasmsStem Cell TumorigenicityCancer Stem Cell BiomarkersCancer Stem Cell IdentificationCancer Stem Cell MarkersCancer Stem Cell NichesCancer Stem-like CellsMatrix MetalloproteinasesPerivascular Stem Cell NicheTumor Stem Cell Differentiation
Cancer stem cells contribute to the malignant phenotypes of a variety of cancers, but markers to identify human hypopharyngeal cancer (HPC) stem cells remain poorly understood. Here, we report that the CD271(+) population sorted from xenotransplanted HPCs possesses an enhanced tumor-initiating capability in immunodeficient mice. Tumors generated from the CD271(+) cells contained both CD271(+) and CD271(-) cells, indicating that the population could undergo differentiation. Immunohistological analyses of the tumors revealed that the CD271(+) cells localized to a perivascular niche near CD34(+) vasculature, to invasive fronts, and to the basal layer. In accordance with these characteristics, a stemness marker, Nanog, and matrix metalloproteinases (MMPs), which are implicated in cancer invasion, were significantly up-regulated in the CD271(+) compared to the CD271 (-) cell population. Furthermore, using primary HPC specimens, we demonstrated that high CD271 expression was correlated with a poor prognosis for patients. Taken together, our findings indicate that CD271 is a novel marker for HPC stem-like cells and for HPC prognosis.
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