CD271 Defines a Stem Cell-Like Population in Hypopharyngeal Cancer
Author(s) -
Takayuki Imai,
Keiichi Tamai,
Sayuri Oizumi,
Kyoko Oyama,
Kazunori Yamaguchi,
Ikuro Sato,
Kennichi Satoh,
Kazuto Matsuura,
Shigeru Saijo,
Kazuo Sugamura,
Nobuyuki Tanaka
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0062002
Subject(s) - cancer stem cell , homeobox protein nanog , biology , stem cell , cancer research , cd34 , population , low affinity nerve growth factor receptor , pathology , stem cell marker , cancer , microbiology and biotechnology , embryonic stem cell , induced pluripotent stem cell , medicine , genetics , receptor , environmental health , gene , neurotrophin
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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