Side population rather than CD133<sup>+ </sup>cells distinguishes enriched tumorigenicity in hTERT-immortalized primary prostate cancer cells

<p>Abstract</p> <p>Background</p> <p>Subpopulations of cancer cells with the capacity of generating solid tumors have been characterized. In various cancer types, including prostate cancer cells, a side population (SP) and CD133-expressing cells have been proposed as co...

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Main Authors: Wolcott Karen, Cannon Virginetta, Wang Honghe, Zhou Jianjun, Song Hongbin, Yates Clayton
Format: Article
Language:English
Published: BMC 2011-09-01
Series:Molecular Cancer
Subjects:
Online Access:http://www.molecular-cancer.com/content/10/1/112
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author Wolcott Karen
Cannon Virginetta
Wang Honghe
Zhou Jianjun
Song Hongbin
Yates Clayton
author_facet Wolcott Karen
Cannon Virginetta
Wang Honghe
Zhou Jianjun
Song Hongbin
Yates Clayton
author_sort Wolcott Karen
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Subpopulations of cancer cells with the capacity of generating solid tumors have been characterized. In various cancer types, including prostate cancer cells, a side population (SP) and CD133-expressing cells have been proposed as containing a population cancer cells with stem-like ability. Therefore the aim of this work was to determine, in prostate cancer cell lines, the frequency and tumorigenic potential of SP and CD133+ cells.</p> <p>Results</p> <p><it>In vitro </it>2D colony-forming assay and sphere-forming assay, Flow cytometry analysis and magnetic cell sorting were utilized to sort CD133+, CD133- and Side population (SP) cells. Our findings indicate that CD44 and integrin α-6 are uniformly expressed in the hTERT cell lines; however, CD133 is expressed only in a small population (< 0.1%). FACS-sorted CD133+ and CD133- cells exhibited similar tumorigenicity <it>in vitro </it>and <it>in vivo</it>. Additionally, for the hTERT cells, SP rather than CD133 expression showed an 8-fold enhanced tumorigenic potential. The data suggest that SP cells, rather than those with CD133 marker, contain the rare population of CSC capable of producing prostate tumors.</p> <p>Conclusion</p> <p>Collectively, our data suggest that although CD133 is expressed only in a small population of hTERT-immortalized prostate cancer cells, it is not likely to be associated with stem cells, as CD133- and CD133+ cells exhibited similar tumorigenicity. However, SP isolated cells, appear to be enriched with tumorigenic stem-like cells capable of generating palpable tumors.</p>
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spelling doaj.art-63c3bb637a924145b0bc4d2c0bee5f202022-12-22T03:26:30ZengBMCMolecular Cancer1476-45982011-09-0110111210.1186/1476-4598-10-112Side population rather than CD133<sup>+ </sup>cells distinguishes enriched tumorigenicity in hTERT-immortalized primary prostate cancer cellsWolcott KarenCannon VirginettaWang HongheZhou JianjunSong HongbinYates Clayton<p>Abstract</p> <p>Background</p> <p>Subpopulations of cancer cells with the capacity of generating solid tumors have been characterized. In various cancer types, including prostate cancer cells, a side population (SP) and CD133-expressing cells have been proposed as containing a population cancer cells with stem-like ability. Therefore the aim of this work was to determine, in prostate cancer cell lines, the frequency and tumorigenic potential of SP and CD133+ cells.</p> <p>Results</p> <p><it>In vitro </it>2D colony-forming assay and sphere-forming assay, Flow cytometry analysis and magnetic cell sorting were utilized to sort CD133+, CD133- and Side population (SP) cells. Our findings indicate that CD44 and integrin α-6 are uniformly expressed in the hTERT cell lines; however, CD133 is expressed only in a small population (< 0.1%). FACS-sorted CD133+ and CD133- cells exhibited similar tumorigenicity <it>in vitro </it>and <it>in vivo</it>. Additionally, for the hTERT cells, SP rather than CD133 expression showed an 8-fold enhanced tumorigenic potential. The data suggest that SP cells, rather than those with CD133 marker, contain the rare population of CSC capable of producing prostate tumors.</p> <p>Conclusion</p> <p>Collectively, our data suggest that although CD133 is expressed only in a small population of hTERT-immortalized prostate cancer cells, it is not likely to be associated with stem cells, as CD133- and CD133+ cells exhibited similar tumorigenicity. However, SP isolated cells, appear to be enriched with tumorigenic stem-like cells capable of generating palpable tumors.</p>http://www.molecular-cancer.com/content/10/1/112Cancer Stem CellsCD133Side population (SP)prostate cancer
spellingShingle Wolcott Karen
Cannon Virginetta
Wang Honghe
Zhou Jianjun
Song Hongbin
Yates Clayton
Side population rather than CD133<sup>+ </sup>cells distinguishes enriched tumorigenicity in hTERT-immortalized primary prostate cancer cells
Molecular Cancer
Cancer Stem Cells
CD133
Side population (SP)
prostate cancer
title Side population rather than CD133<sup>+ </sup>cells distinguishes enriched tumorigenicity in hTERT-immortalized primary prostate cancer cells
title_full Side population rather than CD133<sup>+ </sup>cells distinguishes enriched tumorigenicity in hTERT-immortalized primary prostate cancer cells
title_fullStr Side population rather than CD133<sup>+ </sup>cells distinguishes enriched tumorigenicity in hTERT-immortalized primary prostate cancer cells
title_full_unstemmed Side population rather than CD133<sup>+ </sup>cells distinguishes enriched tumorigenicity in hTERT-immortalized primary prostate cancer cells
title_short Side population rather than CD133<sup>+ </sup>cells distinguishes enriched tumorigenicity in hTERT-immortalized primary prostate cancer cells
title_sort side population rather than cd133 sup sup cells distinguishes enriched tumorigenicity in htert immortalized primary prostate cancer cells
topic Cancer Stem Cells
CD133
Side population (SP)
prostate cancer
url http://www.molecular-cancer.com/content/10/1/112
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