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Isolation and enrichment of PC-3 prostate cancer stem-like cells using MACS and serum-free medium

Prostate cancer stem-like cells (PCSLCs) are considered to be the ‘seed’ of prostate cancer. The aim of this study was to confirm that the PC-3 cells, which we isolated and enriched from PC-3 cells through magnetic bead cell sorting (MACS) and serum-free medium (SFM) culture, were PCSLCs. Combinatio...

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Autores principales: SHENG, XIA, LI, ZENG, WANG, DE-LIN, LI, WEN-BIN, LUO, ZHAO, CHEN, KE-HONG, CAO, JIAN-JIA, YU, CHAO, LIU, WU-JIANG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3576206/
https://www.ncbi.nlm.nih.gov/pubmed/23426586
http://dx.doi.org/10.3892/ol.2012.1090
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author SHENG, XIA
LI, ZENG
WANG, DE-LIN
LI, WEN-BIN
LUO, ZHAO
CHEN, KE-HONG
CAO, JIAN-JIA
YU, CHAO
LIU, WU-JIANG
author_facet SHENG, XIA
LI, ZENG
WANG, DE-LIN
LI, WEN-BIN
LUO, ZHAO
CHEN, KE-HONG
CAO, JIAN-JIA
YU, CHAO
LIU, WU-JIANG
author_sort SHENG, XIA
collection PubMed
description Prostate cancer stem-like cells (PCSLCs) are considered to be the ‘seed’ of prostate cancer. The aim of this study was to confirm that the PC-3 cells, which we isolated and enriched from PC-3 cells through magnetic bead cell sorting (MACS) and serum-free medium (SFM) culture, were PCSLCs. Combinations of MACS, flow cytometry (FCM), SFM and immunocytochemistry (ICC) were used to ensure the positive expression of CD133 and CD44 on PC-3 and sphere-forming cell membranes. Self-renewal, multi-potential differentiation, unlimited proliferation and permanency assays were also applied to indentify whether the PC-3 cells exhibited the characteristics of cancer stem cells (CSCs). As a result, there was a low proportion of PCSLCs in the PC-3 cells. In the FCM assay, the proportion of cells expressing CD133 or CD44 in the PC-3 cells was 0.51 and 0.31%, respectively. In addition, we found that the proportion of PC-3 cells sorted by MACS that expressed CD133 was significantly increased compared with that of the sphere-forming cells cultured in SFM (99.09 vs. 84.80%, P<0.05), while no difference was observed in the proportion of cells expressing CD44 between them (99.88 vs. 99.82%, P>0.05). The expression of PAP and AR as detected by western blot analysis of induced PCSLCs was significantly increased compared with that of uninduced PCSLCs (P<0.05); the proliferation capacity of PCSLCs was significantly higher than that of both the PC-3 cells (P<0.05) and induced PCSLCs (P<0.05). Furthermore, the PCSLCs that were isolated from SFM and MACS both demonstrated certain characteristics of stem cells and should be considered as stem cell-like. These data may hold potential for further exploring the role of PCSLCs.
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spelling pubmed-35762062013-02-20 Isolation and enrichment of PC-3 prostate cancer stem-like cells using MACS and serum-free medium SHENG, XIA LI, ZENG WANG, DE-LIN LI, WEN-BIN LUO, ZHAO CHEN, KE-HONG CAO, JIAN-JIA YU, CHAO LIU, WU-JIANG Oncol Lett Articles Prostate cancer stem-like cells (PCSLCs) are considered to be the ‘seed’ of prostate cancer. The aim of this study was to confirm that the PC-3 cells, which we isolated and enriched from PC-3 cells through magnetic bead cell sorting (MACS) and serum-free medium (SFM) culture, were PCSLCs. Combinations of MACS, flow cytometry (FCM), SFM and immunocytochemistry (ICC) were used to ensure the positive expression of CD133 and CD44 on PC-3 and sphere-forming cell membranes. Self-renewal, multi-potential differentiation, unlimited proliferation and permanency assays were also applied to indentify whether the PC-3 cells exhibited the characteristics of cancer stem cells (CSCs). As a result, there was a low proportion of PCSLCs in the PC-3 cells. In the FCM assay, the proportion of cells expressing CD133 or CD44 in the PC-3 cells was 0.51 and 0.31%, respectively. In addition, we found that the proportion of PC-3 cells sorted by MACS that expressed CD133 was significantly increased compared with that of the sphere-forming cells cultured in SFM (99.09 vs. 84.80%, P<0.05), while no difference was observed in the proportion of cells expressing CD44 between them (99.88 vs. 99.82%, P>0.05). The expression of PAP and AR as detected by western blot analysis of induced PCSLCs was significantly increased compared with that of uninduced PCSLCs (P<0.05); the proliferation capacity of PCSLCs was significantly higher than that of both the PC-3 cells (P<0.05) and induced PCSLCs (P<0.05). Furthermore, the PCSLCs that were isolated from SFM and MACS both demonstrated certain characteristics of stem cells and should be considered as stem cell-like. These data may hold potential for further exploring the role of PCSLCs. D.A. Spandidos 2013-03 2012-12-21 /pmc/articles/PMC3576206/ /pubmed/23426586 http://dx.doi.org/10.3892/ol.2012.1090 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
SHENG, XIA
LI, ZENG
WANG, DE-LIN
LI, WEN-BIN
LUO, ZHAO
CHEN, KE-HONG
CAO, JIAN-JIA
YU, CHAO
LIU, WU-JIANG
Isolation and enrichment of PC-3 prostate cancer stem-like cells using MACS and serum-free medium
title Isolation and enrichment of PC-3 prostate cancer stem-like cells using MACS and serum-free medium
title_full Isolation and enrichment of PC-3 prostate cancer stem-like cells using MACS and serum-free medium
title_fullStr Isolation and enrichment of PC-3 prostate cancer stem-like cells using MACS and serum-free medium
title_full_unstemmed Isolation and enrichment of PC-3 prostate cancer stem-like cells using MACS and serum-free medium
title_short Isolation and enrichment of PC-3 prostate cancer stem-like cells using MACS and serum-free medium
title_sort isolation and enrichment of pc-3 prostate cancer stem-like cells using macs and serum-free medium
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3576206/
https://www.ncbi.nlm.nih.gov/pubmed/23426586
http://dx.doi.org/10.3892/ol.2012.1090
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