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Drug-resistant colon cancer cells produce high carcinoembryonic antigen and might not be cancer-initiating cells

PURPOSE: We evaluated the higher levels of carcinoembryonic antigen (CEA) secreted by the LoVo human colon carcinoma cells in a medium containing anticancer drugs. Drug-resistant LoVo cells were analyzed by subcutaneously xenotransplanting them into mice. The aim of this study was to evaluate whethe...

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Autores principales: Lee, Hsin-chung, Ling, Qing-Dong, Yu, Wan-Chun, Hung, Chunh-Ming, Kao, Ta-Chun, Huang, Yi-Wei, Higuchi, Akon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3693723/
https://www.ncbi.nlm.nih.gov/pubmed/23818760
http://dx.doi.org/10.2147/DDDT.S45890
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author Lee, Hsin-chung
Ling, Qing-Dong
Yu, Wan-Chun
Hung, Chunh-Ming
Kao, Ta-Chun
Huang, Yi-Wei
Higuchi, Akon
author_facet Lee, Hsin-chung
Ling, Qing-Dong
Yu, Wan-Chun
Hung, Chunh-Ming
Kao, Ta-Chun
Huang, Yi-Wei
Higuchi, Akon
author_sort Lee, Hsin-chung
collection PubMed
description PURPOSE: We evaluated the higher levels of carcinoembryonic antigen (CEA) secreted by the LoVo human colon carcinoma cells in a medium containing anticancer drugs. Drug-resistant LoVo cells were analyzed by subcutaneously xenotransplanting them into mice. The aim of this study was to evaluate whether the drug-resistant cells isolated in this study were cancer-initiating cells, known also as cancer stem cells (CSCs). METHODS: The production of CEA was investigated in LoVo cells that were cultured with 0–10 mM of anticancer drugs, and we evaluated the increase in CEA production by the LoVo cells that were stimulated by anticancer drug treatment. The expression of several CSC markers in LoVo cells treated with anticancer drugs was also evaluated. Following anticancer drug treatment, LoVo cells were injected subcutaneously into the flanks of severe combined immunodeficiency mice in order to evaluate the CSC fraction. RESULTS: Production of CEA by LoVo cells was stimulated by the addition of anticancer drugs. Drug-resistant LoVo cells expressed lower levels of CSC markers, and LoVo cells treated with any of the anticancer drugs tested did not generate tumors within 8 weeks from when the cells were injected subcutaneously into severe combined immunodeficiency mice. These results suggest that the drug-resistant LoVo cells have a smaller population of CSCs than the untreated LoVo cells. CONCLUSION: Production of CEA by LoVo cells can be stimulated by the addition of anticancer drugs. The drug-resistant subpopulation of LoVo colon cancer cells could stimulate the production of CEA, but these cells did not act as CSCs in in vivo tumor generation experiments.
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spelling pubmed-36937232013-07-01 Drug-resistant colon cancer cells produce high carcinoembryonic antigen and might not be cancer-initiating cells Lee, Hsin-chung Ling, Qing-Dong Yu, Wan-Chun Hung, Chunh-Ming Kao, Ta-Chun Huang, Yi-Wei Higuchi, Akon Drug Des Devel Ther Original Research PURPOSE: We evaluated the higher levels of carcinoembryonic antigen (CEA) secreted by the LoVo human colon carcinoma cells in a medium containing anticancer drugs. Drug-resistant LoVo cells were analyzed by subcutaneously xenotransplanting them into mice. The aim of this study was to evaluate whether the drug-resistant cells isolated in this study were cancer-initiating cells, known also as cancer stem cells (CSCs). METHODS: The production of CEA was investigated in LoVo cells that were cultured with 0–10 mM of anticancer drugs, and we evaluated the increase in CEA production by the LoVo cells that were stimulated by anticancer drug treatment. The expression of several CSC markers in LoVo cells treated with anticancer drugs was also evaluated. Following anticancer drug treatment, LoVo cells were injected subcutaneously into the flanks of severe combined immunodeficiency mice in order to evaluate the CSC fraction. RESULTS: Production of CEA by LoVo cells was stimulated by the addition of anticancer drugs. Drug-resistant LoVo cells expressed lower levels of CSC markers, and LoVo cells treated with any of the anticancer drugs tested did not generate tumors within 8 weeks from when the cells were injected subcutaneously into severe combined immunodeficiency mice. These results suggest that the drug-resistant LoVo cells have a smaller population of CSCs than the untreated LoVo cells. CONCLUSION: Production of CEA by LoVo cells can be stimulated by the addition of anticancer drugs. The drug-resistant subpopulation of LoVo colon cancer cells could stimulate the production of CEA, but these cells did not act as CSCs in in vivo tumor generation experiments. Dove Medical Press 2013-06-17 /pmc/articles/PMC3693723/ /pubmed/23818760 http://dx.doi.org/10.2147/DDDT.S45890 Text en © 2013 Lee et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Lee, Hsin-chung
Ling, Qing-Dong
Yu, Wan-Chun
Hung, Chunh-Ming
Kao, Ta-Chun
Huang, Yi-Wei
Higuchi, Akon
Drug-resistant colon cancer cells produce high carcinoembryonic antigen and might not be cancer-initiating cells
title Drug-resistant colon cancer cells produce high carcinoembryonic antigen and might not be cancer-initiating cells
title_full Drug-resistant colon cancer cells produce high carcinoembryonic antigen and might not be cancer-initiating cells
title_fullStr Drug-resistant colon cancer cells produce high carcinoembryonic antigen and might not be cancer-initiating cells
title_full_unstemmed Drug-resistant colon cancer cells produce high carcinoembryonic antigen and might not be cancer-initiating cells
title_short Drug-resistant colon cancer cells produce high carcinoembryonic antigen and might not be cancer-initiating cells
title_sort drug-resistant colon cancer cells produce high carcinoembryonic antigen and might not be cancer-initiating cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3693723/
https://www.ncbi.nlm.nih.gov/pubmed/23818760
http://dx.doi.org/10.2147/DDDT.S45890
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