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Identification of CEA-interacting proteins in colon cancer cells and their changes in expression after irradiation

PURPOSE: The serum carcinoembryonic antigen (CEA) level has been recognized as a prognostic factor in colorectal cancer, and associated with response of rectal cancer to radiotherapy. This study aimed to identify CEA-interacting proteins in colon cancer cells and observe post-irradiation changes in...

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Autores principales: Yoo, Byong Chul, Yeo, Seung-Gu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Radiation Oncology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654139/
https://www.ncbi.nlm.nih.gov/pubmed/28881503
http://dx.doi.org/10.3857/roj.2017.00255
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author Yoo, Byong Chul
Yeo, Seung-Gu
author_facet Yoo, Byong Chul
Yeo, Seung-Gu
author_sort Yoo, Byong Chul
collection PubMed
description PURPOSE: The serum carcinoembryonic antigen (CEA) level has been recognized as a prognostic factor in colorectal cancer, and associated with response of rectal cancer to radiotherapy. This study aimed to identify CEA-interacting proteins in colon cancer cells and observe post-irradiation changes in their expression. MATERIALS AND METHODS: CEA expression in colon cancer cells was examined by Western blot analysis. Using an anti-CEA antibody or IgG as a negative control, immunoprecipitation was performed in colon cancer cell lysates. CEA and IgG immunoprecipitates were used for liquid chromatography–tandem mass spectrometry (LC-MS/MS) analysis. Proteins identified in the CEA immunoprecipitates but not in the IgG immunoprecipitates were selected as CEA-interacting proteins. After radiation treatment, changes in expression of CEA-interacting proteins were monitored by Western blot analysis. RESULTS: CEA expression was higher in SNU-81 cells compared with LoVo cells. The membrane localization of CEA limited the immunoprecipitation results and thus the number of CEA-interacting proteins identified. Only the Ras-related protein Rab-6B and lysozyme C were identified as CEA-interacting proteins in LoVo and SNU-81 cells, respectively. Lysozyme C was detected only in SNU-81, and CEA expression was differently regulated in two cell lines; it was down-regulated in LoVo but up-regulated in SNU-81 in radiation dosage-dependent manner. CONCLUSION: CEA-mediated radiation response appears to vary, depending on the characteristics of individual cancer cells. The lysozyme C and Rab subfamily proteins may play a role in the link between CEA and tumor response to radiation, although further studies are needed to clarify functional roles of the identified proteins.
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spelling pubmed-56541392017-10-24 Identification of CEA-interacting proteins in colon cancer cells and their changes in expression after irradiation Yoo, Byong Chul Yeo, Seung-Gu Radiat Oncol J Original Article PURPOSE: The serum carcinoembryonic antigen (CEA) level has been recognized as a prognostic factor in colorectal cancer, and associated with response of rectal cancer to radiotherapy. This study aimed to identify CEA-interacting proteins in colon cancer cells and observe post-irradiation changes in their expression. MATERIALS AND METHODS: CEA expression in colon cancer cells was examined by Western blot analysis. Using an anti-CEA antibody or IgG as a negative control, immunoprecipitation was performed in colon cancer cell lysates. CEA and IgG immunoprecipitates were used for liquid chromatography–tandem mass spectrometry (LC-MS/MS) analysis. Proteins identified in the CEA immunoprecipitates but not in the IgG immunoprecipitates were selected as CEA-interacting proteins. After radiation treatment, changes in expression of CEA-interacting proteins were monitored by Western blot analysis. RESULTS: CEA expression was higher in SNU-81 cells compared with LoVo cells. The membrane localization of CEA limited the immunoprecipitation results and thus the number of CEA-interacting proteins identified. Only the Ras-related protein Rab-6B and lysozyme C were identified as CEA-interacting proteins in LoVo and SNU-81 cells, respectively. Lysozyme C was detected only in SNU-81, and CEA expression was differently regulated in two cell lines; it was down-regulated in LoVo but up-regulated in SNU-81 in radiation dosage-dependent manner. CONCLUSION: CEA-mediated radiation response appears to vary, depending on the characteristics of individual cancer cells. The lysozyme C and Rab subfamily proteins may play a role in the link between CEA and tumor response to radiation, although further studies are needed to clarify functional roles of the identified proteins. The Korean Society for Radiation Oncology 2017-09 2017-09-15 /pmc/articles/PMC5654139/ /pubmed/28881503 http://dx.doi.org/10.3857/roj.2017.00255 Text en Copyright © 2017 The Korean Society for Radiation Oncology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (http://creativecommons.org/licenses/by-nc/4.0) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yoo, Byong Chul
Yeo, Seung-Gu
Identification of CEA-interacting proteins in colon cancer cells and their changes in expression after irradiation
title Identification of CEA-interacting proteins in colon cancer cells and their changes in expression after irradiation
title_full Identification of CEA-interacting proteins in colon cancer cells and their changes in expression after irradiation
title_fullStr Identification of CEA-interacting proteins in colon cancer cells and their changes in expression after irradiation
title_full_unstemmed Identification of CEA-interacting proteins in colon cancer cells and their changes in expression after irradiation
title_short Identification of CEA-interacting proteins in colon cancer cells and their changes in expression after irradiation
title_sort identification of cea-interacting proteins in colon cancer cells and their changes in expression after irradiation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654139/
https://www.ncbi.nlm.nih.gov/pubmed/28881503
http://dx.doi.org/10.3857/roj.2017.00255
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