Identification of CEA-interacting proteins in colon cancer cells and their changes in expression after irradiation.
- Author:
Byong Chul YOO
1
;
Seung Gu YEO
Author Information
- Publication Type:Original Article
- Keywords: Carcinoembryonic antigen; Colorectal neoplasms; Rab-6B; Lysozyme C; Radiation
- MeSH: Blotting, Western; Carcinoembryonic Antigen; Cell Line; Colon*; Colonic Neoplasms*; Colorectal Neoplasms; Immunoglobulin G; Immunoprecipitation; Mass Spectrometry; Membranes; Muramidase; Radiotherapy; Rectal Neoplasms
- From:Radiation Oncology Journal 2017;35(3):281-288
- CountryRepublic of Korea
- Language:English
- Abstract: 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.
