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Expression of Cancer Testis Antigens in Colorectal Cancer: New Prognostic and Therapeutic Implications
Background. While cancer/testis antigens (CTAs) are restricted in postnatal tissues to testes and germ line-derived cells, their role in cancer development and the clinical significance of their expression still remain to be better defined. Objective. The aim of this study was to investigate the lev...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007337/ https://www.ncbi.nlm.nih.gov/pubmed/27635108 http://dx.doi.org/10.1155/2016/1987505 |
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author | Tarnowski, Maciej Czerewaty, Michał Deskur, Anna Safranow, Krzysztof Marlicz, Wojciech Urasińska, Elżbieta Ratajczak, Mariusz Z. Starzyńska, Teresa |
author_facet | Tarnowski, Maciej Czerewaty, Michał Deskur, Anna Safranow, Krzysztof Marlicz, Wojciech Urasińska, Elżbieta Ratajczak, Mariusz Z. Starzyńska, Teresa |
author_sort | Tarnowski, Maciej |
collection | PubMed |
description | Background. While cancer/testis antigens (CTAs) are restricted in postnatal tissues to testes and germ line-derived cells, their role in cancer development and the clinical significance of their expression still remain to be better defined. Objective. The aim of this study was to investigate the level of CTA expression in colon samples from patients with colorectal cancer (CRC) in relation to patient clinical status. Methods. Forty-five patients with newly diagnosed colorectal cancer were included in the study. We selected a panel of 18 CTAs that were previously detected in CRC as well as some new gene candidates, and their expression was detected at the mRNA level by employing RQ-PCR. Additionally, we evaluated CTA expression in three colon cancer cell lines (CL-188, HTB-39, and HTB-37) after exposure to the DNA methylation-modifying drug 5-azacytidine. Results. We report that 6 out of 18 (33%) CTAs tested (MAGEA3, OIP5, TTK, PLU1, DKKL1, and FBXO39) were significantly (p < 0.05) overexpressed in tumor tissue compared with healthy colon samples isolated from the same patients. Conclusions. Moreover, we found that MAGEA3, PLU-1, and DKKL expression positively correlated with disease progression, evaluated according to the Dukes staging system. Finally, 5-azacytidine exposure significantly upregulated expression of CTAs on CRC cells, which indicates that this demethylation agent could be employed therapeutically to enhance the immune response against tumor cells. |
format | Online Article Text |
id | pubmed-5007337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-50073372016-09-15 Expression of Cancer Testis Antigens in Colorectal Cancer: New Prognostic and Therapeutic Implications Tarnowski, Maciej Czerewaty, Michał Deskur, Anna Safranow, Krzysztof Marlicz, Wojciech Urasińska, Elżbieta Ratajczak, Mariusz Z. Starzyńska, Teresa Dis Markers Research Article Background. While cancer/testis antigens (CTAs) are restricted in postnatal tissues to testes and germ line-derived cells, their role in cancer development and the clinical significance of their expression still remain to be better defined. Objective. The aim of this study was to investigate the level of CTA expression in colon samples from patients with colorectal cancer (CRC) in relation to patient clinical status. Methods. Forty-five patients with newly diagnosed colorectal cancer were included in the study. We selected a panel of 18 CTAs that were previously detected in CRC as well as some new gene candidates, and their expression was detected at the mRNA level by employing RQ-PCR. Additionally, we evaluated CTA expression in three colon cancer cell lines (CL-188, HTB-39, and HTB-37) after exposure to the DNA methylation-modifying drug 5-azacytidine. Results. We report that 6 out of 18 (33%) CTAs tested (MAGEA3, OIP5, TTK, PLU1, DKKL1, and FBXO39) were significantly (p < 0.05) overexpressed in tumor tissue compared with healthy colon samples isolated from the same patients. Conclusions. Moreover, we found that MAGEA3, PLU-1, and DKKL expression positively correlated with disease progression, evaluated according to the Dukes staging system. Finally, 5-azacytidine exposure significantly upregulated expression of CTAs on CRC cells, which indicates that this demethylation agent could be employed therapeutically to enhance the immune response against tumor cells. Hindawi Publishing Corporation 2016 2016-08-18 /pmc/articles/PMC5007337/ /pubmed/27635108 http://dx.doi.org/10.1155/2016/1987505 Text en Copyright © 2016 Maciej Tarnowski et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Tarnowski, Maciej Czerewaty, Michał Deskur, Anna Safranow, Krzysztof Marlicz, Wojciech Urasińska, Elżbieta Ratajczak, Mariusz Z. Starzyńska, Teresa Expression of Cancer Testis Antigens in Colorectal Cancer: New Prognostic and Therapeutic Implications |
title | Expression of Cancer Testis Antigens in Colorectal Cancer: New Prognostic and Therapeutic Implications |
title_full | Expression of Cancer Testis Antigens in Colorectal Cancer: New Prognostic and Therapeutic Implications |
title_fullStr | Expression of Cancer Testis Antigens in Colorectal Cancer: New Prognostic and Therapeutic Implications |
title_full_unstemmed | Expression of Cancer Testis Antigens in Colorectal Cancer: New Prognostic and Therapeutic Implications |
title_short | Expression of Cancer Testis Antigens in Colorectal Cancer: New Prognostic and Therapeutic Implications |
title_sort | expression of cancer testis antigens in colorectal cancer: new prognostic and therapeutic implications |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007337/ https://www.ncbi.nlm.nih.gov/pubmed/27635108 http://dx.doi.org/10.1155/2016/1987505 |
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