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...

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Main Authors: Maciej Tarnowski, Michał Czerewaty, Anna Deskur, Krzysztof Safranow, Wojciech Marlicz, Elżbieta Urasińska, Mariusz Z. Ratajczak, Teresa Starzyńska
Format: Article
Language:English
Published: Hindawi Limited 2016-01-01
Series:Disease Markers
Online Access:http://dx.doi.org/10.1155/2016/1987505
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spelling doaj-55b54937e8cb41478ddab03db13211be2020-11-24T22:25:19ZengHindawi LimitedDisease Markers0278-02401875-86302016-01-01201610.1155/2016/19875051987505Expression of Cancer Testis Antigens in Colorectal Cancer: New Prognostic and Therapeutic ImplicationsMaciej Tarnowski0Michał Czerewaty1Anna Deskur2Krzysztof Safranow3Wojciech Marlicz4Elżbieta Urasińska5Mariusz Z. Ratajczak6Teresa Starzyńska7Department of Physiology, Pomeranian Medical University, 70-111 Szczecin, PolandDepartment of Physiology, Pomeranian Medical University, 70-111 Szczecin, PolandDepartment of Gastroenterology, Pomeranian Medical University, 70-111 Szczecin, PolandDepartment of Biochemistry and Medical Chemistry, Pomeranian Medical University, 70-111 Szczecin, PolandDepartment of Gastroenterology, Pomeranian Medical University, 70-111 Szczecin, PolandDepartment of Pathomorphology, Pomeranian Medical University, 70-111 Szczecin, PolandDepartment of Physiology, Pomeranian Medical University, 70-111 Szczecin, PolandDepartment of Gastroenterology, Pomeranian Medical University, 70-111 Szczecin, PolandBackground. 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.http://dx.doi.org/10.1155/2016/1987505
collection DOAJ
language English
format Article
sources DOAJ
author Maciej Tarnowski
Michał Czerewaty
Anna Deskur
Krzysztof Safranow
Wojciech Marlicz
Elżbieta Urasińska
Mariusz Z. Ratajczak
Teresa Starzyńska
spellingShingle Maciej Tarnowski
Michał Czerewaty
Anna Deskur
Krzysztof Safranow
Wojciech Marlicz
Elżbieta Urasińska
Mariusz Z. Ratajczak
Teresa Starzyńska
Expression of Cancer Testis Antigens in Colorectal Cancer: New Prognostic and Therapeutic Implications
Disease Markers
author_facet Maciej Tarnowski
Michał Czerewaty
Anna Deskur
Krzysztof Safranow
Wojciech Marlicz
Elżbieta Urasińska
Mariusz Z. Ratajczak
Teresa Starzyńska
author_sort Maciej Tarnowski
title 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_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_sort expression of cancer testis antigens in colorectal cancer: new prognostic and therapeutic implications
publisher Hindawi Limited
series Disease Markers
issn 0278-0240
1875-8630
publishDate 2016-01-01
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.
url http://dx.doi.org/10.1155/2016/1987505
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