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Prognostic Importance of Cell Cycle Regulators Cyclin D1 (CCND1) and Cyclin-Dependent Kinase Inhibitor 1B (CDKN1B/p27) in Sporadic Gastric Cancers

Background. Gastric cancer is known for a notable variety in the course of the disease. Clinical factors, such as tumor stage, grade, and localization, are key in patient survival. It is expected that molecular factors such as somatic mutations and gene amplifications are also underlying tumor biolo...

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Autores principales: Minarikova, Petra, Benesova, Lucie, Halkova, Tereza, Belsanova, Barbora, Tuckova, Inna, Belina, Frantisek, Dusek, Ladislav, Zavoral, Miroslav, Minarik, Marek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066010/
https://www.ncbi.nlm.nih.gov/pubmed/27781065
http://dx.doi.org/10.1155/2016/9408190
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author Minarikova, Petra
Benesova, Lucie
Halkova, Tereza
Belsanova, Barbora
Tuckova, Inna
Belina, Frantisek
Dusek, Ladislav
Zavoral, Miroslav
Minarik, Marek
author_facet Minarikova, Petra
Benesova, Lucie
Halkova, Tereza
Belsanova, Barbora
Tuckova, Inna
Belina, Frantisek
Dusek, Ladislav
Zavoral, Miroslav
Minarik, Marek
author_sort Minarikova, Petra
collection PubMed
description Background. Gastric cancer is known for a notable variety in the course of the disease. Clinical factors, such as tumor stage, grade, and localization, are key in patient survival. It is expected that molecular factors such as somatic mutations and gene amplifications are also underlying tumor biological behavior and may serve as factors for prognosis estimation. Aim. The purpose of this study was to examine gene amplifications from a panel of genes to uncover potential prognostic marker candidates. Methods. A panel of gene amplifications including 71 genes was tested by multiplex ligation-dependent probe amplification (MLPA) technique in 76 gastric cancer samples from a Caucasian population. The correlation of gene amplification status with patient survival was determined by the Kaplan-Meier method. Results. The amplification of two cell cycle regulators, CCND1 and CDKN1B, was identified to have a negative prognostic role. The medial survival of patients with gastric cancer displaying amplification compared to patients without amplification was 192 versus 725 days for CCND1 (P = 0.0012) and 165 versus 611 days for CDKN1B (P = 0.0098). Conclusion. Gene amplifications of CCND1 and CDKN1B are potential candidates to serve as prognostic markers for the stratification of patients based on the estimate of survival in the management of gastric cancer patients.
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spelling pubmed-50660102016-10-25 Prognostic Importance of Cell Cycle Regulators Cyclin D1 (CCND1) and Cyclin-Dependent Kinase Inhibitor 1B (CDKN1B/p27) in Sporadic Gastric Cancers Minarikova, Petra Benesova, Lucie Halkova, Tereza Belsanova, Barbora Tuckova, Inna Belina, Frantisek Dusek, Ladislav Zavoral, Miroslav Minarik, Marek Gastroenterol Res Pract Research Article Background. Gastric cancer is known for a notable variety in the course of the disease. Clinical factors, such as tumor stage, grade, and localization, are key in patient survival. It is expected that molecular factors such as somatic mutations and gene amplifications are also underlying tumor biological behavior and may serve as factors for prognosis estimation. Aim. The purpose of this study was to examine gene amplifications from a panel of genes to uncover potential prognostic marker candidates. Methods. A panel of gene amplifications including 71 genes was tested by multiplex ligation-dependent probe amplification (MLPA) technique in 76 gastric cancer samples from a Caucasian population. The correlation of gene amplification status with patient survival was determined by the Kaplan-Meier method. Results. The amplification of two cell cycle regulators, CCND1 and CDKN1B, was identified to have a negative prognostic role. The medial survival of patients with gastric cancer displaying amplification compared to patients without amplification was 192 versus 725 days for CCND1 (P = 0.0012) and 165 versus 611 days for CDKN1B (P = 0.0098). Conclusion. Gene amplifications of CCND1 and CDKN1B are potential candidates to serve as prognostic markers for the stratification of patients based on the estimate of survival in the management of gastric cancer patients. Hindawi Publishing Corporation 2016 2016-10-03 /pmc/articles/PMC5066010/ /pubmed/27781065 http://dx.doi.org/10.1155/2016/9408190 Text en Copyright © 2016 Petra Minarikova 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
Minarikova, Petra
Benesova, Lucie
Halkova, Tereza
Belsanova, Barbora
Tuckova, Inna
Belina, Frantisek
Dusek, Ladislav
Zavoral, Miroslav
Minarik, Marek
Prognostic Importance of Cell Cycle Regulators Cyclin D1 (CCND1) and Cyclin-Dependent Kinase Inhibitor 1B (CDKN1B/p27) in Sporadic Gastric Cancers
title Prognostic Importance of Cell Cycle Regulators Cyclin D1 (CCND1) and Cyclin-Dependent Kinase Inhibitor 1B (CDKN1B/p27) in Sporadic Gastric Cancers
title_full Prognostic Importance of Cell Cycle Regulators Cyclin D1 (CCND1) and Cyclin-Dependent Kinase Inhibitor 1B (CDKN1B/p27) in Sporadic Gastric Cancers
title_fullStr Prognostic Importance of Cell Cycle Regulators Cyclin D1 (CCND1) and Cyclin-Dependent Kinase Inhibitor 1B (CDKN1B/p27) in Sporadic Gastric Cancers
title_full_unstemmed Prognostic Importance of Cell Cycle Regulators Cyclin D1 (CCND1) and Cyclin-Dependent Kinase Inhibitor 1B (CDKN1B/p27) in Sporadic Gastric Cancers
title_short Prognostic Importance of Cell Cycle Regulators Cyclin D1 (CCND1) and Cyclin-Dependent Kinase Inhibitor 1B (CDKN1B/p27) in Sporadic Gastric Cancers
title_sort prognostic importance of cell cycle regulators cyclin d1 (ccnd1) and cyclin-dependent kinase inhibitor 1b (cdkn1b/p27) in sporadic gastric cancers
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5066010/
https://www.ncbi.nlm.nih.gov/pubmed/27781065
http://dx.doi.org/10.1155/2016/9408190
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