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Somatic deletion of KDM1A/LSD1 gene is associated to advanced colorectal cancer stages
AIMS: KDM1A/LSD1 and ZNF217 are involved in a protein complex that participates in transcriptional regulation. ZNF217 has been analysed in numerous cancers and its amplification has been associated with advanced stages of disease; however, a similar role for KDM1A/LSD1 has not been uncovered. In thi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027028/ https://www.ncbi.nlm.nih.gov/pubmed/31471467 http://dx.doi.org/10.1136/jclinpath-2019-206128 |
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author | Ramírez-Ramírez, Ruth Gutiérrez-Angulo, Melva Peregrina-Sandoval, Jorge Moreno-Ortiz, José Miguel Franco-Topete, Ramon Antonio Cerda-Camacho, Felipe de Jesús Ayala-Madrigal, Maria de la Luz |
author_facet | Ramírez-Ramírez, Ruth Gutiérrez-Angulo, Melva Peregrina-Sandoval, Jorge Moreno-Ortiz, José Miguel Franco-Topete, Ramon Antonio Cerda-Camacho, Felipe de Jesús Ayala-Madrigal, Maria de la Luz |
author_sort | Ramírez-Ramírez, Ruth |
collection | PubMed |
description | AIMS: KDM1A/LSD1 and ZNF217 are involved in a protein complex that participates in transcriptional regulation. ZNF217 has been analysed in numerous cancers and its amplification has been associated with advanced stages of disease; however, a similar role for KDM1A/LSD1 has not been uncovered. In this study, we estimated the number of KDM1A/LSD1 and ZNF217 gene copies in tissue samples from patients diagnosed with colorectal cancer (CRC), as well as its association with clinicopathological features in patients with CRC. METHODS: Paraffin-embedded tumour samples from 50 patients with CRC with a histopathological diagnosis of CRC were included. The number of copies of KDM1A/LSD1 and ZNF217 genes was determined by fluorescence in situ hybridisation (FISH). We also analysed the association between copy numbers of selected genes and clinicopathological data based on multivariate analysis. RESULTS: Deletion of the KDM1A/LSD1 gene occurred in 19 samples (38%), whereas ZNF217 gene amplification was identified in 11 samples (22%). We found a significant association between lymph node metastasis or advanced tumour stage and KDM1A/LSD1 gene deletion (p value=0.0003 and p value=0.011, respectively). CONCLUSIONS: KDM1A/LSD1 gene deletion could be considered a novel prognostic biomarker of late-stage CRC. |
format | Online Article Text |
id | pubmed-7027028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-70270282020-02-28 Somatic deletion of KDM1A/LSD1 gene is associated to advanced colorectal cancer stages Ramírez-Ramírez, Ruth Gutiérrez-Angulo, Melva Peregrina-Sandoval, Jorge Moreno-Ortiz, José Miguel Franco-Topete, Ramon Antonio Cerda-Camacho, Felipe de Jesús Ayala-Madrigal, Maria de la Luz J Clin Pathol Original Research AIMS: KDM1A/LSD1 and ZNF217 are involved in a protein complex that participates in transcriptional regulation. ZNF217 has been analysed in numerous cancers and its amplification has been associated with advanced stages of disease; however, a similar role for KDM1A/LSD1 has not been uncovered. In this study, we estimated the number of KDM1A/LSD1 and ZNF217 gene copies in tissue samples from patients diagnosed with colorectal cancer (CRC), as well as its association with clinicopathological features in patients with CRC. METHODS: Paraffin-embedded tumour samples from 50 patients with CRC with a histopathological diagnosis of CRC were included. The number of copies of KDM1A/LSD1 and ZNF217 genes was determined by fluorescence in situ hybridisation (FISH). We also analysed the association between copy numbers of selected genes and clinicopathological data based on multivariate analysis. RESULTS: Deletion of the KDM1A/LSD1 gene occurred in 19 samples (38%), whereas ZNF217 gene amplification was identified in 11 samples (22%). We found a significant association between lymph node metastasis or advanced tumour stage and KDM1A/LSD1 gene deletion (p value=0.0003 and p value=0.011, respectively). CONCLUSIONS: KDM1A/LSD1 gene deletion could be considered a novel prognostic biomarker of late-stage CRC. BMJ Publishing Group 2020-02 2019-08-30 /pmc/articles/PMC7027028/ /pubmed/31471467 http://dx.doi.org/10.1136/jclinpath-2019-206128 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Original Research Ramírez-Ramírez, Ruth Gutiérrez-Angulo, Melva Peregrina-Sandoval, Jorge Moreno-Ortiz, José Miguel Franco-Topete, Ramon Antonio Cerda-Camacho, Felipe de Jesús Ayala-Madrigal, Maria de la Luz Somatic deletion of KDM1A/LSD1 gene is associated to advanced colorectal cancer stages |
title | Somatic deletion of KDM1A/LSD1 gene is associated to advanced colorectal cancer stages |
title_full | Somatic deletion of KDM1A/LSD1 gene is associated to advanced colorectal cancer stages |
title_fullStr | Somatic deletion of KDM1A/LSD1 gene is associated to advanced colorectal cancer stages |
title_full_unstemmed | Somatic deletion of KDM1A/LSD1 gene is associated to advanced colorectal cancer stages |
title_short | Somatic deletion of KDM1A/LSD1 gene is associated to advanced colorectal cancer stages |
title_sort | somatic deletion of kdm1a/lsd1 gene is associated to advanced colorectal cancer stages |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027028/ https://www.ncbi.nlm.nih.gov/pubmed/31471467 http://dx.doi.org/10.1136/jclinpath-2019-206128 |
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