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Prognostic relevance of a T-type calcium channels gene signature in solid tumours: A correlation ready for clinical validation
BACKGROUND: T-type calcium channels (TTCCs) mediate calcium influx across the cell membrane. TTCCs regulate numerous physiological processes including cardiac pacemaking and neuronal activity. In addition, they have been implicated in the proliferation, migration and differentiation of tumour tissue...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573204/ https://www.ncbi.nlm.nih.gov/pubmed/28846697 http://dx.doi.org/10.1371/journal.pone.0182818 |
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author | Fornaro, Lorenzo Vivaldi, Caterina Lin, Dong Xue, Hui Falcone, Alfredo Wang, Yuzhuo Crea, Francesco Bootman, Martin D. |
author_facet | Fornaro, Lorenzo Vivaldi, Caterina Lin, Dong Xue, Hui Falcone, Alfredo Wang, Yuzhuo Crea, Francesco Bootman, Martin D. |
author_sort | Fornaro, Lorenzo |
collection | PubMed |
description | BACKGROUND: T-type calcium channels (TTCCs) mediate calcium influx across the cell membrane. TTCCs regulate numerous physiological processes including cardiac pacemaking and neuronal activity. In addition, they have been implicated in the proliferation, migration and differentiation of tumour tissues. Although the signalling events downstream of TTCC-mediated calcium influx are not fully elucidated, it is clear that variations in the expression of TTCCs promote tumour formation and hinder response to treatment. METHODS: We examined the expression of TTCC genes (all three subtypes; CACNA-1G, CACNA-1H and CACNA-1I) and their prognostic value in three major solid tumours (i.e. gastric, lung and ovarian cancers) via a publicly accessible database. RESULTS: In gastric cancer, expression of all the CACNA genes was associated with overall survival (OS) among stage I-IV patients (all p<0.05). By combining the three potential biomarkers, a TTCC signature was developed, which retained a significant association with OS both in stage IV and stage I-III patients. In lung and ovarian cancer, association with OS was also significant when all tumour stages were considered, but was partly lost or inconclusive after splitting cases into localized and metastatic subsets. CONCLUSIONS: Alterations in CACNA gene expression are linked to tumour prognosis. Gastric cancer represents the most promising setting for further evaluation. |
format | Online Article Text |
id | pubmed-5573204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55732042017-09-09 Prognostic relevance of a T-type calcium channels gene signature in solid tumours: A correlation ready for clinical validation Fornaro, Lorenzo Vivaldi, Caterina Lin, Dong Xue, Hui Falcone, Alfredo Wang, Yuzhuo Crea, Francesco Bootman, Martin D. PLoS One Research Article BACKGROUND: T-type calcium channels (TTCCs) mediate calcium influx across the cell membrane. TTCCs regulate numerous physiological processes including cardiac pacemaking and neuronal activity. In addition, they have been implicated in the proliferation, migration and differentiation of tumour tissues. Although the signalling events downstream of TTCC-mediated calcium influx are not fully elucidated, it is clear that variations in the expression of TTCCs promote tumour formation and hinder response to treatment. METHODS: We examined the expression of TTCC genes (all three subtypes; CACNA-1G, CACNA-1H and CACNA-1I) and their prognostic value in three major solid tumours (i.e. gastric, lung and ovarian cancers) via a publicly accessible database. RESULTS: In gastric cancer, expression of all the CACNA genes was associated with overall survival (OS) among stage I-IV patients (all p<0.05). By combining the three potential biomarkers, a TTCC signature was developed, which retained a significant association with OS both in stage IV and stage I-III patients. In lung and ovarian cancer, association with OS was also significant when all tumour stages were considered, but was partly lost or inconclusive after splitting cases into localized and metastatic subsets. CONCLUSIONS: Alterations in CACNA gene expression are linked to tumour prognosis. Gastric cancer represents the most promising setting for further evaluation. Public Library of Science 2017-08-28 /pmc/articles/PMC5573204/ /pubmed/28846697 http://dx.doi.org/10.1371/journal.pone.0182818 Text en © 2017 Fornaro et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Fornaro, Lorenzo Vivaldi, Caterina Lin, Dong Xue, Hui Falcone, Alfredo Wang, Yuzhuo Crea, Francesco Bootman, Martin D. Prognostic relevance of a T-type calcium channels gene signature in solid tumours: A correlation ready for clinical validation |
title | Prognostic relevance of a T-type calcium channels gene signature in solid tumours: A correlation ready for clinical validation |
title_full | Prognostic relevance of a T-type calcium channels gene signature in solid tumours: A correlation ready for clinical validation |
title_fullStr | Prognostic relevance of a T-type calcium channels gene signature in solid tumours: A correlation ready for clinical validation |
title_full_unstemmed | Prognostic relevance of a T-type calcium channels gene signature in solid tumours: A correlation ready for clinical validation |
title_short | Prognostic relevance of a T-type calcium channels gene signature in solid tumours: A correlation ready for clinical validation |
title_sort | prognostic relevance of a t-type calcium channels gene signature in solid tumours: a correlation ready for clinical validation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5573204/ https://www.ncbi.nlm.nih.gov/pubmed/28846697 http://dx.doi.org/10.1371/journal.pone.0182818 |
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