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TRPV2 Calcium Channel Gene Expression and Outcomes in Gastric Cancer Patients: A Clinically Relevant Association

Gastric cancer (GC) is characterized by poor efficacy and the modest clinical impact of current therapies. Apoptosis evasion represents a causative factor for treatment failure in GC as in other cancers. Since intracellular calcium homeostasis regulation has been found to be associated with apoptosi...

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Autores principales: Zoppoli, Pietro, Calice, Giovanni, Laurino, Simona, Ruggieri, Vitalba, La Rocca, Francesco, La Torre, Giuseppe, Ciuffi, Mario, Amendola, Elena, De Vita, Ferdinando, Petrillo, Angelica, Napolitano, Giuliana, Falco, Geppino, Russi, Sabino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572141/
https://www.ncbi.nlm.nih.gov/pubmed/31083561
http://dx.doi.org/10.3390/jcm8050662
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author Zoppoli, Pietro
Calice, Giovanni
Laurino, Simona
Ruggieri, Vitalba
La Rocca, Francesco
La Torre, Giuseppe
Ciuffi, Mario
Amendola, Elena
De Vita, Ferdinando
Petrillo, Angelica
Napolitano, Giuliana
Falco, Geppino
Russi, Sabino
author_facet Zoppoli, Pietro
Calice, Giovanni
Laurino, Simona
Ruggieri, Vitalba
La Rocca, Francesco
La Torre, Giuseppe
Ciuffi, Mario
Amendola, Elena
De Vita, Ferdinando
Petrillo, Angelica
Napolitano, Giuliana
Falco, Geppino
Russi, Sabino
author_sort Zoppoli, Pietro
collection PubMed
description Gastric cancer (GC) is characterized by poor efficacy and the modest clinical impact of current therapies. Apoptosis evasion represents a causative factor for treatment failure in GC as in other cancers. Since intracellular calcium homeostasis regulation has been found to be associated with apoptosis resistance, the aberrant expression of intracellular calcium regulator genes (CaRGs) could have a prognostic value in GC patients. We analyzed the association of the expression levels of 98 CaRGs with prognosis by the log-rank test in a collection of 1524 GC samples from four gene expression profiling datasets. We also evaluated differential gene expression in comparison with normal stomach tissue, and then we crossed results with tissue microarrays from the Human Protein Atlas. Among the investigated CaRGs, patients with high levels of TRPV2 expression were characterized by a shorter overall survival. TRPV2 expression was found to increase according to tumor stage. Both mRNA and protein levels were significantly higher in tumor than normal stomach samples. TRPV2 was also associated with poor prognosis in the Lauren’s intestinal type GC and in patients treated with adjuvant therapy. Overall, we highlighted the relevance of TRPV2 not only as a prognostic biomarker but also as a potential therapeutic target to improve GC treatment efficacy.
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spelling pubmed-65721412019-06-18 TRPV2 Calcium Channel Gene Expression and Outcomes in Gastric Cancer Patients: A Clinically Relevant Association Zoppoli, Pietro Calice, Giovanni Laurino, Simona Ruggieri, Vitalba La Rocca, Francesco La Torre, Giuseppe Ciuffi, Mario Amendola, Elena De Vita, Ferdinando Petrillo, Angelica Napolitano, Giuliana Falco, Geppino Russi, Sabino J Clin Med Article Gastric cancer (GC) is characterized by poor efficacy and the modest clinical impact of current therapies. Apoptosis evasion represents a causative factor for treatment failure in GC as in other cancers. Since intracellular calcium homeostasis regulation has been found to be associated with apoptosis resistance, the aberrant expression of intracellular calcium regulator genes (CaRGs) could have a prognostic value in GC patients. We analyzed the association of the expression levels of 98 CaRGs with prognosis by the log-rank test in a collection of 1524 GC samples from four gene expression profiling datasets. We also evaluated differential gene expression in comparison with normal stomach tissue, and then we crossed results with tissue microarrays from the Human Protein Atlas. Among the investigated CaRGs, patients with high levels of TRPV2 expression were characterized by a shorter overall survival. TRPV2 expression was found to increase according to tumor stage. Both mRNA and protein levels were significantly higher in tumor than normal stomach samples. TRPV2 was also associated with poor prognosis in the Lauren’s intestinal type GC and in patients treated with adjuvant therapy. Overall, we highlighted the relevance of TRPV2 not only as a prognostic biomarker but also as a potential therapeutic target to improve GC treatment efficacy. MDPI 2019-05-11 /pmc/articles/PMC6572141/ /pubmed/31083561 http://dx.doi.org/10.3390/jcm8050662 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zoppoli, Pietro
Calice, Giovanni
Laurino, Simona
Ruggieri, Vitalba
La Rocca, Francesco
La Torre, Giuseppe
Ciuffi, Mario
Amendola, Elena
De Vita, Ferdinando
Petrillo, Angelica
Napolitano, Giuliana
Falco, Geppino
Russi, Sabino
TRPV2 Calcium Channel Gene Expression and Outcomes in Gastric Cancer Patients: A Clinically Relevant Association
title TRPV2 Calcium Channel Gene Expression and Outcomes in Gastric Cancer Patients: A Clinically Relevant Association
title_full TRPV2 Calcium Channel Gene Expression and Outcomes in Gastric Cancer Patients: A Clinically Relevant Association
title_fullStr TRPV2 Calcium Channel Gene Expression and Outcomes in Gastric Cancer Patients: A Clinically Relevant Association
title_full_unstemmed TRPV2 Calcium Channel Gene Expression and Outcomes in Gastric Cancer Patients: A Clinically Relevant Association
title_short TRPV2 Calcium Channel Gene Expression and Outcomes in Gastric Cancer Patients: A Clinically Relevant Association
title_sort trpv2 calcium channel gene expression and outcomes in gastric cancer patients: a clinically relevant association
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572141/
https://www.ncbi.nlm.nih.gov/pubmed/31083561
http://dx.doi.org/10.3390/jcm8050662
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