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Upregulation of the alternative splicing factor NOVA2 in colorectal cancer vasculature
BACKGROUND: Tumor-specific isoforms generated by alternative splicing (AS) are demonstrated to contribute to tumor progression and can represent potential biomarkers. NOVA2 is an AS factor that in physiological conditions regulates endothelial cells’ (ECs) polarity and vessel lumen maturation, likel...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157992/ https://www.ncbi.nlm.nih.gov/pubmed/30275709 http://dx.doi.org/10.2147/OTT.S171678 |
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author | Gallo, Stefania Arcidiacono, Maria Vittoria Tisato, Veronica Piva, Roberta Penolazzi, Letizia Bosi, Cristina Feo, Carlo V Gafà, Roberta Secchiero, Paola |
author_facet | Gallo, Stefania Arcidiacono, Maria Vittoria Tisato, Veronica Piva, Roberta Penolazzi, Letizia Bosi, Cristina Feo, Carlo V Gafà, Roberta Secchiero, Paola |
author_sort | Gallo, Stefania |
collection | PubMed |
description | BACKGROUND: Tumor-specific isoforms generated by alternative splicing (AS) are demonstrated to contribute to tumor progression and can represent potential biomarkers. NOVA2 is an AS factor that in physiological conditions regulates endothelial cells’ (ECs) polarity and vessel lumen maturation, likely by mediating AS of apical–basal polarity regulators. However, NOVA2 expression in tumor ECs and its regulation have never been investigated. METHODS: To elucidate this, 40 colorectal cancer patients were enrolled and NOVA2 expression was investigated by immunohistochemistry in samples bearing both the normal mucosa and the tumor tissue. RESULTS: NOVA2 was found expressed in ECs of tumor vasculature and, importantly, it was upregulated in tumor ECs with respect to normal mucosa ECs in all cases (P<0.001). The same samples analyzed by immunohistochemistry for the expression HIF1α, a marker of hypoxia, showed a positive and significant association with NOVA2 levels (P=0.045). Of note, NOVA2 was upregulated by hypoxia also in an in vitro ECs model. CONCLUSION: Our results provide, for the first time, evidence of NOVA2 expression and upregulation in tumor ECs and highlight hypoxia as a potential regulatory factor. These findings open a completely new perspective to study tumor vasculature and to uncover NOVA2 as a potential source of biomarkers and therapeutic targets based on AS isoforms. |
format | Online Article Text |
id | pubmed-6157992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61579922018-10-01 Upregulation of the alternative splicing factor NOVA2 in colorectal cancer vasculature Gallo, Stefania Arcidiacono, Maria Vittoria Tisato, Veronica Piva, Roberta Penolazzi, Letizia Bosi, Cristina Feo, Carlo V Gafà, Roberta Secchiero, Paola Onco Targets Ther Original Research BACKGROUND: Tumor-specific isoforms generated by alternative splicing (AS) are demonstrated to contribute to tumor progression and can represent potential biomarkers. NOVA2 is an AS factor that in physiological conditions regulates endothelial cells’ (ECs) polarity and vessel lumen maturation, likely by mediating AS of apical–basal polarity regulators. However, NOVA2 expression in tumor ECs and its regulation have never been investigated. METHODS: To elucidate this, 40 colorectal cancer patients were enrolled and NOVA2 expression was investigated by immunohistochemistry in samples bearing both the normal mucosa and the tumor tissue. RESULTS: NOVA2 was found expressed in ECs of tumor vasculature and, importantly, it was upregulated in tumor ECs with respect to normal mucosa ECs in all cases (P<0.001). The same samples analyzed by immunohistochemistry for the expression HIF1α, a marker of hypoxia, showed a positive and significant association with NOVA2 levels (P=0.045). Of note, NOVA2 was upregulated by hypoxia also in an in vitro ECs model. CONCLUSION: Our results provide, for the first time, evidence of NOVA2 expression and upregulation in tumor ECs and highlight hypoxia as a potential regulatory factor. These findings open a completely new perspective to study tumor vasculature and to uncover NOVA2 as a potential source of biomarkers and therapeutic targets based on AS isoforms. Dove Medical Press 2018-09-20 /pmc/articles/PMC6157992/ /pubmed/30275709 http://dx.doi.org/10.2147/OTT.S171678 Text en © 2018 Gallo et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Gallo, Stefania Arcidiacono, Maria Vittoria Tisato, Veronica Piva, Roberta Penolazzi, Letizia Bosi, Cristina Feo, Carlo V Gafà, Roberta Secchiero, Paola Upregulation of the alternative splicing factor NOVA2 in colorectal cancer vasculature |
title | Upregulation of the alternative splicing factor NOVA2 in colorectal cancer vasculature |
title_full | Upregulation of the alternative splicing factor NOVA2 in colorectal cancer vasculature |
title_fullStr | Upregulation of the alternative splicing factor NOVA2 in colorectal cancer vasculature |
title_full_unstemmed | Upregulation of the alternative splicing factor NOVA2 in colorectal cancer vasculature |
title_short | Upregulation of the alternative splicing factor NOVA2 in colorectal cancer vasculature |
title_sort | upregulation of the alternative splicing factor nova2 in colorectal cancer vasculature |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6157992/ https://www.ncbi.nlm.nih.gov/pubmed/30275709 http://dx.doi.org/10.2147/OTT.S171678 |
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