Hypoxia-induced alternative splicing: the 11th Hallmark of Cancer
Abstract Hypoxia-induced alternative splicing is a potent driving force in tumour pathogenesis and progression. In this review, we update currents concepts of hypoxia-induced alternative splicing and how it influences tumour biology. Following brief descriptions of tumour-associated hypoxia and the...
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doaj-fc7c3e84f72346c69f22decada05cac62020-11-25T03:59:22ZengBMCJournal of Experimental & Clinical Cancer Research1756-99662020-06-0139113010.1186/s13046-020-01616-9Hypoxia-induced alternative splicing: the 11th Hallmark of CancerAntonietta Rosella Farina0Lucia Cappabianca1Michela Sebastiano2Veronica Zelli3Stefano Guadagni4Andrew Reay Mackay5Department of Applied Clinical and Biotechnological Sciences, University of L’AquilaDepartment of Applied Clinical and Biotechnological Sciences, University of L’AquilaDepartment of Applied Clinical and Biotechnological Sciences, University of L’AquilaDepartment of Applied Clinical and Biotechnological Sciences, University of L’AquilaDepartment of Applied Clinical and Biotechnological Sciences, University of L’AquilaDepartment of Applied Clinical and Biotechnological Sciences, University of L’AquilaAbstract Hypoxia-induced alternative splicing is a potent driving force in tumour pathogenesis and progression. In this review, we update currents concepts of hypoxia-induced alternative splicing and how it influences tumour biology. Following brief descriptions of tumour-associated hypoxia and the pre-mRNA splicing process, we review the many ways hypoxia regulates alternative splicing and how hypoxia-induced alternative splicing impacts each individual hallmark of cancer. Hypoxia-induced alternative splicing integrates chemical and cellular tumour microenvironments, underpins continuous adaptation of the tumour cellular microenvironment responsible for metastatic progression and plays clear roles in oncogene activation and autonomous tumour growth, tumor suppressor inactivation, tumour cell immortalization, angiogenesis, tumour cell evasion of programmed cell death and the anti-tumour immune response, a tumour-promoting inflammatory response, adaptive metabolic re-programming, epithelial to mesenchymal transition, invasion and genetic instability, all of which combine to promote metastatic disease. The impressive number of hypoxia-induced alternative spliced protein isoforms that characterize tumour progression, classifies hypoxia-induced alternative splicing as the 11th hallmark of cancer, and offers a fertile source of potential diagnostic/prognostic markers and therapeutic targets.http://link.springer.com/article/10.1186/s13046-020-01616-9HypoxiaAlternative splicingCancer hallmarks |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Antonietta Rosella Farina Lucia Cappabianca Michela Sebastiano Veronica Zelli Stefano Guadagni Andrew Reay Mackay |
spellingShingle |
Antonietta Rosella Farina Lucia Cappabianca Michela Sebastiano Veronica Zelli Stefano Guadagni Andrew Reay Mackay Hypoxia-induced alternative splicing: the 11th Hallmark of Cancer Journal of Experimental & Clinical Cancer Research Hypoxia Alternative splicing Cancer hallmarks |
author_facet |
Antonietta Rosella Farina Lucia Cappabianca Michela Sebastiano Veronica Zelli Stefano Guadagni Andrew Reay Mackay |
author_sort |
Antonietta Rosella Farina |
title |
Hypoxia-induced alternative splicing: the 11th Hallmark of Cancer |
title_short |
Hypoxia-induced alternative splicing: the 11th Hallmark of Cancer |
title_full |
Hypoxia-induced alternative splicing: the 11th Hallmark of Cancer |
title_fullStr |
Hypoxia-induced alternative splicing: the 11th Hallmark of Cancer |
title_full_unstemmed |
Hypoxia-induced alternative splicing: the 11th Hallmark of Cancer |
title_sort |
hypoxia-induced alternative splicing: the 11th hallmark of cancer |
publisher |
BMC |
series |
Journal of Experimental & Clinical Cancer Research |
issn |
1756-9966 |
publishDate |
2020-06-01 |
description |
Abstract Hypoxia-induced alternative splicing is a potent driving force in tumour pathogenesis and progression. In this review, we update currents concepts of hypoxia-induced alternative splicing and how it influences tumour biology. Following brief descriptions of tumour-associated hypoxia and the pre-mRNA splicing process, we review the many ways hypoxia regulates alternative splicing and how hypoxia-induced alternative splicing impacts each individual hallmark of cancer. Hypoxia-induced alternative splicing integrates chemical and cellular tumour microenvironments, underpins continuous adaptation of the tumour cellular microenvironment responsible for metastatic progression and plays clear roles in oncogene activation and autonomous tumour growth, tumor suppressor inactivation, tumour cell immortalization, angiogenesis, tumour cell evasion of programmed cell death and the anti-tumour immune response, a tumour-promoting inflammatory response, adaptive metabolic re-programming, epithelial to mesenchymal transition, invasion and genetic instability, all of which combine to promote metastatic disease. The impressive number of hypoxia-induced alternative spliced protein isoforms that characterize tumour progression, classifies hypoxia-induced alternative splicing as the 11th hallmark of cancer, and offers a fertile source of potential diagnostic/prognostic markers and therapeutic targets. |
topic |
Hypoxia Alternative splicing Cancer hallmarks |
url |
http://link.springer.com/article/10.1186/s13046-020-01616-9 |
work_keys_str_mv |
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