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Tropomyosins: Potential Biomarkers for Urothelial Bladder Cancer

Despite the incidence and prevalence of urothelial bladder cancer (UBC), few advances in treatment and diagnosis have been made in recent years. In this review, we discuss potential biomarker candidates: the tropomyosin family of genes, encoded by four loci in the human genome. The expression of the...

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Autores principales: Humayun-Zakaria, Nada, Arnold, Roland, Goel, Anshita, Ward, Douglas, Savill, Stuart, Bryan, Richard T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429115/
https://www.ncbi.nlm.nih.gov/pubmed/30836651
http://dx.doi.org/10.3390/ijms20051102
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author Humayun-Zakaria, Nada
Arnold, Roland
Goel, Anshita
Ward, Douglas
Savill, Stuart
Bryan, Richard T.
author_facet Humayun-Zakaria, Nada
Arnold, Roland
Goel, Anshita
Ward, Douglas
Savill, Stuart
Bryan, Richard T.
author_sort Humayun-Zakaria, Nada
collection PubMed
description Despite the incidence and prevalence of urothelial bladder cancer (UBC), few advances in treatment and diagnosis have been made in recent years. In this review, we discuss potential biomarker candidates: the tropomyosin family of genes, encoded by four loci in the human genome. The expression of these genes is tissue-specific. Tropomyosins are responsible for diverse cellular roles, most notably based upon their interplay with actin to maintain cellular processes, integrity and structure. Tropomyosins exhibit a large variety of splice forms, and altered isoform expression levels have been associated with cancer, including UBC. Notably, tropomyosin isoforms are detectable in urine, offering the potential for non-invasive diagnosis and risk-stratification. This review collates the basic knowledge on tropomyosin and its isoforms, and discusses their relationships with cancer-related phenomena, most specifically in UBC.
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spelling pubmed-64291152019-04-10 Tropomyosins: Potential Biomarkers for Urothelial Bladder Cancer Humayun-Zakaria, Nada Arnold, Roland Goel, Anshita Ward, Douglas Savill, Stuart Bryan, Richard T. Int J Mol Sci Review Despite the incidence and prevalence of urothelial bladder cancer (UBC), few advances in treatment and diagnosis have been made in recent years. In this review, we discuss potential biomarker candidates: the tropomyosin family of genes, encoded by four loci in the human genome. The expression of these genes is tissue-specific. Tropomyosins are responsible for diverse cellular roles, most notably based upon their interplay with actin to maintain cellular processes, integrity and structure. Tropomyosins exhibit a large variety of splice forms, and altered isoform expression levels have been associated with cancer, including UBC. Notably, tropomyosin isoforms are detectable in urine, offering the potential for non-invasive diagnosis and risk-stratification. This review collates the basic knowledge on tropomyosin and its isoforms, and discusses their relationships with cancer-related phenomena, most specifically in UBC. MDPI 2019-03-04 /pmc/articles/PMC6429115/ /pubmed/30836651 http://dx.doi.org/10.3390/ijms20051102 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 Review
Humayun-Zakaria, Nada
Arnold, Roland
Goel, Anshita
Ward, Douglas
Savill, Stuart
Bryan, Richard T.
Tropomyosins: Potential Biomarkers for Urothelial Bladder Cancer
title Tropomyosins: Potential Biomarkers for Urothelial Bladder Cancer
title_full Tropomyosins: Potential Biomarkers for Urothelial Bladder Cancer
title_fullStr Tropomyosins: Potential Biomarkers for Urothelial Bladder Cancer
title_full_unstemmed Tropomyosins: Potential Biomarkers for Urothelial Bladder Cancer
title_short Tropomyosins: Potential Biomarkers for Urothelial Bladder Cancer
title_sort tropomyosins: potential biomarkers for urothelial bladder cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429115/
https://www.ncbi.nlm.nih.gov/pubmed/30836651
http://dx.doi.org/10.3390/ijms20051102
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