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Plectin in Cancer: From Biomarker to Therapeutic Target
The cytolinker and scaffolding protein, plectin, has emerged as a potent driver of malignant hallmarks in many human cancers due to its involvement in various cellular activities contributing to tumorigenesis, including cancer cell proliferation, adhesion, migration, invasion, and signal transductio...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469460/ https://www.ncbi.nlm.nih.gov/pubmed/34571895 http://dx.doi.org/10.3390/cells10092246 |
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author | Perez, Samantha M. Brinton, Lindsey T. Kelly, Kimberly A. |
author_facet | Perez, Samantha M. Brinton, Lindsey T. Kelly, Kimberly A. |
author_sort | Perez, Samantha M. |
collection | PubMed |
description | The cytolinker and scaffolding protein, plectin, has emerged as a potent driver of malignant hallmarks in many human cancers due to its involvement in various cellular activities contributing to tumorigenesis, including cancer cell proliferation, adhesion, migration, invasion, and signal transduction. Evidence shows that beyond plectin’s diverse protein interactome, its cancer-specific mislocalization to the cell surface enables its function as a potent oncoprotein. As such, therapeutic targeting of plectin, its protein interactors, and, in particular, cancer-specific plectin (CSP) presents an attractive opportunity to impede carcinogenesis directly. Here, we report on plectin’s differential gene and protein expression in cancer, explore its mutational profile, and discuss the current understanding of plectin’s and CSP’s biological function in cancer. Moreover, we review the landscape of plectin as a prognostic marker, diagnostic biomarker, and target for imaging and therapeutic modalities. We highlight how, beyond their respective biological importance, plectin’s common overexpression in cancer and CSP’s cancer-specific bioavailability underscore their potential as high-value druggable targets. We discuss how recent evidence of the potent anti-cancer effects of CSP therapeutic targeting opens the door for cell-surface mislocalized proteins as novel therapeutic targets. |
format | Online Article Text |
id | pubmed-8469460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84694602021-09-27 Plectin in Cancer: From Biomarker to Therapeutic Target Perez, Samantha M. Brinton, Lindsey T. Kelly, Kimberly A. Cells Review The cytolinker and scaffolding protein, plectin, has emerged as a potent driver of malignant hallmarks in many human cancers due to its involvement in various cellular activities contributing to tumorigenesis, including cancer cell proliferation, adhesion, migration, invasion, and signal transduction. Evidence shows that beyond plectin’s diverse protein interactome, its cancer-specific mislocalization to the cell surface enables its function as a potent oncoprotein. As such, therapeutic targeting of plectin, its protein interactors, and, in particular, cancer-specific plectin (CSP) presents an attractive opportunity to impede carcinogenesis directly. Here, we report on plectin’s differential gene and protein expression in cancer, explore its mutational profile, and discuss the current understanding of plectin’s and CSP’s biological function in cancer. Moreover, we review the landscape of plectin as a prognostic marker, diagnostic biomarker, and target for imaging and therapeutic modalities. We highlight how, beyond their respective biological importance, plectin’s common overexpression in cancer and CSP’s cancer-specific bioavailability underscore their potential as high-value druggable targets. We discuss how recent evidence of the potent anti-cancer effects of CSP therapeutic targeting opens the door for cell-surface mislocalized proteins as novel therapeutic targets. MDPI 2021-08-30 /pmc/articles/PMC8469460/ /pubmed/34571895 http://dx.doi.org/10.3390/cells10092246 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Perez, Samantha M. Brinton, Lindsey T. Kelly, Kimberly A. Plectin in Cancer: From Biomarker to Therapeutic Target |
title | Plectin in Cancer: From Biomarker to Therapeutic Target |
title_full | Plectin in Cancer: From Biomarker to Therapeutic Target |
title_fullStr | Plectin in Cancer: From Biomarker to Therapeutic Target |
title_full_unstemmed | Plectin in Cancer: From Biomarker to Therapeutic Target |
title_short | Plectin in Cancer: From Biomarker to Therapeutic Target |
title_sort | plectin in cancer: from biomarker to therapeutic target |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8469460/ https://www.ncbi.nlm.nih.gov/pubmed/34571895 http://dx.doi.org/10.3390/cells10092246 |
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