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Biological Role and Aberrant Overexpression of Syntenin-1 in Cancer: Potential Role as a Biomarker and Therapeutic Target
Syntenin-1 is a 298 amino acid protein codified by the melanoma differentiation-associated gene-9 (MDA-9). Structurally, it is composed of four domains: N-terminal, PDZ1, PDZ2, and C-terminal. The PDZ domains of syntenin-1 are involved in the stability and interaction with other molecules such as pr...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135703/ https://www.ncbi.nlm.nih.gov/pubmed/37189651 http://dx.doi.org/10.3390/biomedicines11041034 |
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author | Pintor-Romero, Valeria Guadalupe Hurtado-Ortega, Edgar Nicolás-Morales, María Lilia Gutiérrez-Torres, Mayralina Vences-Velázquez, Amalia Ortuño-Pineda, Carlos Espinoza-Rojo, Mónica Navarro-Tito, Napoleón Cortés-Sarabia, Karen |
author_facet | Pintor-Romero, Valeria Guadalupe Hurtado-Ortega, Edgar Nicolás-Morales, María Lilia Gutiérrez-Torres, Mayralina Vences-Velázquez, Amalia Ortuño-Pineda, Carlos Espinoza-Rojo, Mónica Navarro-Tito, Napoleón Cortés-Sarabia, Karen |
author_sort | Pintor-Romero, Valeria Guadalupe |
collection | PubMed |
description | Syntenin-1 is a 298 amino acid protein codified by the melanoma differentiation-associated gene-9 (MDA-9). Structurally, it is composed of four domains: N-terminal, PDZ1, PDZ2, and C-terminal. The PDZ domains of syntenin-1 are involved in the stability and interaction with other molecules such as proteins, glycoproteins, and lipids. Domains are also associated with several biological functions such as the activation of signaling pathways related to cell-to-cell adhesion, signaling translation, and the traffic of intracellular lipids, among others. The overexpression of syntenin-1 has been reported in glioblastoma, colorectal, melanoma, lung, prostate, and breast cancer, which promotes tumorigenesis by regulating cell migration, invasion, proliferation, angiogenesis, apoptosis, and immune response evasion, and metastasis. The overexpression of syntenin-1 in samples has been associated with worst prognostic and recurrence, whereas the use of inhibitors such as shRNA, siRNA, and PDZli showed a diminution of the tumor size and reduction in metastasis and invasion. Syntenin-1 has been suggested as a potential biomarker and therapeutic target in cancer for developing more effective diagnostic/prognostic tests or passive/active immunotherapies. |
format | Online Article Text |
id | pubmed-10135703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101357032023-04-28 Biological Role and Aberrant Overexpression of Syntenin-1 in Cancer: Potential Role as a Biomarker and Therapeutic Target Pintor-Romero, Valeria Guadalupe Hurtado-Ortega, Edgar Nicolás-Morales, María Lilia Gutiérrez-Torres, Mayralina Vences-Velázquez, Amalia Ortuño-Pineda, Carlos Espinoza-Rojo, Mónica Navarro-Tito, Napoleón Cortés-Sarabia, Karen Biomedicines Review Syntenin-1 is a 298 amino acid protein codified by the melanoma differentiation-associated gene-9 (MDA-9). Structurally, it is composed of four domains: N-terminal, PDZ1, PDZ2, and C-terminal. The PDZ domains of syntenin-1 are involved in the stability and interaction with other molecules such as proteins, glycoproteins, and lipids. Domains are also associated with several biological functions such as the activation of signaling pathways related to cell-to-cell adhesion, signaling translation, and the traffic of intracellular lipids, among others. The overexpression of syntenin-1 has been reported in glioblastoma, colorectal, melanoma, lung, prostate, and breast cancer, which promotes tumorigenesis by regulating cell migration, invasion, proliferation, angiogenesis, apoptosis, and immune response evasion, and metastasis. The overexpression of syntenin-1 in samples has been associated with worst prognostic and recurrence, whereas the use of inhibitors such as shRNA, siRNA, and PDZli showed a diminution of the tumor size and reduction in metastasis and invasion. Syntenin-1 has been suggested as a potential biomarker and therapeutic target in cancer for developing more effective diagnostic/prognostic tests or passive/active immunotherapies. MDPI 2023-03-27 /pmc/articles/PMC10135703/ /pubmed/37189651 http://dx.doi.org/10.3390/biomedicines11041034 Text en © 2023 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 Pintor-Romero, Valeria Guadalupe Hurtado-Ortega, Edgar Nicolás-Morales, María Lilia Gutiérrez-Torres, Mayralina Vences-Velázquez, Amalia Ortuño-Pineda, Carlos Espinoza-Rojo, Mónica Navarro-Tito, Napoleón Cortés-Sarabia, Karen Biological Role and Aberrant Overexpression of Syntenin-1 in Cancer: Potential Role as a Biomarker and Therapeutic Target |
title | Biological Role and Aberrant Overexpression of Syntenin-1 in Cancer: Potential Role as a Biomarker and Therapeutic Target |
title_full | Biological Role and Aberrant Overexpression of Syntenin-1 in Cancer: Potential Role as a Biomarker and Therapeutic Target |
title_fullStr | Biological Role and Aberrant Overexpression of Syntenin-1 in Cancer: Potential Role as a Biomarker and Therapeutic Target |
title_full_unstemmed | Biological Role and Aberrant Overexpression of Syntenin-1 in Cancer: Potential Role as a Biomarker and Therapeutic Target |
title_short | Biological Role and Aberrant Overexpression of Syntenin-1 in Cancer: Potential Role as a Biomarker and Therapeutic Target |
title_sort | biological role and aberrant overexpression of syntenin-1 in cancer: potential role as a biomarker and therapeutic target |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10135703/ https://www.ncbi.nlm.nih.gov/pubmed/37189651 http://dx.doi.org/10.3390/biomedicines11041034 |
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