Cargando…
Molecular Mechanisms Driven by MT4-MMP in Cancer Progression
MT4-MMP (or MMP-17) belongs to the membrane-type matrix metalloproteinases (MT-MMPs), a distinct subset of the MMP family that is anchored to the cell surface, in this case by a glycosylphosphatidylinositol (GPI) motif. Its expression in a variety of cancers is well documented. However, the molecula...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298049/ https://www.ncbi.nlm.nih.gov/pubmed/37373092 http://dx.doi.org/10.3390/ijms24129944 |
_version_ | 1785064019381452800 |
---|---|
author | Muñoz-Sáez, Emma Moracho, Natalia Learte, Ana I. R. Collignon, Alice Arroyo, Alicia G. Noel, Agnés Sounni, Nor Eddine Sánchez-Camacho, Cristina |
author_facet | Muñoz-Sáez, Emma Moracho, Natalia Learte, Ana I. R. Collignon, Alice Arroyo, Alicia G. Noel, Agnés Sounni, Nor Eddine Sánchez-Camacho, Cristina |
author_sort | Muñoz-Sáez, Emma |
collection | PubMed |
description | MT4-MMP (or MMP-17) belongs to the membrane-type matrix metalloproteinases (MT-MMPs), a distinct subset of the MMP family that is anchored to the cell surface, in this case by a glycosylphosphatidylinositol (GPI) motif. Its expression in a variety of cancers is well documented. However, the molecular mechanisms by which MT4-MMP contributes to tumor development need further investigation. In this review, we aim to summarize the contribution of MT4-MMP in tumorigenesis, focusing on the molecular mechanisms triggered by the enzyme in tumor cell migration, invasiveness, and proliferation, in the tumor vasculature and microenvironment, as well as during metastasis. In particular, we highlight the putative substrates processed and signaling cascades activated by MT4-MMP that may underlie these malignancy processes and compare this with what is known about its role during embryonic development. Finally, MT4-MMP is a relevant biomarker of malignancy that can be used for monitoring cancer progression in patients as well as a potential target for future therapeutic drug development. |
format | Online Article Text |
id | pubmed-10298049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102980492023-06-28 Molecular Mechanisms Driven by MT4-MMP in Cancer Progression Muñoz-Sáez, Emma Moracho, Natalia Learte, Ana I. R. Collignon, Alice Arroyo, Alicia G. Noel, Agnés Sounni, Nor Eddine Sánchez-Camacho, Cristina Int J Mol Sci Review MT4-MMP (or MMP-17) belongs to the membrane-type matrix metalloproteinases (MT-MMPs), a distinct subset of the MMP family that is anchored to the cell surface, in this case by a glycosylphosphatidylinositol (GPI) motif. Its expression in a variety of cancers is well documented. However, the molecular mechanisms by which MT4-MMP contributes to tumor development need further investigation. In this review, we aim to summarize the contribution of MT4-MMP in tumorigenesis, focusing on the molecular mechanisms triggered by the enzyme in tumor cell migration, invasiveness, and proliferation, in the tumor vasculature and microenvironment, as well as during metastasis. In particular, we highlight the putative substrates processed and signaling cascades activated by MT4-MMP that may underlie these malignancy processes and compare this with what is known about its role during embryonic development. Finally, MT4-MMP is a relevant biomarker of malignancy that can be used for monitoring cancer progression in patients as well as a potential target for future therapeutic drug development. MDPI 2023-06-09 /pmc/articles/PMC10298049/ /pubmed/37373092 http://dx.doi.org/10.3390/ijms24129944 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 Muñoz-Sáez, Emma Moracho, Natalia Learte, Ana I. R. Collignon, Alice Arroyo, Alicia G. Noel, Agnés Sounni, Nor Eddine Sánchez-Camacho, Cristina Molecular Mechanisms Driven by MT4-MMP in Cancer Progression |
title | Molecular Mechanisms Driven by MT4-MMP in Cancer Progression |
title_full | Molecular Mechanisms Driven by MT4-MMP in Cancer Progression |
title_fullStr | Molecular Mechanisms Driven by MT4-MMP in Cancer Progression |
title_full_unstemmed | Molecular Mechanisms Driven by MT4-MMP in Cancer Progression |
title_short | Molecular Mechanisms Driven by MT4-MMP in Cancer Progression |
title_sort | molecular mechanisms driven by mt4-mmp in cancer progression |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298049/ https://www.ncbi.nlm.nih.gov/pubmed/37373092 http://dx.doi.org/10.3390/ijms24129944 |
work_keys_str_mv | AT munozsaezemma molecularmechanismsdrivenbymt4mmpincancerprogression AT morachonatalia molecularmechanismsdrivenbymt4mmpincancerprogression AT learteanair molecularmechanismsdrivenbymt4mmpincancerprogression AT collignonalice molecularmechanismsdrivenbymt4mmpincancerprogression AT arroyoaliciag molecularmechanismsdrivenbymt4mmpincancerprogression AT noelagnes molecularmechanismsdrivenbymt4mmpincancerprogression AT sounninoreddine molecularmechanismsdrivenbymt4mmpincancerprogression AT sanchezcamachocristina molecularmechanismsdrivenbymt4mmpincancerprogression |