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MT4-MMP 驱动的癌症进展中的分子机制。

Molecular Mechanisms Driven by MT4-MMP in Cancer Progression.

机构信息

Department of Health Science, School of Biomedical Sciences, Universidad Europea de Madrid, Villaviciosa de Odón, 28670 Madrid, Spain.

Department of Medicine, School of Biomedical Sciences, Universidad Europea de Madrid, Villaviciosa de Odón, 28670 Madrid, Spain.

出版信息

Int J Mol Sci. 2023 Jun 9;24(12):9944. doi: 10.3390/ijms24129944.


DOI:10.3390/ijms24129944
PMID:37373092
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10298049/
Abstract

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.

摘要

MT4-MMP(或 MMP-17)属于膜型基质金属蛋白酶(MT-MMPs),是 MMP 家族的一个独特亚群,通过糖基磷脂酰肌醇(GPI)基序锚定在细胞表面,在这种情况下。它在各种癌症中的表达已有充分记录。然而,MT4-MMP 促进肿瘤发展的分子机制仍需要进一步研究。在这篇综述中,我们旨在总结 MT4-MMP 在肿瘤发生中的作用,重点讨论酶在肿瘤细胞迁移、侵袭和增殖、肿瘤血管和微环境以及转移过程中触发的分子机制。特别是,我们强调了 MT4-MMP 处理的假定底物和激活的信号级联,这些可能是这些恶性过程的基础,并将其与已知的胚胎发育过程进行比较。最后,MT4-MMP 是一种与恶性相关的生物标志物,可用于监测患者的癌症进展,也是未来治疗性药物开发的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e11/10298049/98f901c0ef8a/ijms-24-09944-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e11/10298049/98f901c0ef8a/ijms-24-09944-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e11/10298049/98f901c0ef8a/ijms-24-09944-g001.jpg

相似文献

[1]
Molecular Mechanisms Driven by MT4-MMP in Cancer Progression.

Int J Mol Sci. 2023-6-9

[2]
MT4-MMP: The GPI-Anchored Membrane-Type Matrix Metalloprotease with Multiple Functions in Diseases.

Int J Mol Sci. 2019-1-16

[3]
Expression and Characterization of Membrane-Type 4 Matrix Metalloproteinase (MT4-MMP) and its Different Forms in Melanoma.

Cell Physiol Biochem. 2017

[4]
Developmental expression of membrane type 4-matrix metalloproteinase (Mt4-mmp/Mmp17) in the mouse embryo.

PLoS One. 2017-9-19

[5]
Regulation of membrane-type 4 matrix metalloproteinase by SLUG contributes to hypoxia-mediated metastasis.

Neoplasia. 2009-12

[6]
MT4-(MMP17) and MT6-MMP (MMP25), A unique set of membrane-anchored matrix metalloproteinases: properties and expression in cancer.

Cancer Metastasis Rev. 2008-6

[7]
Characterization of the dimerization interface of membrane type 4 (MT4)-matrix metalloproteinase.

J Biol Chem. 2011-8-2

[8]
The proteolytic activity of MT4-MMP is required for its pro-angiogenic and pro-metastatic promoting effects.

Int J Cancer. 2012-4-4

[9]
Membrane type 4 matrix metalloproteinase (MT4-MMP, MMP-17) is a glycosylphosphatidylinositol-anchored proteinase.

J Biol Chem. 1999-11-26

[10]
Membrane-type 4 matrix metalloproteinase (MT4-MMP) modulates water homeostasis in mice.

PLoS One. 2011-2-11

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[2]
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Cancer Immunol Immunother. 2025-5-26

[3]
Stage-Specific Tumoral Gene Expression Profiles of Black and White Patients with Colon Cancer.

Ann Surg Oncol. 2025-2

[4]
Identification and validation of matrix metalloproteinase hub genes as potential biomarkers for Skin Cutaneous Melanoma.

Front Oncol. 2024-10-18

[5]
SH3GL2 and MMP17 as lung adenocarcinoma biomarkers: a machine-learning based approach.

Biochem Biophys Rep. 2024-3-25

[6]
Recent Updates on the Therapeutic Prospects of Reversion-Inducing Cysteine-Rich Protein with Kazal Motifs (RECK) in Liver Injuries.

Int J Mol Sci. 2023-12-12

本文引用的文献

[1]
p38 MAPK priming boosts VSMC proliferation and arteriogenesis by promoting PGC1α-dependent mitochondrial dynamics.

Sci Rep. 2022-4-8

[2]
Smooth muscle-specific MMP17 (MT4-MMP) regulates the intestinal stem cell niche and regeneration after damage.

Nat Commun. 2021-11-18

[3]
Cargo-specific recruitment in clathrin- and dynamin-independent endocytosis.

Nat Cell Biol. 2021-10

[4]
Emerging roles of MT-MMPs in embryonic development.

Dev Dyn. 2022-2

[5]
How Single-Molecule Localization Microscopy Expanded Our Mechanistic Understanding of RNA Polymerase II Transcription.

Int J Mol Sci. 2021-6-22

[6]
MT4-MMP in tumor-associated macrophages is linked to hepatocellular carcinoma aggressiveness and recurrence.

Clin Transl Med. 2020-8

[7]
Neoplastic Cells are the Major Source of MT-MMPs in -Mutant Glioma, Thus Enhancing Tumor-Cell Intrinsic Brain Infiltration.

Cancers (Basel). 2020-8-29

[8]
Regulation of MT1-MMP Activity through Its Association with ERMs.

Cells. 2020-2-3

[9]
Role of Matrix Metalloproteinases in Angiogenesis and Cancer.

Front Oncol. 2019-12-6

[10]
MT4-MMP promotes invadopodia formation and cell motility in FaDu head and neck cancer cells.

Biochem Biophys Res Commun. 2019-12-5

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