Pan-cancer analysis of the prognostic and immunological role of matrix metalloproteinase 9.


Journal

Medicine
ISSN: 1536-5964
Titre abrégé: Medicine (Baltimore)
Pays: United States
ID NLM: 2985248R

Informations de publication

Date de publication:
28 Jul 2023
Historique:
medline: 31 7 2023
pubmed: 28 7 2023
entrez: 28 7 2023
Statut: ppublish

Résumé

Matrix metalloproteinase 9 (MMP9), a zinc ion-dependent endopeptidase, is one of the most complex matrix metalloproteinases in the gelatinase family. During tissue remodeling, MMP9 leads to gelatin and collagen degradation, which in turn promotes tumor invasion and metastasis. However, comprehensive pan-cancer analysis has not been performed for MMP9. In addition, the diagnostic and prognostic value of MMP9 as a cancer biomarker remain poorly understood, as well as the utility of MMP9 expression as a predictor of immunological responses. Based on a comprehensive analysis of bioinformatics information, we investigated MMP9 expression in different cancers, correlations between MMP9 expression and cancer prognosis and gene mutations, and relationships between MMP9 expression and immune cell infiltration. Our results indicated that MMP9 was highly expressed in most malignant cancers. MMP9 expression was significantly positively or negatively associated with the clinical prognoses of patients with different kinds of cancer. Furthermore, MMP9 expression significantly correlated with infiltrating cells and the expression levels of immune checkpoint genes. This pan-cancer analysis provides comprehensive information on the potential value of MMP9 as a theranostic biomarker.

Identifiants

pubmed: 37505149
doi: 10.1097/MD.0000000000034499
pii: 00005792-202307280-00032
pmc: PMC10378727
doi:

Substances chimiques

Matrix Metalloproteinase 9 EC 3.4.24.35

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e34499

Informations de copyright

Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc.

Déclaration de conflit d'intérêts

The authors have no funding and conflicts of interest to disclose.

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Auteurs

Jie Zhang (J)

Clinical Medical School, Chengdu Medical College, Chengdu, China.
Oncology Department, The First Affiliated Hospital of Chengdu Medical College, Chengdu, China.
Key Clinical Specialty of Sichuan Province (Oncology Department), The First Affiliated Hospital of Chengdu Medical College, Chengdu, China.

Lei Xu (L)

Clinical Medical School, Chengdu Medical College, Chengdu, China.
Gynecology Department, The First Affiliated Hospital of Chengdu Medical College, Chengdu, China.

Jingjun Zhang (J)

Oncology Department, The People's Hospital of Jianyang City, Chengdu, China.

Ying Liu (Y)

Clinical Medical School, Chengdu Medical College, Chengdu, China.

Xiang Li (X)

Clinical Medical School, Chengdu Medical College, Chengdu, China.

Tao Ren (T)

Clinical Medical School, Chengdu Medical College, Chengdu, China.
Oncology Department, The First Affiliated Hospital of Chengdu Medical College, Chengdu, China.
Key Clinical Specialty of Sichuan Province (Oncology Department), The First Affiliated Hospital of Chengdu Medical College, Chengdu, China.

Hairong Liu (H)

Clinical Medical School, Chengdu Medical College, Chengdu, China.
Science and Technology Department, The First Affiliated Hospital of Chengdu Medical College, Chengdu, China.

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