MMP11 as a prognostic biomarker correlated with immune infiltrates in pancreatic adenocarcinoma
Matrix metalloproteinase 11 ( ) plays a vital role in cell proliferation, apoptosis, tumor angiogenesis, migration, and other basic processes. Currently, few studies have examined the value of MMP11 in pancreatic cancer in relation to prognostic risk, diagnostic indicators, and immunotherapy. This s...
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Veröffentlicht in: | Journal of gastrointestinal oncology 2024-06, Vol.15 (3), p.1224-1244 |
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Sprache: | eng |
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Zusammenfassung: | Matrix metalloproteinase 11 (
) plays a vital role in cell proliferation, apoptosis, tumor angiogenesis, migration, and other basic processes. Currently, few studies have examined the value of MMP11 in pancreatic cancer in relation to prognostic risk, diagnostic indicators, and immunotherapy. This study aims to explore the association between
and the tumor immune microenvironment in pancreatic adenocarcinoma (PAAD).
We selected clinical samples and data downloaded from The Cancer Genome Atlas and Genotype-Tissue Expression, in addition, we use other online data for further analysis. Through a comprehensive bioinformatics investigation, we systematically analyzed the clinical significance and expression level of
in pancreatic cancer.
was overexpressed in many cancers, and a higher expression of
was associated with a poorer prognosis in pancreatic cancer. Conversely, the hypermethylation of
was associated with better overall survival. The
expression network had widespread effects on the prognosis and immune activation of PAAD. The expression of
was significantly associated with a variety of tumor-infiltrating immune cells. An association was also found between
expression and chemokines in PAAD. High
expression might be involved in immune cell migration to the tumor microenvironment.
MMP11 is a prognostic biomarker for patients in pancreatic cancer and may regulate the tumor immune microenvironment. The potential effects and mechanisms of
in PAAD require further exploring. |
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ISSN: | 2078-6891 2219-679X |
DOI: | 10.21037/jgo-24-425 |