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pmid:31024988

Matrix Metalloproteinase 11 Is a Potential Therapeutic Target in Lung Adenocarcinoma.

Haoran Yang · Peng Jiang · Dongyan Liu · Hong-Qiang Wang · Qingmei Deng · Xiaojie Niu · Li Lu · Haiming Dai · Hongzhi Wang · Wulin Yang

Molecular therapy oncolytics · 2019 doi:10.1016/j.omto.2019.03.012

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Data

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Matrix Metalloproteinase 11 Is a Potential Therapeutic Target in Lung Adenocarcinoma.
doi
10.1016/j.omto.2019.03.012
pmid
31024988
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Haoran Yang
[1]
Peng Jiang
[2]
Dongyan Liu
[3]
Hong-Qiang Wang
[4]
Qingmei Deng
[5]
Xiaojie Niu
[6]
Li Lu
[7]
Haiming Dai
[8]
Hongzhi Wang
[9]
Wulin Yang
journal
Molecular therapy oncolytics
year
2019
abstract
Lung cancer is one of the leading causes of cancer-associated death, with the etiology largely unknown. The aim of this study was to identify key driver genes with therapeutic potentials in lung adenocarcinoma (LUAD). Transcriptome microarray data from four GEO datasets (GEO: GSE7670, GSE10072, GSE68465, and GSE43458) were jointly analyzed for differentially expressed genes (DEGs). Ontologic analysis showed that most of the upregulated DEGs enriched in collagen catabolic and fibril organization processes were regulated by matrix metalloproteinases (MMPs). Matrix metalloproteinase 11 (MMP11), the highest upregulated MMP family member in LUAD-transformed cells, acted in an autocrine manner and was significantly increased in sera of LUAD patients. MMP11 depletion severely impaired LUAD cell proliferation, migration, and invasion in vitro, in line with retarded tumor growth in xenograft models. Treatment of different human LUAD cell lines with anti-MMP11 antibody significantly retarded cell growth and migration. Administration of anti-MMP11 antibody at a dose of 1 μg/g body weight significantly suppressed tumor growth in xenograft models. These findings indicate that MMP11 is a key cancer driver gene in LUAD and is an appealing target for antibody therapy.
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Homo sapiens
title
caArray_jacob-00182: Gene expression-based survival prediction in lung adenocarcinoma: a multi-site, blinded validation study
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2026-11-01T15:39:55Z
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Four gene expression datasets of LUAD in the GEO database, including GSE7670, GSE10072, GSE68465, and GSE43458, were used for identification of genes differentially expressed in lung cancer.
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Expression data from Lung cancer
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2026-11-01T15:14:33Z
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identifier_resolution_only_no_download_no_licence_read
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Common DEGs Identified in Lung Adenocarcinoma
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Bioinformatics Identifies DEGs in LUAD and Non-malignant Tissues
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Common DEGs Identified in Lung Adenocarcinoma
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The paper names GSE7670, GSE10072, GSE68465 in GEO and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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in lung adenocarcinoma (LUAD). Transcriptome microarray data from four GEO datasets (GEO: GSE7670, G
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The aim of this study was to identify key driver genes with therapeutic potentials in lung adenocarcinoma (LUAD). Transcriptome microarray data from four GEO datasets (GEO: GSE7670, GSE10072, GSE68465, and GSE43458) were jointly analyzed for differentially expressed genes (DEGs). Ontologic analysis showed that most of the upregulated DEGs enriched in collagen catabolic and fibril organization processes were regulated by matrix metalloproteinases (MMPs). Matrix metalloproteinase 11 (MMP11), the highest upregulated MMP family member in LUAD-transformed cells, acted in an autocrine manner and was significantly increased in sera of LUAD patients. MMP11 depletion severely impaired LUAD cell proliferation, migration, and invasion in vitro, in line with retarded tumor growth in xenograft models. Treatment of different human LUAD cell lines with anti-MMP11 antibody significantly retarded cell growth and migration. 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