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Dissecting the MUC5AC/ANXA2 signaling axis: implications for brain metastasis in lung adenocarcinoma.
- Source :
-
Experimental & molecular medicine [Exp Mol Med] 2024 Jun; Vol. 56 (6), pp. 1450-1460. Date of Electronic Publication: 2024 Jun 03. - Publication Year :
- 2024
-
Abstract
- Non-small cell lung carcinoma (NSCLC) exhibits a heightened propensity for brain metastasis, posing a significant clinical challenge. Mucin 5ac (MUC5AC) plays a pivotal role in the development of lung adenocarcinoma (LUAD); however, its role in causing brain metastases remains unknown. In this study, we aimed to investigate the contribution of MUC5AC to brain metastasis in patients with LUAD utilizing various brain metastasis models. Our findings revealed a substantial increase in the MUC5AC level in LUAD brain metastases (LUAD-BrM) samples and brain-tropic cell lines compared to primary samples or parental control cell lines. Intriguingly, depletion of MUC5AC in brain-tropic cells led to significant reductions in intracranial metastasis and tumor growth, and improved survival following intracardiac injection, in contrast to the observations in the control groups. Proteomic analysis revealed that mechanistically, MUC5AC depletion resulted in decreased expression of metastasis-associated molecules. There were increases in epithelial-to-mesenchymal transition, tumor invasiveness, and metastasis phenotypes in tumors with high MUC5AC expression. Furthermore, immunoprecipitation and proteomic analysis revealed a novel interaction of MUC5AC with Annexin A2 (ANXA2), which activated downstream matrix metalloproteases and facilitated extracellular matrix degradation to promote metastasis. Disrupting MUC5AC-ANXA2 signaling with a peptide inhibitor effectively abrogated the metastatic process. Additionally, treatment of tumor cells with an astrocyte-conditioned medium or the chemokine CCL2 resulted in upregulation of MUC5AC expression and enhanced brain colonization. In summary, our study demonstrates that the MUC5AC/ANXA2 signaling axis promotes brain metastasis, suggesting a potential therapeutic paradigm for LUAD patients with high MUC5AC expression.<br /> (© 2024. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.)
- Subjects :
- Humans
Animals
Cell Line, Tumor
Mice
Epithelial-Mesenchymal Transition genetics
Gene Expression Regulation, Neoplastic
Female
Mucin 5AC metabolism
Mucin 5AC genetics
Signal Transduction
Brain Neoplasms secondary
Brain Neoplasms metabolism
Brain Neoplasms pathology
Adenocarcinoma of Lung metabolism
Adenocarcinoma of Lung pathology
Adenocarcinoma of Lung genetics
Lung Neoplasms metabolism
Lung Neoplasms pathology
Lung Neoplasms secondary
Lung Neoplasms genetics
Annexin A2 metabolism
Annexin A2 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2092-6413
- Volume :
- 56
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Experimental & molecular medicine
- Publication Type :
- Academic Journal
- Accession number :
- 38825648
- Full Text :
- https://doi.org/10.1038/s12276-024-01255-6