Major Vault Protein (MVP) Associated With Mutation Is an Immune Microenvironment-Related Biomarker Promoting the Progression of Papillary Thyroid Cancer MAPK/ERK and PI3K/AKT Pathways.
Papillary thyroid cancer (PTC) is the most common malignancy of the endocrine system, with an increase in incidence frequency.
APA
Dong X, Akuetteh PDP, et al. (2021). Major Vault Protein (MVP) Associated With Mutation Is an Immune Microenvironment-Related Biomarker Promoting the Progression of Papillary Thyroid Cancer MAPK/ERK and PI3K/AKT Pathways.. Frontiers in cell and developmental biology, 9, 688370. https://doi.org/10.3389/fcell.2021.688370
MLA
Dong X, et al.. "Major Vault Protein (MVP) Associated With Mutation Is an Immune Microenvironment-Related Biomarker Promoting the Progression of Papillary Thyroid Cancer MAPK/ERK and PI3K/AKT Pathways.." Frontiers in cell and developmental biology, vol. 9, 2021, pp. 688370.
PMID
35433709
Abstract
Papillary thyroid cancer (PTC) is the most common malignancy of the endocrine system, with an increase in incidence frequency. Major vault protein () is the main structural protein of the vault complex that has already been investigated in specific cancers. Yet the underlying biological functions and molecular mechanisms of in PTC still remain considerably uncharacterized. Comprehensive analyses are predicated on several public datasets and local RNA-Seq cohort. Clinically, we found that was upregulated in human PTC than in non-cancerous thyroid tissue and was correlated with vital clinicopathological parameters in PTC patients. expression was associated with , , , and status, and it was correlated with worse progression-free survival in PTC patients. Functionally, enrichment analysis provided new clues for the close relationship between with cancer-related signaling pathways and the immune microenvironment in PTC. In PTC with high expression, we found CD8 T cells, regulatory T cells, and follicular helper T cells have a higher infiltration level. Intriguingly, expression was positively correlated with multiple distinct phases of the anti-cancer immunity cycle. knockdown significantly suppressed cell viability and colony formation, and promoted apoptosis. In addition, downregulated markedly inhibited the migration and invasion potential of PTC cells. The rescue experiments showed that could reverse the level of cell survival and migration. Mechanistically, exerts its oncogenic function in PTC cells through activating PI3K/AKT/mTOR and MAPK/ERK pathways. These results point out that is a reliable biomarker related to the immune microenvironment and provide a basis for elucidating the oncogenic roles of in PTC progression.
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