TRIM58 downregulation maintains stemness via MYH9-GRK3-YAP axis activation in triple-negative breast cancer stem cells.
TRIM58 is a member of the TRIM protein family, which possess with E3 ubiquitin ligase activities. Studies have revealed that low expression of TRIM58 plays key roles, has been implicated in the tumor progression of tumor formation due to its reduced expression. However, its role in regulating the stemness of ... breast cancer stem cells (CSCs) remains unexplored. Here, we found that TRIM58 was underexpressed in TNBC tissues and cells compared to adjacent mucosa tissue, and its downregulation was significantly associated with shorter survival. Overexpression of TRIM58 reduced the proportion of CD44?+?/CD24- cells, upregulated differentiation genes, and inhibited stemness-related gene expression in TNBC CSCs. In vitro and in vivo experiments revealed that TRIM58 overexpression in CSCs suppressed tumor sphere formation and tumorigenic capacity. Co-IP results indicated direct interaction between TRIM58 and MYH9, with TRIM58 inducing MYH9 degradation via ubiquitination in differentiated cells. Label-free quantitative proteomics identified GRK3 and Hippo-YAP as downstream targets and signaling pathways of MYH9. TIMER database analysis, immunohistochemistry, western blotting, DNA-protein pulldown experiments, and dual luciferase reporter assays demonstrated that MYH9 regulated GRK3 transcriptional activation in CSCs. In conclusion, elevated TRIM58 expression in CSCs downregulates MYH9 protein levels by promoting ubiquitin-mediated degradation, thereby inhibiting downstream GRK3 transcription, inactivating the YAP stemness pathway, and ultimately promoting CSC differentiation.
Mesh Terms:
Adaptor Proteins, Signal Transducing, Animals, Cell Line, Tumor, Down-Regulation, Female, Gene Expression Regulation, Neoplastic, Humans, Mice, Myosin Heavy Chains, Neoplastic Stem Cells, Signal Transduction, Transcription Factors, Tripartite Motif Proteins, Triple Negative Breast Neoplasms, Ubiquitin-Protein Ligases, YAP-Signaling Proteins
Adaptor Proteins, Signal Transducing, Animals, Cell Line, Tumor, Down-Regulation, Female, Gene Expression Regulation, Neoplastic, Humans, Mice, Myosin Heavy Chains, Neoplastic Stem Cells, Signal Transduction, Transcription Factors, Tripartite Motif Proteins, Triple Negative Breast Neoplasms, Ubiquitin-Protein Ligases, YAP-Signaling Proteins
Cancer Gene Ther
Date: Aug. 01, 2024
PubMed ID: 38714850
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