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| Content Provider | Springer Nature : BioMed Central |
|---|---|
| Author | Bai, Xupeng Liu, Jiarui Zhou, Shujie Wu, Lingzhi Feng, Xiaojie Zhang, Pumin |
| Abstract | Background Triple-negative breast cancer (TNBC) has pronounced stemness that is associated with relapse. N6-methyladenosine (m6A) plays a crucial role in shaping cellular behavior by modulating transcript expression. However, the role of m6A in TNBC stemness, as well as the mechanisms governing its abundance, has yet to be elucidated. Methods We analyzed proteomic and transcriptomic data derived from breast cancer cohorts, with an emphasis on m6A regulators. To unravel the role of m6A in TNBC, we employed RNA sequencing, methylated RNA immunoprecipitation sequencing, RNA immunoprecipitation, chromatin immunoprecipitation, and luciferase reporter assays with mesenchymal stem-like (MSL) TNBC models. The clinical relevance was validated using human tissue microarrays and publicly accessible databases. Results Our findings indicate that the global level of m6A modification in MSL TNBC is downregulated primarily due to the loss of methyltransferase-like 14 (METTL14). The diminished m6A modification is crucial for the maintenance of TNBC stemness, as it increases the expression of yes-associated protein 1 (YAP1) by blocking YTH domain-containing family protein 2 (YTHDF2)-mediated transcript decay, thereby promoting the activation of Hippo-independent YAP1 signaling. YAP1 is essential for sustaining the stemness regulated by METTL14. Furthermore, we demonstrated that the loss of METTL14 expression results from lysine-specific demethylase 1 (LSD1)-mediated removal of histone H3 lysine 4 methylation at the promoter region, which is critical for LSD1-driven stemness in TNBC. Conclusion These findings present an epi-transcriptional mechanism that maintains Hippo-independent YAP1 signaling and plays a role in preserving the undifferentiated state of TNBC, which indicates the potential for targeting the LSD1-METTL14 axis to address TNBC stemness. |
| Related Links | https://jeccr.biomedcentral.com/counter/pdf/10.1186/s13046-024-03225-2.pdf |
| Ending Page | 22 |
| Page Count | 22 |
| Starting Page | 1 |
| File Format | HTM / HTML |
| ISSN | 17569966 |
| DOI | 10.1186/s13046-024-03225-2 |
| Journal | Journal of Experimental & Clinical Cancer Research |
| Issue Number | 1 |
| Volume Number | 43 |
| Language | English |
| Publisher | BioMed Central |
| Publisher Date | 2024-11-20 |
| Access Restriction | Open |
| Subject Keyword | Cancer Research Immunology Apoptosis Oncology TNBC Stemness METTL14 m6A YAP1 LSD1 |
| Content Type | Text |
| Resource Type | Article |
| Subject | Oncology Cancer Research |
| Journal Impact Factor | 11.4/2023 |
| 5-Year Journal Impact Factor | 11.4/2023 |
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