A peptide encoded by LINC00944 suppresses the growth of melanoma cells by diminishing EP400-MYC interaction
[Display omitted] The peptides encoded by long noncoding RNAs (lncRNAs) have been shown to participate in cancer pathogenesis. In this study, lncRNA LINC00944 was validated to encode an endogenous 102-amino acid (aa) small peptide (named LINC00944 peptide). Functionally, LINC00944 peptide exerted an...
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Veröffentlicht in: | Biochemical pharmacology 2024-11, Vol.231, p.116652, Article 116652 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | [Display omitted]
The peptides encoded by long noncoding RNAs (lncRNAs) have been shown to participate in cancer pathogenesis. In this study, lncRNA LINC00944 was validated to encode an endogenous 102-amino acid (aa) small peptide (named LINC00944 peptide). Functionally, LINC00944 peptide exerted an anti-growth effect in melanoma cells in vitro. Mechanistically, LINC00944 peptide interacted with the E1A binding protein p400 (EP400)/c-MYC complex. LINC00944 peptide also inhibited c-MYC protein expression. Furthermore, LINC00944 peptide repressed the transcriptional activity of MYC by reducing the EP400-MYC interaction, thereby reducing the levels of fatty acid metabolism- and glucose metabolism-related proteins. Our findings uncovered that LINC00944 peptide might be a promising adjuvant therapeutic agent for melanoma.
Implications: This study provided the first evidence that LINC00944-encoded peptide played a critical role in the growth of melanoma cells. |
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ISSN: | 0006-2952 1873-2968 1873-2968 |
DOI: | 10.1016/j.bcp.2024.116652 |