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Molecular mechanisms of MAZ targeting up-regulation of NDUFS3 expression to promote malignant progression in melanoma.
- Source :
-
Communications biology [Commun Biol] 2024 Nov 12; Vol. 7 (1), pp. 1491. Date of Electronic Publication: 2024 Nov 12. - Publication Year :
- 2024
-
Abstract
- Myc-associated Zinc-finger Protein (MAZ) has been implicated in the malignant progression of various tumors. However, its expression and functional relationship of MAZ in melanoma have not been previously investigated. This study confirms elevated expression of MAZ in melanoma, correlating with poor patient prognosis. Furthermore, our findings demonstrate that MAZ enhances melanoma progression by promoting proliferation, migration and invasion. It is worth noting that we found that MAZ can target and regulate the transcription of NADH dehydrogenase [ubiquinone] iron-sulfur protein 3 (NDUFS3), a core subunit of mitochondrial complex I, to enhance mitochondrial metabolism and thus promote malignant progression of melanoma. Predictive modeling indicates that the co-expression of MAZ and NDUFS3 could serve as a potential prognostic marker for melanoma patients.<br />Competing Interests: Competing interests The authors declare no competing interests. Ethics All animal procedures were conducted according to the National Institutes of Health Guide for the Care and Use of Laboratory Animals and were approved by the Animal Care and Use Committee of Kunming Medical University (permit number: K2020-0006).<br /> (© 2024. The Author(s).)
- Subjects :
- Humans
Cell Line, Tumor
NADH Dehydrogenase metabolism
NADH Dehydrogenase genetics
DNA-Binding Proteins metabolism
DNA-Binding Proteins genetics
Transcription Factors metabolism
Transcription Factors genetics
Cell Proliferation
Electron Transport Complex I metabolism
Electron Transport Complex I genetics
Cell Movement
Animals
Male
Female
Prognosis
Mice
Melanoma genetics
Melanoma pathology
Melanoma metabolism
Gene Expression Regulation, Neoplastic
Disease Progression
Up-Regulation
Subjects
Details
- Language :
- English
- ISSN :
- 2399-3642
- Volume :
- 7
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Communications biology
- Publication Type :
- Academic Journal
- Accession number :
- 39532991
- Full Text :
- https://doi.org/10.1038/s42003-024-07209-y