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Updated: Apr 29, 2026

Spatial and Temporal Control of Murine Melanoma Initiation from Mutant Melanocyte Stem Cells
Published on: June 7, 2019
Rad6 is a Potential Early Marker of Melanoma Development
Karli Rosner1, Shreelekha Adsule2, Brittany Haynes3
1Department of Dermatology, Wayne State University, 110, East Warren Avenue, Detroit, MI 48201; Center for Molecular Medicine and Genetics, Wayne State University, 110, East Warren Avenue, Detroit, MI 48201; Karmanos Cancer Institute, Wayne State University, 110, East Warren Avenue, Detroit, MI 48201.
Rad6, an enzyme, is overexpressed in melanoma and linked to higher beta-catenin activity, suggesting its potential as an early melanoma development marker.
Area of Science:
- Oncology
- Molecular Biology
- Dermatology
Background:
- Melanoma is a significant cause of cancer death.
- Wnt/β-catenin pathway activation is implicated in melanoma.
- Rad6, an ubiquitin-conjugating enzyme, affects β-catenin stability.
Purpose of the Study:
- Investigate the role of Rad6 in melanoma.
- Examine the relationship between β-catenin, Rad6, and Mitf-M in melanoma.
- Assess Rad6 expression as a potential biomarker for melanoma development.
Main Methods:
- Analyzed Rad6 and β-catenin expression in melanoma cell lines.
- Studied β-catenin transcriptional targets Rad6 and Mitf-M.
- Examined Rad6, β-catenin, and Melan-A expression in nevi and melanoma tissues using immunofluorescence.
Main Results:
- Rad6 is overexpressed in melanoma cell lines compared to normal melanocytes.
- Rad6 overexpression correlates with high molecular weight β-catenin and increased transcriptional activity.
- Rad6/Melan-A dual positivity is significantly associated with melanoma diagnosis.
- Rad6 expression increases in transformed melanoma regions.
Conclusions:
- Rad6 plays a role in melanoma pathogenesis.
- Rad6 expression may serve as an early indicator of melanoma development.
- Rad6 warrants further investigation as a potential melanoma biomarker.
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