Cargando…
Somatic p16(INK4a) loss accelerates melanomagenesis
Loss of p16(INK4a)–RB and ARF–p53 tumor suppressor pathways, as well as activation of RAS–RAF signaling, is seen in a majority of human melanomas. Although heterozygous germline mutations of p16(INK4a) are associated with familial melanoma, most melanomas result from somatic genetic events: often p1...
Autores principales: | Monahan, K B, Rozenberg, G I, Krishnamurthy, J, Johnson, S M, Liu, W, Bradford, M K, Horner, J, DePinho, R A, Sharpless, N E |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007178/ https://www.ncbi.nlm.nih.gov/pubmed/20697345 http://dx.doi.org/10.1038/onc.2010.314 |
Ejemplares similares
-
Ral activation promotes melanomagenesis
por: Zipfel, Patty A., et al.
Publicado: (2010) -
Ultraviolet radiation accelerates BRAF-driven melanomagenesis by targeting TP53
por: Viros, Amaya, et al.
Publicado: (2014) -
Review: The Key Factors to Melanomagenesis
por: (Jitian) Mihulecea, Cristina-Raluca, et al.
Publicado: (2023) -
Wnt and Related Signaling Pathways in Melanomagenesis
por: Keller, Jesse J., et al.
Publicado: (2010) -
Chemotherapy and Stem Cell Transplantation Increase p16(INK4a) Expression, a Biomarker of T-cell Aging
por: Wood, William A., et al.
Publicado: (2016)