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PHF6 mutations in T-cell acute lymphoblastic leukemia

Tumor suppressor genes on the X chromosome may skew the gender distribution of specific types of cancer1,2. T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive hematological malignancy with an increased incidence in males3. In this study, we report the identification of inactivating mutatio...

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Detalles Bibliográficos
Autores principales: Van Vlierberghe, Pieter, Palomero, Teresa, Khiabanian, Hossein, Van der Meulen, Joni, Castillo, Mireia, Van Roy, Nadine, De Moerloose, Barbara, Philippé, Jan, González-García, Sara, Toribio, María L, Taghon, Tom, Zuurbier, Linda, Cauwelier, Barbara, Harrison, Christine J, Schwab, Claire, Pisecker, Markus, Strehl, Sabine, Langerak, Anton W, Gecz, Jozef, Sonneveld, Edwin, Pieters, Rob, Paietta, Elisabeth, Rowe, Jacob M, Wiernik, Peter H, Benoit, Yves, Soulier, Jean, Poppe, Bruce, Yao, Xiaopan, Cordon-Cardo, Carlos, Meijerink, Jules, Rabadan, Raul, Speleman, Frank, Ferrando, Adolfo
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847364/
https://www.ncbi.nlm.nih.gov/pubmed/20228800
http://dx.doi.org/10.1038/ng.542
Descripción
Sumario:Tumor suppressor genes on the X chromosome may skew the gender distribution of specific types of cancer1,2. T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive hematological malignancy with an increased incidence in males3. In this study, we report the identification of inactivating mutations and deletions in the X-linked plant homeodomain finger 6 (PHF6) gene in 16% of pediatric and 38% of adult primary T-ALL samples. Notably, PHF6 mutations are almost exclusively found in T-ALL samples from male subjects. Mutational loss of PHF6 is significantly associated with leukemias driven by aberrant expression of the homeobox transcription factor oncogenes TLX1 and TLX3. Overall, these results identify PHF6 as a new X-linked tumor suppressor in T-ALL and point to a strong genetic interaction between PHF6 loss and aberrant expression of TLX transcription factors in the pathogenesis of this disease.