Promyelocytic leukemia-retinoic acid receptorαfusion gene:research advances / 国际药学研究杂志
Journal of International Pharmaceutical Research
; (6): 275-279, 2014.
Artigo
em Chinês
| WPRIM (Pacífico Ocidental)
| ID: wpr-452222
Biblioteca responsável:
WPRO
ABSTRACT
Acute promyelocytic leukemia (APL) is a distinctive subtype of acute myeloid leukemia with a distinct biology and clinical presentation. Its molecular biology characteristic is a aberrant chromosomal translocation of the promyelocytic leukemia (PML) gene on chromosome 15 and the retinoic acid receptor α(RARα) gene on chromosome 17. This translocation generates PML-RARα fusion protein, which plays an important role in the genesis, development, diagnosis and therapy of APL. The PML protein has a close relationship with PML-RARαfusion gene. This article mainly summarizes the character, the function of PML protein and the degradation pathway of PML-RARα.
Texto completo:
Disponível
Base de dados:
WPRIM (Pacífico Ocidental)
Idioma:
Chinês
Revista:
Journal of International Pharmaceutical Research
Ano de publicação:
2014
Tipo de documento:
Artigo