2010, Número 3
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Rev Hematol Mex 2010; 11 (3)
Marcadores moleculares de los síndromes mieloproliferativos
Navarro VM
Idioma: Español
Referencias bibliográficas: 27
Paginas: 152-155
Archivo PDF: 58.17 Kb.
RESUMEN
Las neoplasias mieloproliferativas son un conjunto de enfermedades caracterizadas por la presencia de re-arreglos genéticos o mutaciones somáticas en los genes que codifican para proteínas o receptores que están en relación con la actividad proteica cinasa en la tirosina, como el BCR/ABL, JAK 2 y RFCDP 1, confiriéndole ventaja proliferativa y superviviencia al clon neoclásico mieloide de cualquiera de sus tipos granulocitico, eritroide o megacatiocitco. La leucemia mieloide crónica se caracterizada por la coexistencia de t(9;22) o cromosoma Filadelfia, cuyo marcador molecular es suficiente para que se inicie esta enfermedad y el cual puede utilizarse para la investigación de enfermedad mínima residual posterior a la terapia con blanco en la proteína quimérica resultante.
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