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2014, Number 609

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Rev Med Cos Cen 2014; 71 (609)

Diagnóstico molecular y tratamiento de leucemias

Aragón-González M, Aragón-González C
Full text How to cite this article

Language: Spanish
References: 27
Page: 39-45
PDF size: 180.55 Kb.


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ABSTRACT

During the last years, with molecular biology advances, it has been possible the detection of fusion genes that present encoder sequences of transcription factors. This way it has been demonstrated that the BCRABL fusion gene is responsible of mieloproliferation in Cronical Mielicytic Leukemia. In Acute Promielocytic Leukemia it has to do with chromosomical translocations that envolves the Retinoic Acid’s alpha receptor over 17’s chromosome, forming the PML-RARα, a fusion gene that inhibits cellular differentiation and originates lethal proliferation of immature promielicytes of this pathology. Currently there are proof that show several steps involved in the Leukemia initiation, and based on molecular genetic advances there have been identified several pathological mutations. In this review we analyze the leukemias genomical topicality, its treatment from genetical therapy point of view, as well as the reference of a new indirect marker, the Zap 70.


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Rev Med Cos Cen. 2014;71