Molecular mechanisms of Bcr-Abl-induced oncogenesis.

Cytokines and molecular therapy Pub Date : 1996-12-01
M L Gishizky
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引用次数: 0

Abstract

The chimeric Bcr-Abl oncogene has been implicated in the pathogenesis of chronic myelogenous leukemia (CML) and Philadelphia chromosome (Ph1)-positive acute lymphocytic leukemia (ALL). The Bcr-Abl protein is a complex structure comprising discrete domains associated with specific biochemical and biological functions. These domains function through their ability to activate distinct signal transduction pathways responsible for Bcr-Abl's oncogenic behavior. This review will present our current understanding of signal transduction pathways involved in Bcr-Abl-induced pathophysiology, with particular emphasis on potential targets for therapeutic intervention.

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bcr - abl诱导肿瘤发生的分子机制。
嵌合的Bcr-Abl癌基因与慢性髓性白血病(CML)和费城染色体(Ph1)阳性急性淋巴细胞白血病(ALL)的发病机制有关。Bcr-Abl蛋白是一个复杂的结构,包含与特定生化和生物学功能相关的离散结构域。这些结构域通过激活与Bcr-Abl的致癌行为相关的不同信号转导途径发挥作用。这篇综述将介绍我们目前对bcr - abl诱导的病理生理中涉及的信号转导途径的理解,特别强调治疗干预的潜在靶点。
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