Gishizky M L
SUGEN, Inc, Redwood City, CA, USA.
Cytokines Mol Ther. 1996 Dec;2(4):251-61.
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.
嵌合的Bcr-Abl致癌基因与慢性粒细胞白血病(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蛋白是一种复杂结构,由与特定生化和生物学功能相关的离散结构域组成。这些结构域通过激活负责Bcr-Abl致癌行为的不同信号转导途径发挥作用。本综述将阐述我们目前对Bcr-Abl诱导的病理生理学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。