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Notch信号通路在乳腺癌与肿瘤血管生成中的作用:相互作用及治疗潜力

Notch signaling in breast cancer and tumor angiogenesis: cross-talk and therapeutic potentials.

作者信息

Shi Wen, Harris Adrian L

机构信息

Molecular Oncology Laboratories, Cancer Research UK, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Headington, Oxford OX3 9DS, UK.

出版信息

J Mammary Gland Biol Neoplasia. 2006 Jan;11(1):41-52. doi: 10.1007/s10911-006-9011-7.

Abstract

Notch signaling is an evolutionarily conserved pathway that regulates numerous physiological processes. Disruption of Notch has been implicated in multiple tumor types. Evidence from in vitro experiments, mouse models and human tumor samples indicates that Notch plays a predominantly oncogenic role in breast cancer and interacts with other pathways involved in tumorigenesis. In addition, Notch signaling is required for physiological angiogenesis and may promote tumor angiogenesis. A variety of strategies for blocking Notch signaling, in particular gamma-secretase inhibition, are discussed as potential therapies for breast cancer and tumor angiogenesis.

摘要

Notch信号通路是一条在进化上保守的通路,可调节众多生理过程。Notch的破坏与多种肿瘤类型有关。体外实验、小鼠模型和人类肿瘤样本的证据表明,Notch在乳腺癌中主要发挥致癌作用,并与其他参与肿瘤发生的通路相互作用。此外,Notch信号通路是生理性血管生成所必需的,可能促进肿瘤血管生成。作为乳腺癌和肿瘤血管生成的潜在治疗方法,讨论了多种阻断Notch信号通路的策略,特别是γ-分泌酶抑制。

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