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Notch signaling as a therapeutic target for breast cancer treatment?

机译:Notch信号作为乳腺癌治疗的靶点吗?

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摘要

Aberrant Notch signaling can induce mammary gland carcinoma in transgenic mice, and high expressions of Notch receptors and ligands have been linked to poor clinical outcomes in human patients with breast cancer. This suggests that inhibition of Notch signaling may be beneficial for breast cancer treatment. In this review, we critically evaluate the evidence that supports or challenges the hypothesis that inhibition of Notch signaling would be advantageous in breast cancer management. We find that there are many remaining uncertainties that must be addressed experimentally if we are to exploit inhibition of Notch signaling as a treatment approach in breast cancer. Nonetheless, Notch inhibition, in combination with other therapies, is a promising avenue for future management of breast cancer. Furthermore, since aberrant Notch4 activity can induce mammary gland carcinoma in the absence of RBPjκ, a better understanding of the components of RBPjκ-independent oncogenic Notch signaling pathways and their contribution to Notch-induced tumorigenesis would facilitate the deployment of Notch inhibition strategies for effective treatment of breast cancer.
机译:Notch信号异常可以在转基因小鼠中诱发乳腺癌,Notch受体和配体的高表达与人类乳腺癌患者的不良临床结局有关。这表明抑制Notch信号传导可能对乳腺癌治疗有益。在这篇综述中,我们严格地评估了支持或挑战假设的证据,即抑制Notch信号传导将有利于乳腺癌的治疗。我们发现,如果我们要利用抑制Notch信号作为乳腺癌的一种治疗方法,则还必须通过实验解决许多遗留的不确定性。尽管如此,Notch抑制与其他疗法相结合,是未来治疗乳腺癌的有前途的途径。此外,由于Notch4的异常活性可在不存在RBPjκ的情况下诱导乳腺癌,因此,更好地了解不依赖RBPjκ的致癌Notch信号通路的成分及其对Notch诱导的肿瘤发生的作用,将有助于Notch抑制策略的有效部署。乳腺癌。

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