The Notch ligand Jagged1 as a target for anti-tumor therapy

被引:153
作者
Li, Demin [1 ]
Masiero, Massimo [1 ]
Banham, Alison H. [1 ]
Harris, Adrian L. [2 ]
机构
[1] Univ Oxford, Weatherall Inst Mol Med, Nuffield Div Clin Lab Sci, Radcliffe Dept Med, Oxford, England
[2] Univ Oxford, Weatherall Inst Mol Med, Dept Oncol, Canc Res UK Mol Oncol Labs, Oxford, England
关键词
Jagged1; Notch pathway; cancer therapy; cancer stem cells; angiogenesis;
D O I
10.3389/fonc.2014.00254
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The Notch pathway is increasingly attracting attention as a source of therapeutic targets for cancer. Ligand-induced Notch signaling has been implicated in various aspects of cancer biology; as a consequence, pan-Notch inhibitors and therapeutic antibodies targeting one or more of the Notch receptors have been investigated for cancer therapy. Alternatively, Notch ligands provide attractive options for therapy in cancer treatment due to their more restricted expression and better-defined functions, as well as their low rate of mutations in cancer. One of the Notch ligands, Jaggedl (JAG1), is overexpressed in many cancer types, and plays an important role in several aspects of tumor biology. In fact, JAG1-stimulated Notch activation is directly implicated in tumor growth through maintaining cancer stem cell populations, promoting cell survival, inhibiting apoptosis, and driving cell proliferation and metastasis. In addition, JAG1 can indirectly affect cancer by influencing tumor microenvironment components such as tumor vasculature and immune cell infiltration. This article gives an overview of JAG1 and its role in tumor biology, and its potential as a therapeutic target.
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页数:13
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