Abstract
Transforming growth factor-β (TGF-β) is a ubiquitous cytokine playing an essential role in cell proliferation, differentiation, apoptosis, adhesion and invasion, as well as in cellular microenvironment. In malignant diseases, TGF-β signaling features a growth inhibitory effect at an early stage but aggressive oncogenic activity at the advanced malignant state. Here, we update the current understanding of TGF-β signaling in cancer development and progression with a focus on breast cancer. We also review the current approaches of TGF-β signaling-targeted therapeutics for human malignancies.
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Abbreviations
- CAF:
-
Carcinoma-associated fibroblasts
- EMT:
-
Epithelial-mesenchymal transition
- CdGAP:
-
Cdc42 GTPase-activating protein
- MEC:
-
Mammary epithelial cell
- DMR:
-
DNA mismatch repair
- MSC:
-
Mesenchymal stem cell
- PRD:
-
Proline-rich domain
- PTK:
-
Protein tyrosine kinase
- RANKL:
-
Receptor activator of NF-κB ligand
- TGF-β:
-
Transforming growth factor-β
- TβRI:
-
Type I TGF-β receptor
- TβRII:
-
Type II TGF-β receptor
- VEGF:
-
Vascular endothelial growth factor
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Acknowledgment
This work is supported by a project from Hunan Provincial Natural Science Foundation of China (11JJ4068).
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Xuyu Zu and Qinghai Zhang contributed equally to this work.
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Zu, X., Zhang, Q., Cao, R. et al. Transforming growth factor-β signaling in tumor initiation, progression and therapy in breast cancer: an update. Cell Tissue Res 347, 73–84 (2012). https://doi.org/10.1007/s00441-011-1225-3
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DOI: https://doi.org/10.1007/s00441-011-1225-3