Abstract
Transforming growth factor—β (TGF—β) plays an important physiologic role in the regulation of cell proliferation, motility, and apoptosis as well as extracellular matrix (ECM) production. It therefore modulates physiologic functions such as embryonic development, wound healing, vasculogenesis and angiogenesis, as well as immune surveillance. Moreover, TGF—β has been associated with a wide variety of diseases: atherosclerosis; fibrotic diseases of the lung, kidney, and liver; Alzheimer disease; developmental defects; hereditary hemorrhagic teleangiectasia; as well as both solid tumors and hematologic malignancies. Importantly, TGF—β signaling pathways mediate both early-stage tumor- suppressing, as well as late-stage tumor-promoting, effects. In addition, TGF—β can synergize with oncogenes in transformation and tumor progression. Recent therapeutic approaches in cancer target TGF—β signaling, either alone or in combination with conventional or novel targeted therapy, to improve patient outcome.
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Podar, K., Raje, N., Anderson, K.C. (2007). Inhibition of the TGF-β Signaling Pathway in Tumor Cells. In: Groner, B. (eds) Targeted Interference with Signal Transduction Events. Resent Results in Cancer Research, vol 172. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-31209-3_6
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