Abstract
In normal or nonmalignant cells, TGF-β inhibits cellular proliferation through activation of the SMAD-dependent canonical signaling pathway. Recent findings demonstrate that the protein TMEPAI1 can block the cytostatic effects of the canonical TGF-β signaling pathway, while activating cellular proliferation through the noncanonical, SMAD-independent TGF-β signaling pathway. As TMEPAI1 shows increased expression in the poor prognosis basal and HER2 intrinsic subtypes of breast cancer, these findings point to a new avenue of targeted therapy with considerable therapeutic potential.
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Cichon, M. A., & Radisky, D. C. (2014). Cutting the brakes and flooring the gas: How TMEPAI turns TGF-β into a tumor promoter. Genes and Cancer, 5(9–10), 303–305. https://doi.org/10.18632/genesandcancer.34
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