TGF beta(1) represses proliferation of pancreatic carcinoma cells which correlates with Smad4-independent inhibition of ERK activation

Transforming growth factor beta (TGF beta) is a tumor suppressor acting as inhibitor of cell cycle progression of epithelial cells. We show that treat ment of the pancreatic carcinoma cell lines PANC-1 and BxPC-3 with TGF beta (1) inhibits both growth factor-induced activation of the extracellular sig nal-regulated kinase 2 (ERK2) and translocation of the kinase to the nucleu s. TGF beta(1) causes a concentration-dependent reduction of cell prolifera tion in both cell lines, By measuring ERK activation, we can show that TGF beta(1) is able to repress ERK activation induced by mitogenic stimuli such as EGF, This inhibitory effect of TGF beta(1) is not mediated by suppressi on of Ras or c-Raf-1 activation, but mediated by TGF beta(1)-induced activa tion of a serine-threonine phosphatase, as demonstrated by inhibition of ph osphatases by treatment with okadaic acid. Results obtained in the Smad4-de ficient pancreatic carcinoma cell line BxPC-3, demonstrate that TGF beta(1) -induced growth inhibition is mediated by a Smad4-independent prevention of ERK2 activation. In contrast to the effects of TGF beta(1) on epithelial c ells, mesenchymal NIH3T3 fibroblasts exhibit elevated ERK2 activation and i ncreased cell proliferation in response to TGF beta(1) treatment, Smad4-ind ependent phosphatase-mediated inhibition of mitogen-activated ERK2 represen ts a novel effector pathway contributing to suppression of epithelial pancr eatic carcinoma cell proliferation by TGF beta(1), in addition to the well- known Smad-induced tumor suppressor activity of TGF beta.