TY - JOUR
T1 - HER2/Neu- and TAK1-mediated Up-regulation of the Transforming Growth Factor β Inhibitor Smad7 via the ETS Protein ER81
AU - Dowdy, Sean C.
AU - Mariani, Andrea
AU - Janknecht, Ralf
PY - 2003/11/7
Y1 - 2003/11/7
N2 - The cytokine transforming growth factor β (TGF-β) plays an important role in preventing tumor formation by blocking cell cycle progression. Accordingly, many cancers demonstrate mutations in TGF-β signaling components or enhanced expression of inhibitors of the TGF-β pathway such as Smad7. In this report we show that the oncoprotein HER2/Neu is able to collaborate with the ETS transcription factor ER81 to activate Smad7 transcription in breast, endometrial, and ovarian cancer cell lines. ER81 binds to two ETS sites within the Smad7 promoter, and mutation of one of these ETS sites greatly decreases Smad7 induction by HER2/Neu and ER81. Furthermore, we show that Smad7 activation involves the processing of signals from HER2/Neu to ER81 via the ERK mitogen-activated protein kinase pathway. Thus, we have uncovered a novel mechanism by which oncogenic HER2/Neu, in collaboration with ER81, can induce carcinogenesis through Smad7 upregulation. Moreover, we show that TAK1, a TGF-β-activated protein kinase, stimulates ER81 via the p38 mitogen-activated protein kinase pathway and thereby induces the Smad7 promoter. This suggests that attenuation of TGF-β signaling by activating Smad7 transcription may proceed not only through TGF-β receptor-regulated Smad proteins but also through an independent pathway involving ER81 and TAK1.
AB - The cytokine transforming growth factor β (TGF-β) plays an important role in preventing tumor formation by blocking cell cycle progression. Accordingly, many cancers demonstrate mutations in TGF-β signaling components or enhanced expression of inhibitors of the TGF-β pathway such as Smad7. In this report we show that the oncoprotein HER2/Neu is able to collaborate with the ETS transcription factor ER81 to activate Smad7 transcription in breast, endometrial, and ovarian cancer cell lines. ER81 binds to two ETS sites within the Smad7 promoter, and mutation of one of these ETS sites greatly decreases Smad7 induction by HER2/Neu and ER81. Furthermore, we show that Smad7 activation involves the processing of signals from HER2/Neu to ER81 via the ERK mitogen-activated protein kinase pathway. Thus, we have uncovered a novel mechanism by which oncogenic HER2/Neu, in collaboration with ER81, can induce carcinogenesis through Smad7 upregulation. Moreover, we show that TAK1, a TGF-β-activated protein kinase, stimulates ER81 via the p38 mitogen-activated protein kinase pathway and thereby induces the Smad7 promoter. This suggests that attenuation of TGF-β signaling by activating Smad7 transcription may proceed not only through TGF-β receptor-regulated Smad proteins but also through an independent pathway involving ER81 and TAK1.
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U2 - 10.1074/jbc.M307202200
DO - 10.1074/jbc.M307202200
M3 - Article
C2 - 12947087
AN - SCOPUS:0242497921
SN - 0021-9258
VL - 278
SP - 44377
EP - 44384
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 45
ER -