2004
DOI: 10.1074/jbc.m404568200
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Differential Activation of Smads in HeLa and SiHa Cells That Differ in Their Response to Transforming Growth Factor-β

Abstract: We assessed the responsiveness of six human cervical cancer cell lines to transforming growth factor (TGF) -

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Cited by 23 publications
(19 citation statements)
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“…Using SMAD2/SMAD3 knock out fibroblast cell-lines, SMAD 2 and 3 independent actions of TGF-β have been reported earlier [36]. In addition, SMAD independent signalling by TGF-β mediated by other pathways like the MAP kinases namely the p38, ERK and the JNK pathways is also reported [18-20,37-40]. Activation of the p38 and the JNK pathways by TGF-β involves a TGF-β activated kinase called TAK1 (reviewed in [41,42]).…”
Section: Discussionmentioning
confidence: 83%
“…Using SMAD2/SMAD3 knock out fibroblast cell-lines, SMAD 2 and 3 independent actions of TGF-β have been reported earlier [36]. In addition, SMAD independent signalling by TGF-β mediated by other pathways like the MAP kinases namely the p38, ERK and the JNK pathways is also reported [18-20,37-40]. Activation of the p38 and the JNK pathways by TGF-β involves a TGF-β activated kinase called TAK1 (reviewed in [41,42]).…”
Section: Discussionmentioning
confidence: 83%
“…To analyze whether this binding is related to Smad-binding activity, we tested a consensus Smad-binding element sequence in competition assays. 34 This sequence efficiently inhibited binding of the labeled probe to nuclear proteins, which strongly suggested that Smads are required nuclear proteins in the extract for binding to the 29-bp Cox2 element. Stimulation of MECs with BMP6 for 4 hours retarded the mobility and enhanced the intensity of the DNAprotein interaction (Figure 5D), suggesting that BMP6 remodels or posttranslationally modifies the protein complex that binds to this element.…”
Section: Transcriptional Activation Of the Cox2 Promoter By Bmp6mentioning
confidence: 99%
“…Western blotting was performed as described before27. Briefly, cell lysates were prepared in RIPA lysis buffer and the bands were resolved by 10% SDS-PAGE, and transferred to nitrocellulose membrane for immunoblot analysis.…”
Section: Methodsmentioning
confidence: 99%