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- W4362014997 abstract "<p>Figure S1 Quantification of Western blot analysis (related to Figure 1) (A-H). Data are presented as mean fold increases ({plus minus}SD) in treated groups over basal values from three independent experiments. *p < 0.01 versus controls; #p < 0.01 versus their corresponding DMSO controls. FFA facilitates TGF-beta-induced ERK activation and SAMD4 nuclear retention, Related to Figure 1. I, Nuclear extracts were made from MDA-MB-231 cells that were treated with 3 ng/ml of TGF-beta for the time points shown. They were analyzed by Western blotting with antibodies against Smad4 or phosphor-ERK and ERK. H3 was used as a loading control for nuclear fractions. We evaluated the cytoplasmic contamination of the nuclear fractions by blotting for α-vinculin. J, Nuclear extracts were made from MDA-MB-231 cells treated with 3 ng/ml of TGF-beta in the presence of palmitate (PA, 400 microM) for the time points shown. Phosphor-ERK and ERK and nuclear SMAD4 were analyzed by Western blotting.</p>" @default.
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- W4362014997 date "2023-03-31" @default.
- W4362014997 modified "2023-10-18" @default.
- W4362014997 title "Supplemental Fig 1 from Aberrant Phosphorylation of SMAD4 Thr277-Mediated USP9x–SMAD4 Interaction by Free Fatty Acids Promotes Breast Cancer Metastasis" @default.
- W4362014997 doi "https://doi.org/10.1158/0008-5472.22418034" @default.
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