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tgf β smad signaling inhibitor sb431542  (MedChemExpress)


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    Structured Review

    MedChemExpress tgf β smad signaling inhibitor sb431542
    Tgf β Smad Signaling Inhibitor Sb431542, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 97/100, based on 318 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tgf+%CE%B2+smad+inhibitor/SB-431542/pmc13095602-55-1-6
    Average 97 stars, based on 318 article reviews
    tgf β smad signaling inhibitor sb431542 - by Bioz Stars, 2026-09
    97/100 stars

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    other:

    Article Title: Combined effects of nanoplastics and 3-BHA at environmentally relevant concentrations significantly aggravated kidney injury via TGF-β/SMAD signaling pathway in mice.
    Article Snippet: The TGF-β/Smad inhibitor (HCTZ, CAS# HY-B0252) was obtained from MCE (USA) to investigate its role in mitigating kidney damage via the TGF-β/Smad pathway.



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    Primer sequences for RT-qPCR.

    Journal: Frontiers in Oncology

    Article Title: Tricellulin facilitates colorectal cancer metastasis through activation of the TGFβ/SMAD2/3 signalling pathway

    doi: 10.3389/fonc.2025.1562976

    Figure Lengend Snippet: Primer sequences for RT-qPCR.

    Article Snippet: To activate or inhibit the TGFβ1/SMAD pathway, cells were treated with an agonist (TGFβ1, 10 ng/ml) or antagonist (SB525334, 5 μM) (MedChemExpress, USA).

    Techniques: Sequencing

    Tricellulin expressions correlated with TGFB1 and SMAD2/3 in CRC. Representative images of IHC staining demonstrating the expression of tricellulin, TGFβ1, and SMAD2/3 in normal and cancerous colorectal tissues (A) . Results of correlation analysis showing the positive correlation between tricellulin and TGFβ1 (B) and SMAD2/3 (C) in CRC tissues. Scale bar =20 μm. *** P<0.001, ****P<0.0001 .

    Journal: Frontiers in Oncology

    Article Title: Tricellulin facilitates colorectal cancer metastasis through activation of the TGFβ/SMAD2/3 signalling pathway

    doi: 10.3389/fonc.2025.1562976

    Figure Lengend Snippet: Tricellulin expressions correlated with TGFB1 and SMAD2/3 in CRC. Representative images of IHC staining demonstrating the expression of tricellulin, TGFβ1, and SMAD2/3 in normal and cancerous colorectal tissues (A) . Results of correlation analysis showing the positive correlation between tricellulin and TGFβ1 (B) and SMAD2/3 (C) in CRC tissues. Scale bar =20 μm. *** P<0.001, ****P<0.0001 .

    Article Snippet: To activate or inhibit the TGFβ1/SMAD pathway, cells were treated with an agonist (TGFβ1, 10 ng/ml) or antagonist (SB525334, 5 μM) (MedChemExpress, USA).

    Techniques: Immunohistochemistry, Expressing

    Tricellulin regulates TGFβ/SMAD2/3 signaling pathway in CRC cells. Results of RT-qPCR showing the relative expression levels of TGFβ1, SMAD2, and SMAD3 under the indicated conditions (A, B) . Representative images (C) and quantified results (D, E) of Western blot analysis demonstrating the expression and/or activation of TGFβ1, SMAD2/3, p-SMAD2, and p-SMAD3 under the indicated conditions. n=3, * P<0.05, **P <0.01, *** P<0.001, ****P<0.0001 .

    Journal: Frontiers in Oncology

    Article Title: Tricellulin facilitates colorectal cancer metastasis through activation of the TGFβ/SMAD2/3 signalling pathway

    doi: 10.3389/fonc.2025.1562976

    Figure Lengend Snippet: Tricellulin regulates TGFβ/SMAD2/3 signaling pathway in CRC cells. Results of RT-qPCR showing the relative expression levels of TGFβ1, SMAD2, and SMAD3 under the indicated conditions (A, B) . Representative images (C) and quantified results (D, E) of Western blot analysis demonstrating the expression and/or activation of TGFβ1, SMAD2/3, p-SMAD2, and p-SMAD3 under the indicated conditions. n=3, * P<0.05, **P <0.01, *** P<0.001, ****P<0.0001 .

    Article Snippet: To activate or inhibit the TGFβ1/SMAD pathway, cells were treated with an agonist (TGFβ1, 10 ng/ml) or antagonist (SB525334, 5 μM) (MedChemExpress, USA).

    Techniques: Quantitative RT-PCR, Expressing, Western Blot, Activation Assay

    Tricellulin modulates TGFβ/SMAD2/3 signaling in CRC cells. Results of RT-qPCR demonstrate the expression of tricellulin (A) , TGFβ1 (B) , SMAD2 (C) , and SMAD3 (D) in CRC cells with or without tricellulin overexpression and treated with SB525334 or vehicle. Results of RT-qPCR showing the expression of tricellulin (E) , TGFβ1 (F) , SMAD2 (G) , and SMAD3 (H) in CRC cells with or without tricellulin knockdown and treated with TGFβ1 or vehicle. Representative images (I) and quantified results of Western blot analysis demonstrating protein levels of tricellulin (J) , ββ1 (K), total SMAD2/3 (L) , phosphorylated SMAD2 (M) , and phosphorylated SMAD3 (N) in CRC cells with or without tricellulin overexpression and treated with SB525334 or vehicle. Representative images (O) and quantified results of Western blot analysis demonstrating protein levels of tricellulin (P) , TGFβ1 (Q) , total SMAD2/3 (R) , phosphorylated SMAD2 (S) , and phosphorylated SMAD3 (T) in CRC cells with or without tricellulin depletion treated with TGFβ1 or vehicle. n=3, * P<0.05, **P <0.01, *** P<0.001, ****P<0.0001. .

    Journal: Frontiers in Oncology

    Article Title: Tricellulin facilitates colorectal cancer metastasis through activation of the TGFβ/SMAD2/3 signalling pathway

    doi: 10.3389/fonc.2025.1562976

    Figure Lengend Snippet: Tricellulin modulates TGFβ/SMAD2/3 signaling in CRC cells. Results of RT-qPCR demonstrate the expression of tricellulin (A) , TGFβ1 (B) , SMAD2 (C) , and SMAD3 (D) in CRC cells with or without tricellulin overexpression and treated with SB525334 or vehicle. Results of RT-qPCR showing the expression of tricellulin (E) , TGFβ1 (F) , SMAD2 (G) , and SMAD3 (H) in CRC cells with or without tricellulin knockdown and treated with TGFβ1 or vehicle. Representative images (I) and quantified results of Western blot analysis demonstrating protein levels of tricellulin (J) , ββ1 (K), total SMAD2/3 (L) , phosphorylated SMAD2 (M) , and phosphorylated SMAD3 (N) in CRC cells with or without tricellulin overexpression and treated with SB525334 or vehicle. Representative images (O) and quantified results of Western blot analysis demonstrating protein levels of tricellulin (P) , TGFβ1 (Q) , total SMAD2/3 (R) , phosphorylated SMAD2 (S) , and phosphorylated SMAD3 (T) in CRC cells with or without tricellulin depletion treated with TGFβ1 or vehicle. n=3, * P<0.05, **P <0.01, *** P<0.001, ****P<0.0001. .

    Article Snippet: To activate or inhibit the TGFβ1/SMAD pathway, cells were treated with an agonist (TGFβ1, 10 ng/ml) or antagonist (SB525334, 5 μM) (MedChemExpress, USA).

    Techniques: Quantitative RT-PCR, Expressing, Over Expression, Knockdown, Western Blot

    Tricellulin promotes CRC growth in vivo . Images of xenograft tumors from mice inoculated with HCT116 cells under indicated modulations (A-C) . Quantification of final tumor weights from indicated groups (D) . Tumor growth curves showing tumor volumes after cell implantation. Representative images of IHC staining of tricellulin, TGFβ1, SMAD2/3, and Ki67 in xenograft tumors (F) . Quantified expression levels of IHC staining intensity for tricellulin (G) , TGFβ1 (H) , SMAD2/3 (I) , and Ki67 (J) . Scale bar = 20 μm. n=5, * P<0.05, **P <0.01.

    Journal: Frontiers in Oncology

    Article Title: Tricellulin facilitates colorectal cancer metastasis through activation of the TGFβ/SMAD2/3 signalling pathway

    doi: 10.3389/fonc.2025.1562976

    Figure Lengend Snippet: Tricellulin promotes CRC growth in vivo . Images of xenograft tumors from mice inoculated with HCT116 cells under indicated modulations (A-C) . Quantification of final tumor weights from indicated groups (D) . Tumor growth curves showing tumor volumes after cell implantation. Representative images of IHC staining of tricellulin, TGFβ1, SMAD2/3, and Ki67 in xenograft tumors (F) . Quantified expression levels of IHC staining intensity for tricellulin (G) , TGFβ1 (H) , SMAD2/3 (I) , and Ki67 (J) . Scale bar = 20 μm. n=5, * P<0.05, **P <0.01.

    Article Snippet: To activate or inhibit the TGFβ1/SMAD pathway, cells were treated with an agonist (TGFβ1, 10 ng/ml) or antagonist (SB525334, 5 μM) (MedChemExpress, USA).

    Techniques: In Vivo, Immunohistochemistry, Expressing