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abcb1 inhibitor encequidar  (Topscience Co Ltd)

 
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    Topscience Co Ltd abcb1 inhibitor encequidar
    GRP78 promotes TNBC chemoresistance by regulating ATP binding cassette subfamily B member 1 <t>(ABCB1)-mediated</t> DOX efflux. (A) Fluorescence detection of DOX in Cal51 and Cal51 R cells. (B) Western blotting of GRP78 and fluorescence detection of DOX in GRP78-treated Cal51 R cells treated with DOX (1 μmol/L) in the presence or absence of Encequidar (100 nmol/L). (C) Co-IP assay of GRP78 and ABCB1 in Cal51 R cells. (D) Immunofluorescence staining of GRP78 and ABCB1 in ABCB1-Myc/Cal51 R . (E) Analysis of ABCB1 nanodiscs via electron microscopy. (F) Western blotting of ABCB1 expression in nanodiscs derived from Ctrl/HeLa and ABCB1/HeLa cells. (G) ATPase activity assay of ABCB1 nanodiscs with purified GST or GST-GRP78 proteins. (H–M) Cell viability (H), colony formation (I), cell apoptosis (J, K) and γ H2AX foci formation (L, M) were examined in shGRP78/Cal51 R cells treated with DOX alone or in combination with Encequidar (100 nmol/L). ∗∗∗ P < 0.001; ns represents no significant difference; the data in A, B, I, J and M were assessed via unpaired Student's t -test. The data are presented as the mean ± SD in (A, B, G–J, M). The data are representative of three (A, B, G, I, J, M) or four (H) independent experiments.
    Abcb1 Inhibitor Encequidar, supplied by Topscience Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/abcb1+inhibitor+encequidar/abcb1+inhibitor+encequidar/pmc12144991-51-4-7
    Average 90 stars, based on 1 article reviews
    abcb1 inhibitor encequidar - by Bioz Stars, 2026-10
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    1) Product Images from "USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells"

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells

    Journal: Acta Pharmaceutica Sinica. B

    doi: 10.1016/j.apsb.2025.03.004

    GRP78 promotes TNBC chemoresistance by regulating ATP binding cassette subfamily B member 1 (ABCB1)-mediated DOX efflux. (A) Fluorescence detection of DOX in Cal51 and Cal51 R cells. (B) Western blotting of GRP78 and fluorescence detection of DOX in GRP78-treated Cal51 R cells treated with DOX (1 μmol/L) in the presence or absence of Encequidar (100 nmol/L). (C) Co-IP assay of GRP78 and ABCB1 in Cal51 R cells. (D) Immunofluorescence staining of GRP78 and ABCB1 in ABCB1-Myc/Cal51 R . (E) Analysis of ABCB1 nanodiscs via electron microscopy. (F) Western blotting of ABCB1 expression in nanodiscs derived from Ctrl/HeLa and ABCB1/HeLa cells. (G) ATPase activity assay of ABCB1 nanodiscs with purified GST or GST-GRP78 proteins. (H–M) Cell viability (H), colony formation (I), cell apoptosis (J, K) and γ H2AX foci formation (L, M) were examined in shGRP78/Cal51 R cells treated with DOX alone or in combination with Encequidar (100 nmol/L). ∗∗∗ P < 0.001; ns represents no significant difference; the data in A, B, I, J and M were assessed via unpaired Student's t -test. The data are presented as the mean ± SD in (A, B, G–J, M). The data are representative of three (A, B, G, I, J, M) or four (H) independent experiments.
    Figure Legend Snippet: GRP78 promotes TNBC chemoresistance by regulating ATP binding cassette subfamily B member 1 (ABCB1)-mediated DOX efflux. (A) Fluorescence detection of DOX in Cal51 and Cal51 R cells. (B) Western blotting of GRP78 and fluorescence detection of DOX in GRP78-treated Cal51 R cells treated with DOX (1 μmol/L) in the presence or absence of Encequidar (100 nmol/L). (C) Co-IP assay of GRP78 and ABCB1 in Cal51 R cells. (D) Immunofluorescence staining of GRP78 and ABCB1 in ABCB1-Myc/Cal51 R . (E) Analysis of ABCB1 nanodiscs via electron microscopy. (F) Western blotting of ABCB1 expression in nanodiscs derived from Ctrl/HeLa and ABCB1/HeLa cells. (G) ATPase activity assay of ABCB1 nanodiscs with purified GST or GST-GRP78 proteins. (H–M) Cell viability (H), colony formation (I), cell apoptosis (J, K) and γ H2AX foci formation (L, M) were examined in shGRP78/Cal51 R cells treated with DOX alone or in combination with Encequidar (100 nmol/L). ∗∗∗ P < 0.001; ns represents no significant difference; the data in A, B, I, J and M were assessed via unpaired Student's t -test. The data are presented as the mean ± SD in (A, B, G–J, M). The data are representative of three (A, B, G, I, J, M) or four (H) independent experiments.

    Techniques Used: Binding Assay, Fluorescence, Western Blot, Co-Immunoprecipitation Assay, Immunofluorescence, Staining, Electron Microscopy, Expressing, Derivative Assay, Activity Assay, Purification

    Increased expression of USP51, GRP78 and ABCB1 is correlated with chemoresistance in TNBC. (A) Representative image of immunohistochemical staining of USP51, GRP78 and ABCB1 in serial sections from chemoresistant and nonresistant tumors is shown. (B–D) Direct associations of USP51, GRP78 and ABCB1 expression with chemoresistance were observed in human breast cancer samples. (E) Positive correlation between USP51 and GRP78 expression was observed in human breast cancer samples. (F, G) A positive correlation between the USP51 and GRP78 contents and pathological grade was observed in human breast cancer samples. (H, I) Direct associations between USP51 and GRP78 expression levels and advanced TNM stage were observed in human breast cancer samples. (J–L) Direct associations of USP51, GRP78 and ABCB1 expression with chemoresistance were observed in human TNBC samples. (M) A positive correlation between USP51 expression and GRP78 expression was observed in human TNBC samples. (N, O) A positive association between USP51 and GRP78 expression levels and pathological grade was observed in human TNBC samples. (P, Q) Direct associations between USP51 and GRP78 contents and advanced TNM stage were observed in human TNBC samples. (R–U) Kaplan–Meier curves of overall survival in TNBC patients with high or low expression of USP51, GRP78 and ABCB1 in their breast tumors. The data in B–U were assessed via Spearman's rank correction test.
    Figure Legend Snippet: Increased expression of USP51, GRP78 and ABCB1 is correlated with chemoresistance in TNBC. (A) Representative image of immunohistochemical staining of USP51, GRP78 and ABCB1 in serial sections from chemoresistant and nonresistant tumors is shown. (B–D) Direct associations of USP51, GRP78 and ABCB1 expression with chemoresistance were observed in human breast cancer samples. (E) Positive correlation between USP51 and GRP78 expression was observed in human breast cancer samples. (F, G) A positive correlation between the USP51 and GRP78 contents and pathological grade was observed in human breast cancer samples. (H, I) Direct associations between USP51 and GRP78 expression levels and advanced TNM stage were observed in human breast cancer samples. (J–L) Direct associations of USP51, GRP78 and ABCB1 expression with chemoresistance were observed in human TNBC samples. (M) A positive correlation between USP51 expression and GRP78 expression was observed in human TNBC samples. (N, O) A positive association between USP51 and GRP78 expression levels and pathological grade was observed in human TNBC samples. (P, Q) Direct associations between USP51 and GRP78 contents and advanced TNM stage were observed in human TNBC samples. (R–U) Kaplan–Meier curves of overall survival in TNBC patients with high or low expression of USP51, GRP78 and ABCB1 in their breast tumors. The data in B–U were assessed via Spearman's rank correction test.

    Techniques Used: Expressing, Immunohistochemical staining, Staining

    Working model concerning the mechanism of the USP51/GRP78/ABCB1 network in TNBC chemoresistance.
    Figure Legend Snippet: Working model concerning the mechanism of the USP51/GRP78/ABCB1 network in TNBC chemoresistance.

    Techniques Used:

    Related Articles

    Binding Assay:

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells
    Article Snippet: proteasome inhibitor MG132 (Selleck, TX, USA) was used at a concentration of 20 μmol/L. .. The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Fluorescence:

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells
    Article Snippet: proteasome inhibitor MG132 (Selleck, TX, USA) was used at a concentration of 20 μmol/L. .. The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Western Blot:

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells
    Article Snippet: proteasome inhibitor MG132 (Selleck, TX, USA) was used at a concentration of 20 μmol/L. .. The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Co-Immunoprecipitation Assay:

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells
    Article Snippet: proteasome inhibitor MG132 (Selleck, TX, USA) was used at a concentration of 20 μmol/L. .. The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Immunofluorescence:

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells
    Article Snippet: proteasome inhibitor MG132 (Selleck, TX, USA) was used at a concentration of 20 μmol/L. .. The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Staining:

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells
    Article Snippet: proteasome inhibitor MG132 (Selleck, TX, USA) was used at a concentration of 20 μmol/L. .. The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Electron Microscopy:

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells
    Article Snippet: proteasome inhibitor MG132 (Selleck, TX, USA) was used at a concentration of 20 μmol/L. .. The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Expressing:

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells
    Article Snippet: proteasome inhibitor MG132 (Selleck, TX, USA) was used at a concentration of 20 μmol/L. .. The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Derivative Assay:

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells
    Article Snippet: proteasome inhibitor MG132 (Selleck, TX, USA) was used at a concentration of 20 μmol/L. .. The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Activity Assay:

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells
    Article Snippet: proteasome inhibitor MG132 (Selleck, TX, USA) was used at a concentration of 20 μmol/L. .. The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Purification:

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells
    Article Snippet: proteasome inhibitor MG132 (Selleck, TX, USA) was used at a concentration of 20 μmol/L. .. The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Immunohistochemical staining:

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells
    Article Snippet: proteasome inhibitor MG132 (Selleck, TX, USA) was used at a concentration of 20 μmol/L. .. The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.



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    abcb1 inhibitor encequidar  (Topscience Co Ltd)
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    Topscience Co Ltd abcb1 inhibitor encequidar
    GRP78 promotes TNBC chemoresistance by regulating ATP binding cassette subfamily B member 1 <t>(ABCB1)-mediated</t> DOX efflux. (A) Fluorescence detection of DOX in Cal51 and Cal51 R cells. (B) Western blotting of GRP78 and fluorescence detection of DOX in GRP78-treated Cal51 R cells treated with DOX (1 μmol/L) in the presence or absence of Encequidar (100 nmol/L). (C) Co-IP assay of GRP78 and ABCB1 in Cal51 R cells. (D) Immunofluorescence staining of GRP78 and ABCB1 in ABCB1-Myc/Cal51 R . (E) Analysis of ABCB1 nanodiscs via electron microscopy. (F) Western blotting of ABCB1 expression in nanodiscs derived from Ctrl/HeLa and ABCB1/HeLa cells. (G) ATPase activity assay of ABCB1 nanodiscs with purified GST or GST-GRP78 proteins. (H–M) Cell viability (H), colony formation (I), cell apoptosis (J, K) and γ H2AX foci formation (L, M) were examined in shGRP78/Cal51 R cells treated with DOX alone or in combination with Encequidar (100 nmol/L). ∗∗∗ P < 0.001; ns represents no significant difference; the data in A, B, I, J and M were assessed via unpaired Student's t -test. The data are presented as the mean ± SD in (A, B, G–J, M). The data are representative of three (A, B, G, I, J, M) or four (H) independent experiments.
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    abcb1 inhibitor jo urn al pr e p roo f 5 encequidar  (TargetMol)
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    Figure 7 Increased expression of USP51, GRP78 and <t>ABCB1</t> is correlated with
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    Image Search Results


    GRP78 promotes TNBC chemoresistance by regulating ATP binding cassette subfamily B member 1 (ABCB1)-mediated DOX efflux. (A) Fluorescence detection of DOX in Cal51 and Cal51 R cells. (B) Western blotting of GRP78 and fluorescence detection of DOX in GRP78-treated Cal51 R cells treated with DOX (1 μmol/L) in the presence or absence of Encequidar (100 nmol/L). (C) Co-IP assay of GRP78 and ABCB1 in Cal51 R cells. (D) Immunofluorescence staining of GRP78 and ABCB1 in ABCB1-Myc/Cal51 R . (E) Analysis of ABCB1 nanodiscs via electron microscopy. (F) Western blotting of ABCB1 expression in nanodiscs derived from Ctrl/HeLa and ABCB1/HeLa cells. (G) ATPase activity assay of ABCB1 nanodiscs with purified GST or GST-GRP78 proteins. (H–M) Cell viability (H), colony formation (I), cell apoptosis (J, K) and γ H2AX foci formation (L, M) were examined in shGRP78/Cal51 R cells treated with DOX alone or in combination with Encequidar (100 nmol/L). ∗∗∗ P < 0.001; ns represents no significant difference; the data in A, B, I, J and M were assessed via unpaired Student's t -test. The data are presented as the mean ± SD in (A, B, G–J, M). The data are representative of three (A, B, G, I, J, M) or four (H) independent experiments.

    Journal: Acta Pharmaceutica Sinica. B

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells

    doi: 10.1016/j.apsb.2025.03.004

    Figure Lengend Snippet: GRP78 promotes TNBC chemoresistance by regulating ATP binding cassette subfamily B member 1 (ABCB1)-mediated DOX efflux. (A) Fluorescence detection of DOX in Cal51 and Cal51 R cells. (B) Western blotting of GRP78 and fluorescence detection of DOX in GRP78-treated Cal51 R cells treated with DOX (1 μmol/L) in the presence or absence of Encequidar (100 nmol/L). (C) Co-IP assay of GRP78 and ABCB1 in Cal51 R cells. (D) Immunofluorescence staining of GRP78 and ABCB1 in ABCB1-Myc/Cal51 R . (E) Analysis of ABCB1 nanodiscs via electron microscopy. (F) Western blotting of ABCB1 expression in nanodiscs derived from Ctrl/HeLa and ABCB1/HeLa cells. (G) ATPase activity assay of ABCB1 nanodiscs with purified GST or GST-GRP78 proteins. (H–M) Cell viability (H), colony formation (I), cell apoptosis (J, K) and γ H2AX foci formation (L, M) were examined in shGRP78/Cal51 R cells treated with DOX alone or in combination with Encequidar (100 nmol/L). ∗∗∗ P < 0.001; ns represents no significant difference; the data in A, B, I, J and M were assessed via unpaired Student's t -test. The data are presented as the mean ± SD in (A, B, G–J, M). The data are representative of three (A, B, G, I, J, M) or four (H) independent experiments.

    Article Snippet: The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Techniques: Binding Assay, Fluorescence, Western Blot, Co-Immunoprecipitation Assay, Immunofluorescence, Staining, Electron Microscopy, Expressing, Derivative Assay, Activity Assay, Purification

    Increased expression of USP51, GRP78 and ABCB1 is correlated with chemoresistance in TNBC. (A) Representative image of immunohistochemical staining of USP51, GRP78 and ABCB1 in serial sections from chemoresistant and nonresistant tumors is shown. (B–D) Direct associations of USP51, GRP78 and ABCB1 expression with chemoresistance were observed in human breast cancer samples. (E) Positive correlation between USP51 and GRP78 expression was observed in human breast cancer samples. (F, G) A positive correlation between the USP51 and GRP78 contents and pathological grade was observed in human breast cancer samples. (H, I) Direct associations between USP51 and GRP78 expression levels and advanced TNM stage were observed in human breast cancer samples. (J–L) Direct associations of USP51, GRP78 and ABCB1 expression with chemoresistance were observed in human TNBC samples. (M) A positive correlation between USP51 expression and GRP78 expression was observed in human TNBC samples. (N, O) A positive association between USP51 and GRP78 expression levels and pathological grade was observed in human TNBC samples. (P, Q) Direct associations between USP51 and GRP78 contents and advanced TNM stage were observed in human TNBC samples. (R–U) Kaplan–Meier curves of overall survival in TNBC patients with high or low expression of USP51, GRP78 and ABCB1 in their breast tumors. The data in B–U were assessed via Spearman's rank correction test.

    Journal: Acta Pharmaceutica Sinica. B

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells

    doi: 10.1016/j.apsb.2025.03.004

    Figure Lengend Snippet: Increased expression of USP51, GRP78 and ABCB1 is correlated with chemoresistance in TNBC. (A) Representative image of immunohistochemical staining of USP51, GRP78 and ABCB1 in serial sections from chemoresistant and nonresistant tumors is shown. (B–D) Direct associations of USP51, GRP78 and ABCB1 expression with chemoresistance were observed in human breast cancer samples. (E) Positive correlation between USP51 and GRP78 expression was observed in human breast cancer samples. (F, G) A positive correlation between the USP51 and GRP78 contents and pathological grade was observed in human breast cancer samples. (H, I) Direct associations between USP51 and GRP78 expression levels and advanced TNM stage were observed in human breast cancer samples. (J–L) Direct associations of USP51, GRP78 and ABCB1 expression with chemoresistance were observed in human TNBC samples. (M) A positive correlation between USP51 expression and GRP78 expression was observed in human TNBC samples. (N, O) A positive association between USP51 and GRP78 expression levels and pathological grade was observed in human TNBC samples. (P, Q) Direct associations between USP51 and GRP78 contents and advanced TNM stage were observed in human TNBC samples. (R–U) Kaplan–Meier curves of overall survival in TNBC patients with high or low expression of USP51, GRP78 and ABCB1 in their breast tumors. The data in B–U were assessed via Spearman's rank correction test.

    Article Snippet: The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Techniques: Expressing, Immunohistochemical staining, Staining

    Working model concerning the mechanism of the USP51/GRP78/ABCB1 network in TNBC chemoresistance.

    Journal: Acta Pharmaceutica Sinica. B

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells

    doi: 10.1016/j.apsb.2025.03.004

    Figure Lengend Snippet: Working model concerning the mechanism of the USP51/GRP78/ABCB1 network in TNBC chemoresistance.

    Article Snippet: The dose of the ABCB1 inhibitor Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Techniques:

    Figure 7 Increased expression of USP51, GRP78 and ABCB1 is correlated with

    Journal: Acta Pharmaceutica Sinica B

    Article Title: USP51/GRP78/ABCB1 axis confers chemoresistance through decreasing doxorubicin accumulation in triple-negative breast cancer cells

    doi: 10.1016/j.apsb.2025.03.004

    Figure Lengend Snippet: Figure 7 Increased expression of USP51, GRP78 and ABCB1 is correlated with

    Article Snippet: The dose of the ABCB1 inhibitor Jo urn al Pr e-p roo f 5 Encequidar (TOPSCIENCE, Shanghai, China) was 100 nmol/L.

    Techniques: Expressing