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e0771 mouse breast cancer cell line  (ATCC)


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    Structured Review

    ATCC e0771 mouse breast cancer cell line
    BM‐MSC‐derived myofibroblasts or CAFs were not detected in distal tissue fibrosis or tumors. A) Confocal imaging of kidney sections from normal and UUO‐induced renal fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. B) Confocal imaging of lung sections from normal and bleomycin‐induced pulmonary fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. C) Confocal imaging of liver sections from normal and CCl 4 ‐induced liver fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. D) Confocal imaging of liver sections from normal and DDC‐induced liver fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. E–H) Quantification of the percentages of DAPI + Col1 + myofibroblasts that were ZsGreen + and tdTomato + in renal fibrosis (E), pulmonary fibrosis (F), CCl 4 ‐induced liver fibrosis (G) and DDC‐induced liver fibrosis (H). n = 5 mice from 4 independent experiments. I) Confocal imaging of <t>E0771‐induced</t> subcutaneous tumors from Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Cancer associated fibroblasts (CAFs) were indicated with anti‐Col1 antibody staining. J) Confocal imaging of normal colons and AOM/DSS‐induced colorectal cancer from Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. CAFs were indicated with anti‐Col1 antibody staining. K,L) Quantification of the percentages of DAPI + Col1 + CAFs that were ZsGreen + and tdTomato + in subcutaneous tumors (K) and colorectal cancer (L). n = 3 mice from 3 independent experiments.
    E0771 Mouse Breast Cancer Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 222 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/e0771 mouse breast cancer cell line/product/ATCC
    Average 98 stars, based on 222 article reviews
    e0771 mouse breast cancer cell line - by Bioz Stars, 2026-02
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    Images

    1) Product Images from "Mapping the Tissue‐of‐Origins of Mesenchymal Stromal Cells in Injury Repair"

    Article Title: Mapping the Tissue‐of‐Origins of Mesenchymal Stromal Cells in Injury Repair

    Journal: Advanced Science

    doi: 10.1002/advs.202509533

    BM‐MSC‐derived myofibroblasts or CAFs were not detected in distal tissue fibrosis or tumors. A) Confocal imaging of kidney sections from normal and UUO‐induced renal fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. B) Confocal imaging of lung sections from normal and bleomycin‐induced pulmonary fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. C) Confocal imaging of liver sections from normal and CCl 4 ‐induced liver fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. D) Confocal imaging of liver sections from normal and DDC‐induced liver fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. E–H) Quantification of the percentages of DAPI + Col1 + myofibroblasts that were ZsGreen + and tdTomato + in renal fibrosis (E), pulmonary fibrosis (F), CCl 4 ‐induced liver fibrosis (G) and DDC‐induced liver fibrosis (H). n = 5 mice from 4 independent experiments. I) Confocal imaging of E0771‐induced subcutaneous tumors from Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Cancer associated fibroblasts (CAFs) were indicated with anti‐Col1 antibody staining. J) Confocal imaging of normal colons and AOM/DSS‐induced colorectal cancer from Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. CAFs were indicated with anti‐Col1 antibody staining. K,L) Quantification of the percentages of DAPI + Col1 + CAFs that were ZsGreen + and tdTomato + in subcutaneous tumors (K) and colorectal cancer (L). n = 3 mice from 3 independent experiments.
    Figure Legend Snippet: BM‐MSC‐derived myofibroblasts or CAFs were not detected in distal tissue fibrosis or tumors. A) Confocal imaging of kidney sections from normal and UUO‐induced renal fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. B) Confocal imaging of lung sections from normal and bleomycin‐induced pulmonary fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. C) Confocal imaging of liver sections from normal and CCl 4 ‐induced liver fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. D) Confocal imaging of liver sections from normal and DDC‐induced liver fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. E–H) Quantification of the percentages of DAPI + Col1 + myofibroblasts that were ZsGreen + and tdTomato + in renal fibrosis (E), pulmonary fibrosis (F), CCl 4 ‐induced liver fibrosis (G) and DDC‐induced liver fibrosis (H). n = 5 mice from 4 independent experiments. I) Confocal imaging of E0771‐induced subcutaneous tumors from Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Cancer associated fibroblasts (CAFs) were indicated with anti‐Col1 antibody staining. J) Confocal imaging of normal colons and AOM/DSS‐induced colorectal cancer from Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. CAFs were indicated with anti‐Col1 antibody staining. K,L) Quantification of the percentages of DAPI + Col1 + CAFs that were ZsGreen + and tdTomato + in subcutaneous tumors (K) and colorectal cancer (L). n = 3 mice from 3 independent experiments.

    Techniques Used: Derivative Assay, Imaging, Staining



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    ATCC e0771 mouse breast cancer cell line
    BM‐MSC‐derived myofibroblasts or CAFs were not detected in distal tissue fibrosis or tumors. A) Confocal imaging of kidney sections from normal and UUO‐induced renal fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. B) Confocal imaging of lung sections from normal and bleomycin‐induced pulmonary fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. C) Confocal imaging of liver sections from normal and CCl 4 ‐induced liver fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. D) Confocal imaging of liver sections from normal and DDC‐induced liver fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. E–H) Quantification of the percentages of DAPI + Col1 + myofibroblasts that were ZsGreen + and tdTomato + in renal fibrosis (E), pulmonary fibrosis (F), CCl 4 ‐induced liver fibrosis (G) and DDC‐induced liver fibrosis (H). n = 5 mice from 4 independent experiments. I) Confocal imaging of <t>E0771‐induced</t> subcutaneous tumors from Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Cancer associated fibroblasts (CAFs) were indicated with anti‐Col1 antibody staining. J) Confocal imaging of normal colons and AOM/DSS‐induced colorectal cancer from Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. CAFs were indicated with anti‐Col1 antibody staining. K,L) Quantification of the percentages of DAPI + Col1 + CAFs that were ZsGreen + and tdTomato + in subcutaneous tumors (K) and colorectal cancer (L). n = 3 mice from 3 independent experiments.
    E0771 Mouse Breast Cancer Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC cell lines mouse breast cancer cell eo771 atcc
    BM‐MSC‐derived myofibroblasts or CAFs were not detected in distal tissue fibrosis or tumors. A) Confocal imaging of kidney sections from normal and UUO‐induced renal fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. B) Confocal imaging of lung sections from normal and bleomycin‐induced pulmonary fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. C) Confocal imaging of liver sections from normal and CCl 4 ‐induced liver fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. D) Confocal imaging of liver sections from normal and DDC‐induced liver fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. E–H) Quantification of the percentages of DAPI + Col1 + myofibroblasts that were ZsGreen + and tdTomato + in renal fibrosis (E), pulmonary fibrosis (F), CCl 4 ‐induced liver fibrosis (G) and DDC‐induced liver fibrosis (H). n = 5 mice from 4 independent experiments. I) Confocal imaging of <t>E0771‐induced</t> subcutaneous tumors from Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Cancer associated fibroblasts (CAFs) were indicated with anti‐Col1 antibody staining. J) Confocal imaging of normal colons and AOM/DSS‐induced colorectal cancer from Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. CAFs were indicated with anti‐Col1 antibody staining. K,L) Quantification of the percentages of DAPI + Col1 + CAFs that were ZsGreen + and tdTomato + in subcutaneous tumors (K) and colorectal cancer (L). n = 3 mice from 3 independent experiments.
    Cell Lines Mouse Breast Cancer Cell Eo771 Atcc, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC mouse breast cancer cell lines eo771
    Silence of Hsp47 in adipose tissue suppresses HFD-induced mammary tumor growth. ( A - B ) Tumor growth curve of <t>EO771</t> xenografts in mammary glands of control and Hsp47 Adi-KO mice under HFD (A) conditions ( n = 9). ( C ) Tumor growth curve of Wnt xenografts in mammary glands of control and Hsp47 Adi-KO mice under HFD condition ( n = 4). ( D - F ) IHC staining and quantification of cell proliferation marker Ki67 and cell apoptosis marker active-Caspase3 in tumor tissue from EO771 xenograft models in control and Hsp47 Adi-KO mice under HFD condition ( n = 6). ( G - H ) SHG imaging and quantification of collagen fiber in tumor tissues from EO771 xenograft models in control and Hsp47 Adi-KO mice under HFD condition ( n = 4). ( I ) Administration of Col003 attenuated HFD-induced weight gain in mice ( n = 5). ( J ) Tumors and tumor growth curve of mouse EO771 orthotopic xenograft models in control and Col003 treated mice (HFD) ( n = 10).( K-M ) Quantification of cell proliferation marker Ki67, active-Caspase3, and collagen deposition in EO771 tumors in control and Col003 treated mice (HFD) ( n = 6).Results are presented as mean ± SEM; * p < 0.05; ** p < 0.01; independent Student’s t test. Scar bar: 100 μm
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    ATCC mouse breast cancer cell line eo771
    Silence of Hsp47 in adipose tissue suppresses HFD-induced mammary tumor growth. ( A - B ) Tumor growth curve of <t>EO771</t> xenografts in mammary glands of control and Hsp47 Adi-KO mice under HFD (A) conditions ( n = 9). ( C ) Tumor growth curve of Wnt xenografts in mammary glands of control and Hsp47 Adi-KO mice under HFD condition ( n = 4). ( D - F ) IHC staining and quantification of cell proliferation marker Ki67 and cell apoptosis marker active-Caspase3 in tumor tissue from EO771 xenograft models in control and Hsp47 Adi-KO mice under HFD condition ( n = 6). ( G - H ) SHG imaging and quantification of collagen fiber in tumor tissues from EO771 xenograft models in control and Hsp47 Adi-KO mice under HFD condition ( n = 4). ( I ) Administration of Col003 attenuated HFD-induced weight gain in mice ( n = 5). ( J ) Tumors and tumor growth curve of mouse EO771 orthotopic xenograft models in control and Col003 treated mice (HFD) ( n = 10).( K-M ) Quantification of cell proliferation marker Ki67, active-Caspase3, and collagen deposition in EO771 tumors in control and Col003 treated mice (HFD) ( n = 6).Results are presented as mean ± SEM; * p < 0.05; ** p < 0.01; independent Student’s t test. Scar bar: 100 μm
    Mouse Breast Cancer Cell Line Eo771, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse breast cancer cell line eo771/product/ATCC
    Average 98 stars, based on 1 article reviews
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    CH3 Biosystems mouse eo771 breast cancer cell line
    Silence of Hsp47 in adipose tissue suppresses HFD-induced mammary tumor growth. ( A - B ) Tumor growth curve of <t>EO771</t> xenografts in mammary glands of control and Hsp47 Adi-KO mice under HFD (A) conditions ( n = 9). ( C ) Tumor growth curve of Wnt xenografts in mammary glands of control and Hsp47 Adi-KO mice under HFD condition ( n = 4). ( D - F ) IHC staining and quantification of cell proliferation marker Ki67 and cell apoptosis marker active-Caspase3 in tumor tissue from EO771 xenograft models in control and Hsp47 Adi-KO mice under HFD condition ( n = 6). ( G - H ) SHG imaging and quantification of collagen fiber in tumor tissues from EO771 xenograft models in control and Hsp47 Adi-KO mice under HFD condition ( n = 4). ( I ) Administration of Col003 attenuated HFD-induced weight gain in mice ( n = 5). ( J ) Tumors and tumor growth curve of mouse EO771 orthotopic xenograft models in control and Col003 treated mice (HFD) ( n = 10).( K-M ) Quantification of cell proliferation marker Ki67, active-Caspase3, and collagen deposition in EO771 tumors in control and Col003 treated mice (HFD) ( n = 6).Results are presented as mean ± SEM; * p < 0.05; ** p < 0.01; independent Student’s t test. Scar bar: 100 μm
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    Image Search Results


    BM‐MSC‐derived myofibroblasts or CAFs were not detected in distal tissue fibrosis or tumors. A) Confocal imaging of kidney sections from normal and UUO‐induced renal fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. B) Confocal imaging of lung sections from normal and bleomycin‐induced pulmonary fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. C) Confocal imaging of liver sections from normal and CCl 4 ‐induced liver fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. D) Confocal imaging of liver sections from normal and DDC‐induced liver fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. E–H) Quantification of the percentages of DAPI + Col1 + myofibroblasts that were ZsGreen + and tdTomato + in renal fibrosis (E), pulmonary fibrosis (F), CCl 4 ‐induced liver fibrosis (G) and DDC‐induced liver fibrosis (H). n = 5 mice from 4 independent experiments. I) Confocal imaging of E0771‐induced subcutaneous tumors from Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Cancer associated fibroblasts (CAFs) were indicated with anti‐Col1 antibody staining. J) Confocal imaging of normal colons and AOM/DSS‐induced colorectal cancer from Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. CAFs were indicated with anti‐Col1 antibody staining. K,L) Quantification of the percentages of DAPI + Col1 + CAFs that were ZsGreen + and tdTomato + in subcutaneous tumors (K) and colorectal cancer (L). n = 3 mice from 3 independent experiments.

    Journal: Advanced Science

    Article Title: Mapping the Tissue‐of‐Origins of Mesenchymal Stromal Cells in Injury Repair

    doi: 10.1002/advs.202509533

    Figure Lengend Snippet: BM‐MSC‐derived myofibroblasts or CAFs were not detected in distal tissue fibrosis or tumors. A) Confocal imaging of kidney sections from normal and UUO‐induced renal fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. B) Confocal imaging of lung sections from normal and bleomycin‐induced pulmonary fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. C) Confocal imaging of liver sections from normal and CCl 4 ‐induced liver fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. D) Confocal imaging of liver sections from normal and DDC‐induced liver fibrotic Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Myofibroblasts were indicated with anti‐Col1 antibody staining. E–H) Quantification of the percentages of DAPI + Col1 + myofibroblasts that were ZsGreen + and tdTomato + in renal fibrosis (E), pulmonary fibrosis (F), CCl 4 ‐induced liver fibrosis (G) and DDC‐induced liver fibrosis (H). n = 5 mice from 4 independent experiments. I) Confocal imaging of E0771‐induced subcutaneous tumors from Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. Cancer associated fibroblasts (CAFs) were indicated with anti‐Col1 antibody staining. J) Confocal imaging of normal colons and AOM/DSS‐induced colorectal cancer from Pdgfra creER ;Sp7 dre ;R26 ZT1 mice treated with tamoxifen at 2 months old. CAFs were indicated with anti‐Col1 antibody staining. K,L) Quantification of the percentages of DAPI + Col1 + CAFs that were ZsGreen + and tdTomato + in subcutaneous tumors (K) and colorectal cancer (L). n = 3 mice from 3 independent experiments.

    Article Snippet: The E0771 mouse breast cancer cell line (CRL‐3461, RRID:CVCL_GR23) was obtained from the American Tissue Type Collection (ATCC) in 2018.

    Techniques: Derivative Assay, Imaging, Staining

    Silence of Hsp47 in adipose tissue suppresses HFD-induced mammary tumor growth. ( A - B ) Tumor growth curve of EO771 xenografts in mammary glands of control and Hsp47 Adi-KO mice under HFD (A) conditions ( n = 9). ( C ) Tumor growth curve of Wnt xenografts in mammary glands of control and Hsp47 Adi-KO mice under HFD condition ( n = 4). ( D - F ) IHC staining and quantification of cell proliferation marker Ki67 and cell apoptosis marker active-Caspase3 in tumor tissue from EO771 xenograft models in control and Hsp47 Adi-KO mice under HFD condition ( n = 6). ( G - H ) SHG imaging and quantification of collagen fiber in tumor tissues from EO771 xenograft models in control and Hsp47 Adi-KO mice under HFD condition ( n = 4). ( I ) Administration of Col003 attenuated HFD-induced weight gain in mice ( n = 5). ( J ) Tumors and tumor growth curve of mouse EO771 orthotopic xenograft models in control and Col003 treated mice (HFD) ( n = 10).( K-M ) Quantification of cell proliferation marker Ki67, active-Caspase3, and collagen deposition in EO771 tumors in control and Col003 treated mice (HFD) ( n = 6).Results are presented as mean ± SEM; * p < 0.05; ** p < 0.01; independent Student’s t test. Scar bar: 100 μm

    Journal: Breast Cancer Research : BCR

    Article Title: Hsp47 drives obesity-associated breast cancer progression by enhancing asporin deposition in adipose tissue

    doi: 10.1186/s13058-025-02076-9

    Figure Lengend Snippet: Silence of Hsp47 in adipose tissue suppresses HFD-induced mammary tumor growth. ( A - B ) Tumor growth curve of EO771 xenografts in mammary glands of control and Hsp47 Adi-KO mice under HFD (A) conditions ( n = 9). ( C ) Tumor growth curve of Wnt xenografts in mammary glands of control and Hsp47 Adi-KO mice under HFD condition ( n = 4). ( D - F ) IHC staining and quantification of cell proliferation marker Ki67 and cell apoptosis marker active-Caspase3 in tumor tissue from EO771 xenograft models in control and Hsp47 Adi-KO mice under HFD condition ( n = 6). ( G - H ) SHG imaging and quantification of collagen fiber in tumor tissues from EO771 xenograft models in control and Hsp47 Adi-KO mice under HFD condition ( n = 4). ( I ) Administration of Col003 attenuated HFD-induced weight gain in mice ( n = 5). ( J ) Tumors and tumor growth curve of mouse EO771 orthotopic xenograft models in control and Col003 treated mice (HFD) ( n = 10).( K-M ) Quantification of cell proliferation marker Ki67, active-Caspase3, and collagen deposition in EO771 tumors in control and Col003 treated mice (HFD) ( n = 6).Results are presented as mean ± SEM; * p < 0.05; ** p < 0.01; independent Student’s t test. Scar bar: 100 μm

    Article Snippet: Mouse breast cancer cell lines EO771 was obtained from ATCC.

    Techniques: Control, Immunohistochemistry, Marker, Imaging

    Asporin mediates Hsp47 function in regulating obesity and obesity-associated tumor progression. ( A ) Kaplan-Meier survival analysis showing the association of asporin expression with tumor recurrence in basal-like breast cancer. ASPN: asporin( B ) The body weight growth curve of wide type and asporin KO mice (HFD) (WT group, n = 7; KO group, n = 8). ( C ) Tumor growth curve of mouse EO771 orthotopic xenograft models in control and asporin KO mice (HFD) ( n = 11). ( D - F ) IHC staining and quantification of cell proliferation marker Ki67, and active-Caspase3 inEO771 tumor tissue from control and asporin KO mice under HFD condition ( n = 6). ( G ) Masson’s Trichome staining images and quantification of collagen deposition in E0771 tumor tissues from control and asporin KO mice under HFD condition ( n = 3)( H ) The IVIS images showing treatment of asporin protein promoted breast cancer cell growth in the decellularized mammary gland from Hsp47 Adi-KO mice ( n = 3).Results are presented as mean ± SEM; * p < 0.05; ** p < 0.01; independent Student’s t test. Scar bar: 100 μm

    Journal: Breast Cancer Research : BCR

    Article Title: Hsp47 drives obesity-associated breast cancer progression by enhancing asporin deposition in adipose tissue

    doi: 10.1186/s13058-025-02076-9

    Figure Lengend Snippet: Asporin mediates Hsp47 function in regulating obesity and obesity-associated tumor progression. ( A ) Kaplan-Meier survival analysis showing the association of asporin expression with tumor recurrence in basal-like breast cancer. ASPN: asporin( B ) The body weight growth curve of wide type and asporin KO mice (HFD) (WT group, n = 7; KO group, n = 8). ( C ) Tumor growth curve of mouse EO771 orthotopic xenograft models in control and asporin KO mice (HFD) ( n = 11). ( D - F ) IHC staining and quantification of cell proliferation marker Ki67, and active-Caspase3 inEO771 tumor tissue from control and asporin KO mice under HFD condition ( n = 6). ( G ) Masson’s Trichome staining images and quantification of collagen deposition in E0771 tumor tissues from control and asporin KO mice under HFD condition ( n = 3)( H ) The IVIS images showing treatment of asporin protein promoted breast cancer cell growth in the decellularized mammary gland from Hsp47 Adi-KO mice ( n = 3).Results are presented as mean ± SEM; * p < 0.05; ** p < 0.01; independent Student’s t test. Scar bar: 100 μm

    Article Snippet: Mouse breast cancer cell lines EO771 was obtained from ATCC.

    Techniques: Expressing, Control, Immunohistochemistry, Marker, Staining