immunoperoxidase system Search Results


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Human Protein Atlas muc1 expression in normal human breast cell (mcf-10a) and tnbc cell lines (bt-20, mda-mb-231, mda-mb-468, hcc-70)
Signal pathway and mechanism of <t>MUC1-C</t> regulating TNBC Occurrence and progression (Comprehensive arrangement according to the published articles).
Muc1 Expression In Normal Human Breast Cell (Mcf 10a) And Tnbc Cell Lines (Bt 20, Mda Mb 231, Mda Mb 468, Hcc 70), supplied by Human Protein Atlas, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Signal pathway and mechanism of <t>MUC1-C</t> regulating TNBC Occurrence and progression (Comprehensive arrangement according to the published articles).
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Signal pathway and mechanism of <t>MUC1-C</t> regulating TNBC Occurrence and progression (Comprehensive arrangement according to the published articles).
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Signal pathway and mechanism of <t>MUC1-C</t> regulating TNBC Occurrence and progression (Comprehensive arrangement according to the published articles).
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Verlag GmbH immunoperoxidase staining
Signal pathway and mechanism of <t>MUC1-C</t> regulating TNBC Occurrence and progression (Comprehensive arrangement according to the published articles).
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Signal pathway and mechanism of <t>MUC1-C</t> regulating TNBC Occurrence and progression (Comprehensive arrangement according to the published articles).
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Signal pathway and mechanism of <t>MUC1-C</t> regulating TNBC Occurrence and progression (Comprehensive arrangement according to the published articles).
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Distribuidora Bioquimica Asociada SRL anti-mouse and anti-rabbit universal immunoperoxidase polymer histofine-simple stain max po multi
Signal pathway and mechanism of <t>MUC1-C</t> regulating TNBC Occurrence and progression (Comprehensive arrangement according to the published articles).
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List of the Brazilian thirty most cited articles in general surgery, during the period of 1970–2009 years.
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Image Search Results


Signal pathway and mechanism of MUC1-C regulating TNBC Occurrence and progression (Comprehensive arrangement according to the published articles).

Journal: International Journal of Nanomedicine

Article Title: The Therapeutic Effects of MUC1-C shRNA@Fe 3 O 4 Magnetic Nanoparticles in Alternating Magnetic Fields on Triple-Negative Breast Cancer

doi: 10.2147/IJN.S426849

Figure Lengend Snippet: Signal pathway and mechanism of MUC1-C regulating TNBC Occurrence and progression (Comprehensive arrangement according to the published articles).

Article Snippet: Figure 1 MUC1 and its expressions in various types of tumors (from UCSC genome browser on human, the red pentagram indicates breast invasive carcinoma) ( A ), MUC1 protein expression in different tumor cell lines ( B ) and BRCA cell lines ( C ) (based on datasets of Human Protein Atlas), MUC1 expression between BRCA and normal tissue ( ) (based on datasets of The Cancer Genome Atlas), MUC1 expression in normal human breast cell (MCF-10A) and TNBC cell lines (BT-20, MDA-MB-231, MDA-MB-468, HCC-70) ( E ).

Techniques:

Schematic illustration of MUC1-C shRNA@Fe 3 O 4 MNPs construction and the therapeutic mechanism on TNBC. MUC1-C shRNA and Fe 3 O 4 MNPs were self-assembled into MUC1-C shRNA@ Fe 3 O 4 MNPs by electrostatic adsorption. After entering TNBC cells and under the action of AMF, on the one hand, it induces apoptosis and ferroptosis by targeting MUC1-C, on the other hand, it increases the temperature (43 °C) and the Fe 2+ concentration directly kills TNBC cells and stimulates apoptosis and ferroptosis mechanisms.

Journal: International Journal of Nanomedicine

Article Title: The Therapeutic Effects of MUC1-C shRNA@Fe 3 O 4 Magnetic Nanoparticles in Alternating Magnetic Fields on Triple-Negative Breast Cancer

doi: 10.2147/IJN.S426849

Figure Lengend Snippet: Schematic illustration of MUC1-C shRNA@Fe 3 O 4 MNPs construction and the therapeutic mechanism on TNBC. MUC1-C shRNA and Fe 3 O 4 MNPs were self-assembled into MUC1-C shRNA@ Fe 3 O 4 MNPs by electrostatic adsorption. After entering TNBC cells and under the action of AMF, on the one hand, it induces apoptosis and ferroptosis by targeting MUC1-C, on the other hand, it increases the temperature (43 °C) and the Fe 2+ concentration directly kills TNBC cells and stimulates apoptosis and ferroptosis mechanisms.

Article Snippet: Figure 1 MUC1 and its expressions in various types of tumors (from UCSC genome browser on human, the red pentagram indicates breast invasive carcinoma) ( A ), MUC1 protein expression in different tumor cell lines ( B ) and BRCA cell lines ( C ) (based on datasets of Human Protein Atlas), MUC1 expression between BRCA and normal tissue ( ) (based on datasets of The Cancer Genome Atlas), MUC1 expression in normal human breast cell (MCF-10A) and TNBC cell lines (BT-20, MDA-MB-231, MDA-MB-468, HCC-70) ( E ).

Techniques: shRNA, Adsorption, Concentration Assay

MUC1 and its expressions in various types of tumors (from UCSC genome browser on human, the red pentagram indicates breast invasive carcinoma) ( A ), MUC1 protein expression in different tumor cell lines ( B ) and BRCA cell lines ( C ) (based on datasets of Human Protein Atlas), MUC1 expression between BRCA and normal tissue ( D ) (based on datasets of The Cancer Genome Atlas), MUC1 expression in normal human breast cell (MCF-10A) and TNBC cell lines (BT-20, MDA-MB-231, MDA-MB-468, HCC-70) ( E ). IHC results of MUC1 in TNBC tissues, paraneoplastic tissues and normal breast tissues ( F ). Error bars represent means ± SD. **p<0.01, ****p<0.001.

Journal: International Journal of Nanomedicine

Article Title: The Therapeutic Effects of MUC1-C shRNA@Fe 3 O 4 Magnetic Nanoparticles in Alternating Magnetic Fields on Triple-Negative Breast Cancer

doi: 10.2147/IJN.S426849

Figure Lengend Snippet: MUC1 and its expressions in various types of tumors (from UCSC genome browser on human, the red pentagram indicates breast invasive carcinoma) ( A ), MUC1 protein expression in different tumor cell lines ( B ) and BRCA cell lines ( C ) (based on datasets of Human Protein Atlas), MUC1 expression between BRCA and normal tissue ( D ) (based on datasets of The Cancer Genome Atlas), MUC1 expression in normal human breast cell (MCF-10A) and TNBC cell lines (BT-20, MDA-MB-231, MDA-MB-468, HCC-70) ( E ). IHC results of MUC1 in TNBC tissues, paraneoplastic tissues and normal breast tissues ( F ). Error bars represent means ± SD. **p<0.01, ****p<0.001.

Article Snippet: Figure 1 MUC1 and its expressions in various types of tumors (from UCSC genome browser on human, the red pentagram indicates breast invasive carcinoma) ( A ), MUC1 protein expression in different tumor cell lines ( B ) and BRCA cell lines ( C ) (based on datasets of Human Protein Atlas), MUC1 expression between BRCA and normal tissue ( ) (based on datasets of The Cancer Genome Atlas), MUC1 expression in normal human breast cell (MCF-10A) and TNBC cell lines (BT-20, MDA-MB-231, MDA-MB-468, HCC-70) ( E ).

Techniques: Expressing

Silence efficiency of MUC1-C shRNA on TNBC cell line HCC-70. RT-qPCR ( A ) and Western blot detected the silencing efficiency of MUC1-C shRNA ( B and C ). MUC1-C shRNA (3#) plasmid map ( D ) and target sequence (the highlighted yellow section) ( E ). Error bars represent means ± SD. ****p<0.001.

Journal: International Journal of Nanomedicine

Article Title: The Therapeutic Effects of MUC1-C shRNA@Fe 3 O 4 Magnetic Nanoparticles in Alternating Magnetic Fields on Triple-Negative Breast Cancer

doi: 10.2147/IJN.S426849

Figure Lengend Snippet: Silence efficiency of MUC1-C shRNA on TNBC cell line HCC-70. RT-qPCR ( A ) and Western blot detected the silencing efficiency of MUC1-C shRNA ( B and C ). MUC1-C shRNA (3#) plasmid map ( D ) and target sequence (the highlighted yellow section) ( E ). Error bars represent means ± SD. ****p<0.001.

Article Snippet: Figure 1 MUC1 and its expressions in various types of tumors (from UCSC genome browser on human, the red pentagram indicates breast invasive carcinoma) ( A ), MUC1 protein expression in different tumor cell lines ( B ) and BRCA cell lines ( C ) (based on datasets of Human Protein Atlas), MUC1 expression between BRCA and normal tissue ( ) (based on datasets of The Cancer Genome Atlas), MUC1 expression in normal human breast cell (MCF-10A) and TNBC cell lines (BT-20, MDA-MB-231, MDA-MB-468, HCC-70) ( E ).

Techniques: shRNA, Quantitative RT-PCR, Western Blot, Plasmid Preparation, Sequencing

Characterization of MUC1-C shRNA@Fe 3 O 4 MNPs. Appearance ( A ) and TEM image ( D ) of the prepared MUC1-C shRNA@Fe 3 O 4 MNPs. DSL Size distribution of Fe 3 O 4 MNPs ( B and C ) and MUC1-C shRNA@Fe 3 O 4 MNPs ( E and F ). Tyndall effect of MUC1-C shRNA@Fe 3 O 4 MNPs ( G ). Zeta potential of MUC1-C shRNA@Fe 3 O 4 MNPs ( H ). Encapsulation efficiency at different shRNA/MNPs ratios ( I ). TEM elemental mapping analysis of MUC1-C shRNA@Fe 3 O 4 MNPs ( J ). Raman spectrum of MUC1-C shRNA, Fe 3 O 4 MNPs, and MUC1-C shRNA@Fe 3 O 4 MNPs ( K ). Release profiles of Fe 2+ from MUC1-C shRNA@Fe 3 O 4 MNPs at different pH values with or without AMF ( L ). The heating curves of MUC1-C shRNA@Fe 3 O 4 MNPs with different concentrations (50–250μg/mL) ( M ). Hemolysis test at different concentrations (MUC1-C shRNA@Fe 3 O 4 MNPs) (n=3) ( N and O ). Hemolysis test (200μg/mL, n=3) ( P and Q ). Error bars represent means ± SD. TEM scale bar: 50nm.

Journal: International Journal of Nanomedicine

Article Title: The Therapeutic Effects of MUC1-C shRNA@Fe 3 O 4 Magnetic Nanoparticles in Alternating Magnetic Fields on Triple-Negative Breast Cancer

doi: 10.2147/IJN.S426849

Figure Lengend Snippet: Characterization of MUC1-C shRNA@Fe 3 O 4 MNPs. Appearance ( A ) and TEM image ( D ) of the prepared MUC1-C shRNA@Fe 3 O 4 MNPs. DSL Size distribution of Fe 3 O 4 MNPs ( B and C ) and MUC1-C shRNA@Fe 3 O 4 MNPs ( E and F ). Tyndall effect of MUC1-C shRNA@Fe 3 O 4 MNPs ( G ). Zeta potential of MUC1-C shRNA@Fe 3 O 4 MNPs ( H ). Encapsulation efficiency at different shRNA/MNPs ratios ( I ). TEM elemental mapping analysis of MUC1-C shRNA@Fe 3 O 4 MNPs ( J ). Raman spectrum of MUC1-C shRNA, Fe 3 O 4 MNPs, and MUC1-C shRNA@Fe 3 O 4 MNPs ( K ). Release profiles of Fe 2+ from MUC1-C shRNA@Fe 3 O 4 MNPs at different pH values with or without AMF ( L ). The heating curves of MUC1-C shRNA@Fe 3 O 4 MNPs with different concentrations (50–250μg/mL) ( M ). Hemolysis test at different concentrations (MUC1-C shRNA@Fe 3 O 4 MNPs) (n=3) ( N and O ). Hemolysis test (200μg/mL, n=3) ( P and Q ). Error bars represent means ± SD. TEM scale bar: 50nm.

Article Snippet: Figure 1 MUC1 and its expressions in various types of tumors (from UCSC genome browser on human, the red pentagram indicates breast invasive carcinoma) ( A ), MUC1 protein expression in different tumor cell lines ( B ) and BRCA cell lines ( C ) (based on datasets of Human Protein Atlas), MUC1 expression between BRCA and normal tissue ( ) (based on datasets of The Cancer Genome Atlas), MUC1 expression in normal human breast cell (MCF-10A) and TNBC cell lines (BT-20, MDA-MB-231, MDA-MB-468, HCC-70) ( E ).

Techniques: shRNA, Zeta Potential Analyzer, Encapsulation

Cellular uptake of NPs. Cellular uptake of MUC1-C shRNA@Fe 3 O 4 MNPs in the HCC-70 cells was observed under a CLSM. Green fluorescence indicates MUC1-C shRNA@Fe 3 O 4 -FITC and blue fluorescence indicates the nucleus ( A ). Investigation of internalization pathway of MUC1-C shRNA@Fe 3 O 4 MNPs in HCC-70 cells in the presence of different endocytosis inhibitors (n=3) ( B ). Error bars represent means ± SD. Scale bar: 50μm. ****p<0.001.

Journal: International Journal of Nanomedicine

Article Title: The Therapeutic Effects of MUC1-C shRNA@Fe 3 O 4 Magnetic Nanoparticles in Alternating Magnetic Fields on Triple-Negative Breast Cancer

doi: 10.2147/IJN.S426849

Figure Lengend Snippet: Cellular uptake of NPs. Cellular uptake of MUC1-C shRNA@Fe 3 O 4 MNPs in the HCC-70 cells was observed under a CLSM. Green fluorescence indicates MUC1-C shRNA@Fe 3 O 4 -FITC and blue fluorescence indicates the nucleus ( A ). Investigation of internalization pathway of MUC1-C shRNA@Fe 3 O 4 MNPs in HCC-70 cells in the presence of different endocytosis inhibitors (n=3) ( B ). Error bars represent means ± SD. Scale bar: 50μm. ****p<0.001.

Article Snippet: Figure 1 MUC1 and its expressions in various types of tumors (from UCSC genome browser on human, the red pentagram indicates breast invasive carcinoma) ( A ), MUC1 protein expression in different tumor cell lines ( B ) and BRCA cell lines ( C ) (based on datasets of Human Protein Atlas), MUC1 expression between BRCA and normal tissue ( ) (based on datasets of The Cancer Genome Atlas), MUC1 expression in normal human breast cell (MCF-10A) and TNBC cell lines (BT-20, MDA-MB-231, MDA-MB-468, HCC-70) ( E ).

Techniques: shRNA, Fluorescence

MUC1-C shRNA@Fe 3 O 4 MNPs suppress the migration, invasion, and proliferation in HCC-70 cell lines. Wound healing ( A ), Transwell ( B ), CCK-8 OD 450nm ( C ), and inhibition rate based on CCK-8 ( D and E ). The protein bands ( F ) and quantitative statistical results ( G ) of Bax, cleaved-caspase3, GPX4, NRF2, and FTH1 of HCC-70 cell lines (n=3). Error bars represent means ± SD. *p<0.05, **p<0.01, ***p<0.005, ****p<0.001.

Journal: International Journal of Nanomedicine

Article Title: The Therapeutic Effects of MUC1-C shRNA@Fe 3 O 4 Magnetic Nanoparticles in Alternating Magnetic Fields on Triple-Negative Breast Cancer

doi: 10.2147/IJN.S426849

Figure Lengend Snippet: MUC1-C shRNA@Fe 3 O 4 MNPs suppress the migration, invasion, and proliferation in HCC-70 cell lines. Wound healing ( A ), Transwell ( B ), CCK-8 OD 450nm ( C ), and inhibition rate based on CCK-8 ( D and E ). The protein bands ( F ) and quantitative statistical results ( G ) of Bax, cleaved-caspase3, GPX4, NRF2, and FTH1 of HCC-70 cell lines (n=3). Error bars represent means ± SD. *p<0.05, **p<0.01, ***p<0.005, ****p<0.001.

Article Snippet: Figure 1 MUC1 and its expressions in various types of tumors (from UCSC genome browser on human, the red pentagram indicates breast invasive carcinoma) ( A ), MUC1 protein expression in different tumor cell lines ( B ) and BRCA cell lines ( C ) (based on datasets of Human Protein Atlas), MUC1 expression between BRCA and normal tissue ( ) (based on datasets of The Cancer Genome Atlas), MUC1 expression in normal human breast cell (MCF-10A) and TNBC cell lines (BT-20, MDA-MB-231, MDA-MB-468, HCC-70) ( E ).

Techniques: shRNA, Migration, CCK-8 Assay, Inhibition

The in vivo therapeutic effects of the MUC1-C shRNA@Fe 3 O 4 MNPs on TNBC. IR thermal images of TNBC-bearing C-NKG mice with local injection of MUC1-C shRNA@Fe 3 O 4 MNPs (200 µg mL −1 ), or normal saline under AMF (3Kw) ( A ). Images ( B ) and weights ( C ) of xenograft tumors harvested from the mice after various treatments on the 25th day. Tumor volumes ( D ) and Body weight ( E ) growth in mice were measured after different treatments every 5 days within 25 days (n=4). Prussian blue reaction of tumor tissue showing iron staining and tumor necrosis, labeled area was typical necrosis (200x) ( F ). Expression of Bax, cleaved-caspase 3, GPX4, NRF2, and FTH1 in tumor tissues ( G ). Quantitative statistical results according to the protein bands ( H ). Error bars represent means ± SD. *p<0.05, **p<0.01, ***p<0.005, ****p<0.001.

Journal: International Journal of Nanomedicine

Article Title: The Therapeutic Effects of MUC1-C shRNA@Fe 3 O 4 Magnetic Nanoparticles in Alternating Magnetic Fields on Triple-Negative Breast Cancer

doi: 10.2147/IJN.S426849

Figure Lengend Snippet: The in vivo therapeutic effects of the MUC1-C shRNA@Fe 3 O 4 MNPs on TNBC. IR thermal images of TNBC-bearing C-NKG mice with local injection of MUC1-C shRNA@Fe 3 O 4 MNPs (200 µg mL −1 ), or normal saline under AMF (3Kw) ( A ). Images ( B ) and weights ( C ) of xenograft tumors harvested from the mice after various treatments on the 25th day. Tumor volumes ( D ) and Body weight ( E ) growth in mice were measured after different treatments every 5 days within 25 days (n=4). Prussian blue reaction of tumor tissue showing iron staining and tumor necrosis, labeled area was typical necrosis (200x) ( F ). Expression of Bax, cleaved-caspase 3, GPX4, NRF2, and FTH1 in tumor tissues ( G ). Quantitative statistical results according to the protein bands ( H ). Error bars represent means ± SD. *p<0.05, **p<0.01, ***p<0.005, ****p<0.001.

Article Snippet: Figure 1 MUC1 and its expressions in various types of tumors (from UCSC genome browser on human, the red pentagram indicates breast invasive carcinoma) ( A ), MUC1 protein expression in different tumor cell lines ( B ) and BRCA cell lines ( C ) (based on datasets of Human Protein Atlas), MUC1 expression between BRCA and normal tissue ( ) (based on datasets of The Cancer Genome Atlas), MUC1 expression in normal human breast cell (MCF-10A) and TNBC cell lines (BT-20, MDA-MB-231, MDA-MB-468, HCC-70) ( E ).

Techniques: In Vivo, shRNA, Injection, Saline, Staining, Labeling, Expressing

Serum biochemistry indicators assessment of TNBC mice (n=4). Alanine aminotransferase (ALT), Aspartate aminotransferase (AST), Alkaline phosphatase (ALP), Total bilirubin (TBIL). Blood urea nitrogen (BUN), Creatinine (CR) ( A ). Effect of MUC1-C shRNA@Fe 3 O 4 MNPs on the histopathology of heart, lung, spleen, Kidney, and liver from TNBC mice ( B ). Error bars represent means ± SD. Scale bar: 100μm.

Journal: International Journal of Nanomedicine

Article Title: The Therapeutic Effects of MUC1-C shRNA@Fe 3 O 4 Magnetic Nanoparticles in Alternating Magnetic Fields on Triple-Negative Breast Cancer

doi: 10.2147/IJN.S426849

Figure Lengend Snippet: Serum biochemistry indicators assessment of TNBC mice (n=4). Alanine aminotransferase (ALT), Aspartate aminotransferase (AST), Alkaline phosphatase (ALP), Total bilirubin (TBIL). Blood urea nitrogen (BUN), Creatinine (CR) ( A ). Effect of MUC1-C shRNA@Fe 3 O 4 MNPs on the histopathology of heart, lung, spleen, Kidney, and liver from TNBC mice ( B ). Error bars represent means ± SD. Scale bar: 100μm.

Article Snippet: Figure 1 MUC1 and its expressions in various types of tumors (from UCSC genome browser on human, the red pentagram indicates breast invasive carcinoma) ( A ), MUC1 protein expression in different tumor cell lines ( B ) and BRCA cell lines ( C ) (based on datasets of Human Protein Atlas), MUC1 expression between BRCA and normal tissue ( ) (based on datasets of The Cancer Genome Atlas), MUC1 expression in normal human breast cell (MCF-10A) and TNBC cell lines (BT-20, MDA-MB-231, MDA-MB-468, HCC-70) ( E ).

Techniques: shRNA, Histopathology

List of the Brazilian thirty most cited articles in general surgery, during the period of 1970–2009 years.

Journal: Clinics

Article Title: Cited Brazilian papers in general surgery between 1970 and 2009

doi: 10.1590/S1807-59322010000500010

Figure Lengend Snippet: List of the Brazilian thirty most cited articles in general surgery, during the period of 1970–2009 years.

Article Snippet: 1 , 194 , Restaging of colorectal cancer based on the identification of lymph node micrometastases through immunoperoxidase staining of CEA and cytokeratins. , 1991 , Dis Colon Rectum , Cutait R, et al. , USP Hosp Sirio Libanes , Brazil , Cutait R, Alves VA, Lopes LC, Cutait DE, Borges JL, Singer J, da Silva JH, Goffi FS..

Techniques: Immunoperoxidase Staining, Marker, Immunohistochemical staining, Activity Assay, Transplantation Assay, Saline, Dissection, Comparison, Diagnostic Assay, Wilms Tumor Assay, Cell Culture, Irradiation, Modification