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study mda mb 231  (ATCC)


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    ATCC study mda mb 231
    Study Mda Mb 231, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 2046 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 99 stars, based on 2046 article reviews
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    Ligand-dependent induction of RAR-target genes is suppressed by activation of RAS-ERK signaling. ( A ) A HA-tagged dominant negative form of RARα (HA-DN-RARα) was expressed in MCF7 cells by using lentivirus. Cells were treated with DMSO or RA (1 μM) for 24 h prior to the analyses. Total RNA and proteins were analyzed by RT-PCR (left) and immunoblotting (right), respectively. *, p < 0.05 (one-way ANOVA followed by Tukey post hoc analyses) (mean + s.e.m., n = 4). ( B ) KRAS-V12 was expressed in MCF7 cells by using lentivirus. 4 days after infection of lentivirus, cells were treated with DMSO or RA (1 μM) for 24 h. Total RNA and proteins were analyzed by RT-PCR (left) and immunoblotting (right), respectively. *, p < 0.05 (one-way ANOVA followed by Tukey post hoc analyses) (mean + s.e.m., n = 4). ( C ) KRAS-V12 was expressed in <t>MCF10A</t> cells by using lentivirus. 3 days after infection of lentivirus, cells were treated with DMSO or RA (1 μM) for 24 h. The indicated mRNA levels were analyzed by RT-PCR. (left) Morphology of MCF10A cells expressing KRAS-V12 or control cells. Scale bars: 50 μm. *, p < 0.05 (one-way ANOVA followed by Tukey post hoc analyses) (mean + s.e.m., n = 3). Uncropped immunoblot images are shown in .
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    Ligand-dependent induction of RAR-target genes is suppressed by activation of RAS-ERK signaling. ( A ) A HA-tagged dominant negative form of RARα (HA-DN-RARα) was expressed in MCF7 cells by using lentivirus. Cells were treated with DMSO or RA (1 μM) for 24 h prior to the analyses. Total RNA and proteins were analyzed by RT-PCR (left) and immunoblotting (right), respectively. *, p < 0.05 (one-way ANOVA followed by Tukey post hoc analyses) (mean + s.e.m., n = 4). ( B ) KRAS-V12 was expressed in MCF7 cells by using lentivirus. 4 days after infection of lentivirus, cells were treated with DMSO or RA (1 μM) for 24 h. Total RNA and proteins were analyzed by RT-PCR (left) and immunoblotting (right), respectively. *, p < 0.05 (one-way ANOVA followed by Tukey post hoc analyses) (mean + s.e.m., n = 4). ( C ) KRAS-V12 was expressed in <t>MCF10A</t> cells by using lentivirus. 3 days after infection of lentivirus, cells were treated with DMSO or RA (1 μM) for 24 h. The indicated mRNA levels were analyzed by RT-PCR. (left) Morphology of MCF10A cells expressing KRAS-V12 or control cells. Scale bars: 50 μm. *, p < 0.05 (one-way ANOVA followed by Tukey post hoc analyses) (mean + s.e.m., n = 3). Uncropped immunoblot images are shown in .
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    Ligand-dependent induction of RAR-target genes is suppressed by activation of RAS-ERK signaling. ( A ) A HA-tagged dominant negative form of RARα (HA-DN-RARα) was expressed in MCF7 cells by using lentivirus. Cells were treated with DMSO or RA (1 μM) for 24 h prior to the analyses. Total RNA and proteins were analyzed by RT-PCR (left) and immunoblotting (right), respectively. *, p < 0.05 (one-way ANOVA followed by Tukey post hoc analyses) (mean + s.e.m., n = 4). ( B ) KRAS-V12 was expressed in MCF7 cells by using lentivirus. 4 days after infection of lentivirus, cells were treated with DMSO or RA (1 μM) for 24 h. Total RNA and proteins were analyzed by RT-PCR (left) and immunoblotting (right), respectively. *, p < 0.05 (one-way ANOVA followed by Tukey post hoc analyses) (mean + s.e.m., n = 4). ( C ) KRAS-V12 was expressed in MCF10A cells by using lentivirus. 3 days after infection of lentivirus, cells were treated with DMSO or RA (1 μM) for 24 h. The indicated mRNA levels were analyzed by RT-PCR. (left) Morphology of MCF10A cells expressing KRAS-V12 or control cells. Scale bars: 50 μm. *, p < 0.05 (one-way ANOVA followed by Tukey post hoc analyses) (mean + s.e.m., n = 3). Uncropped immunoblot images are shown in .

    Journal: Cancers

    Article Title: ERK MAP Kinase Signaling Regulates RAR Signaling to Confer Retinoid Resistance on Breast Cancer Cells

    doi: 10.3390/cancers14235890

    Figure Lengend Snippet: Ligand-dependent induction of RAR-target genes is suppressed by activation of RAS-ERK signaling. ( A ) A HA-tagged dominant negative form of RARα (HA-DN-RARα) was expressed in MCF7 cells by using lentivirus. Cells were treated with DMSO or RA (1 μM) for 24 h prior to the analyses. Total RNA and proteins were analyzed by RT-PCR (left) and immunoblotting (right), respectively. *, p < 0.05 (one-way ANOVA followed by Tukey post hoc analyses) (mean + s.e.m., n = 4). ( B ) KRAS-V12 was expressed in MCF7 cells by using lentivirus. 4 days after infection of lentivirus, cells were treated with DMSO or RA (1 μM) for 24 h. Total RNA and proteins were analyzed by RT-PCR (left) and immunoblotting (right), respectively. *, p < 0.05 (one-way ANOVA followed by Tukey post hoc analyses) (mean + s.e.m., n = 4). ( C ) KRAS-V12 was expressed in MCF10A cells by using lentivirus. 3 days after infection of lentivirus, cells were treated with DMSO or RA (1 μM) for 24 h. The indicated mRNA levels were analyzed by RT-PCR. (left) Morphology of MCF10A cells expressing KRAS-V12 or control cells. Scale bars: 50 μm. *, p < 0.05 (one-way ANOVA followed by Tukey post hoc analyses) (mean + s.e.m., n = 3). Uncropped immunoblot images are shown in .

    Article Snippet: All cell lines used in this study (MCF-7, MDA-MB-231, MCF10A, and HEK293T) were obtained from American Type Culture Collection.

    Techniques: Activation Assay, Dominant Negative Mutation, Reverse Transcription Polymerase Chain Reaction, Western Blot, Infection, Expressing, Control