Mammary Cell News Volume 13.13 | Apr 8 2021

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    2021-04-08 | MCN 13.13


    Mammary Cell News by STEMCELL Technologies
    Vol. 13.13 – 8 April, 2021
    TOP STORY

    Epigenetic Remodeling Hydrogel Patches for Multidrug‐Resistant Triple‐Negative Breast Cancer

    A tumor‐microenvironment‐responsive hydrogel patch was designed to modulate the plasticity of tumor‐initiating cells in TNBC, which was insensitive to hormone‐ and HER2‐targeting.
    [Advanced Materials]

    Abstract

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    PUBLICATIONSRanked by the impact factor of the journal

    Metabolic Modulation by CDK4/6 Inhibitor Promotes Chemokine-Mediated Recruitment of T Cells Into Mammary Tumors

    Investigators showed that cyclin-dependent kinases 4 and 6 (CDK4/6i) could enhance the efficacy of T cell-based therapies, such as adoptive T cell transfer or T cell-activating antibodies anti-OX40/anti-4-1BB, in murine breast cancer models.
    [Cell Reports]

    Full ArticleGraphical Abstract

    CCL8 Mediates Crosstalk between Endothelial Colony Forming Cells and Triple-Negative Breast Cancer Cells through IL-8, Aggravating Invasion and Tumorigenicity

    Using an indirect co-culture system, scientists showed that co-culture increased the invasive and migratory phenotypes of both MDA-MB-231 TNBC cells and endothelial colony-forming cells.
    [Oncogene]

    Abstract

    Proton Pump Inhibitors Suppress DNA Damage Repair and Sensitize Treatment Resistance in Breast Cancer by Targeting Fatty Acid Synthase

    Researchers showed that the FDA-approved proton pump inhibitors effectively inhibited fatty acid synthase and suppressed breast cancer cell survival.
    [Cancer Letters]

    Abstract

    MCPIP1-Mediated NFIC Alternative Splicing Inhibits Proliferation of Triple-Negative Breast Cancer via Cyclin D1-RB-E2F1 Axis

    Investigators showed that monocyte chemotactic protein induced protein 1 (MCPIP1) was downregulated in 80 TNBC tissues and five TNBC cell lines compared to adjacent paracancerous tissues and one human immortalized breast epithelial cell line, while its high expression levels were associated with increased overall survival in TNBC patients.
    [Cell Death & Disease]

    Full Article

    Association between the Nucleosome Footprint of Plasma DNA and Neoadjuvant Chemotherapy Response for Breast Cancer

    Scientists carried out the nucleosome positioning on cfDNA from 85 breast cancer patients and 85 healthy individuals and two cancer cell lines T-47D and MDA-MB-231 using low-coverage whole-genome sequencing
    [npj Breast Cancer]

    Full Article

    Targeting Nucleotide Metabolism Enhances the Efficacy of Anthracyclines and Anti-Metabolites in Triple-Negative Breast Cancer

    Deoxyuridine 5′-triphosphate nucleotidohydrolase inhibition significantly sensitized TNBC cell lines to fluoropyrimidines and anthracyclines through imbalanced nucleotide pools and increased DNA damage leading to decreased proliferation and increased cell death.
    [npj Breast Cancer]

    Full Article

    The Modulation of PD-L1 Induced by the Oncogenic HBXIP for Breast Cancer Growth

    The mechanisms of controlling programmed death ligand-1 (PD-L1) at the transcription and protein acetylation levels in promoting breast cancer growth are presented. Overexpressed PD-L1 accelerated breast cancer growth in vitro and in vivo.
    [Acta Pharmacologica Sinica]

    Abstract

    KDM3B-ETF1 Fusion Gene Downregulates LMO2 via the WNT/β-Catenin Signaling Pathway, Promoting Metastasis of Invasive Ductal Carcinoma

    Researchers investigated the possible effects KDM3B-ETF1 fusion gene had on breast cancer cell metastasis, invasion and its downstream signaling mediators as revealed from RNA sequence data analysis.
    [Cancer Gene Therapy]

    Abstract

    Nectin-4 and p95-ErbB2 Cooperatively Regulate Hippo Signaling-Dependent SOX2 Gene Expression, Enhancing Anchorage-Independent T47D Cell Proliferation

    The authors found that nectin-4 and p95-ErbB2, but not nectin-4 and either ErbB2 or ErbB2∆Ex16, cooperatively enhanced SOX2 gene expression and cell proliferation in a suspension culture.
    [Scientific Reports]

    Full Article

    MiR-485 Targets the DTX4 Gene to Regulate Milk Fat Synthesis in Bovine Mammary Epithelial Cells

    The relationship between the candidate target gene DTX4 and miR-485 was validated by bioinformatics and real-time fluorescent quantitative PCR and Western blot analyses in bovine mammary epithelial cells.
    [Scientific Reports]

    Full Article

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    REVIEWS

    Breast Cancer as an Example of Tumor Heterogeneity and Tumor Cell Plasticity during Malignant Progression

    Investigators used breast cancer as an example of the origins of tumor heterogeneity and of tumor cell plasticity, as well as considering interclonal cooperativity and cell plasticity as sources of cancer cell heterogeneity.
    [British Journal of Cancer]

    Full Article

    INDUSTRY AND POLICY NEWS

    FDA Approves Trodelvy® the First Treatment for Metastatic Triple-Negative Breast Cancer Shown to Improve Progression-Free Survival and Overall Survival

    Gilead Sciences, Inc. announced that the FDA has granted full approval to Trodelvy® for adult patients with unresectable locally advanced or metastatic TNBC who have received two or more prior systemic therapies, at least one of them for metastatic disease.
    [Gilead Sciences, Inc.]

    Press Release

    FEATURED EVENT

    EMBO Workshop: Cancer Immunometabolism

    November 29 – December 1, 2021
    Barcelona, Spain

    > See All Events

    JOB OPPORTUNITIES

    Postdoctoral Fellow – Breast Cancer Research

    North Carolina Central University – Kannapolis, North Carolina, United States

    Postdoctoral Fellowship – Breast Cancer Immunology and Immunotherapy

    The University of Texas Southwestern Medical Center – Dallas, Texas, United States

    Postdoctoral Position – Translational Breast Cancer Research

    UT Southwestern Medical Center – Dallas, Texas, United States

    Medicinal Chemist – Muscle-Wasting, Neurodegeneration, and Oncology

    Almac – Belfast, Ireland

    Postdoctoral Fellowship – Cancer Molecular Genetics and Therapeutics

    Mass General Cancer Center – Boston, Massachusetts, United States

    > See All Jobs

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