LABORATORY RESEARCH A SUMOylation-Dependent Transcriptional Subprogram Is Required for Myc-Driven Tumorigenesis To identify pathways supporting the Myc oncogenic program, scientists used a genome-wide RNAi screen to search for Myc-synthetic lethal genes and uncovered a role for the SUMO-activating enzyme. [Science] Abstract | Press Release Upregulation of miR-1245 by c-Myc Targets BRCA2 and Impairs DNA Repair In this study, researchers demonstrated that miR-1245 directly suppressed BRCA2 3’-UTR and translation, impaired homologous recombination-mediated repair, reduced DNA damage-induced Rad51 nuclear foci and rendered cells hypersensitive to γ-irradiation, ultimately inducing high chromosomal abnormalities in normal breast cells and breast cancer cells. [J Mol Cell Biol] Abstract Immune Recognition of Tumor-Associated Mucin MUC1 Is Achieved by a Fully Synthetic Aberrantly Glycosylated MUC1 Tripartite Vaccine Investigators have identified the minimum requirements to consistently induce cytotoxic T lymphocytes and antibody-dependent cell-mediated cytotoxicity-mediating antibodies specific for the tumor form of MUC1 resulting in a therapeutic response in a mouse model of mammary cancer. [Proc Natl Acad Sci USA] Abstract | Press Release S100A7 Enhances Mammary Tumorigenesis through Upregulation of Inflammatory Pathways Here, scientists report the consequences of psoriasin (S100A7)’s expression on inflammatory pathways that impact breast cancer growth. [Cancer Res] Abstract A Pharmacological Inhibitor of the Protease Taspase1 Effectively Inhibits Breast and Brain Tumor Growth In this study, researchers developed and evaluated small molecule inhibitors of Taspase1 as a new candidate class of therapeutic modalities. [Cancer Res] Abstract Proyl Isomerase Pin1 Facilitates Ubiquitin-Mediated Degradation of Cyclin-Dependent Kinase 10 to Induce Tamoxifen Resistance in Breast Cancer Cells The aim of this study was to elucidate the mechanisms by which downregulation of CDK10 expression confers resistance to tamoxifen in breast cancer. [Oncogene] Abstract MicroRNA-520/373 Family Functions as a Tumor Suppressor in Estrogen Receptor Negative Breast Cancer by Targeting NF-κB and Transforming Growth Factor-β Signaling Pathways Here, investigators performed an unbiased whole genome microRNA (miRNA) screen to identify novel modulators of nuclear factor κB (NF-κB) pathway in breast cancer. [Oncogene] Abstract Opposing Effects of Runx2 and Estradiol on Breast Cancer Cell Proliferation: In Vitro Identification of Reciprocally-Regulated Gene Signature Related to Clinical Letrozole Responsiveness The purpose of this study is to assess the clinical significance of the interaction between estrogen and Runx2 signaling, previously demonstrated in vitro. [Clin Cancer Res] Abstract Regulation of Sodium Iodide Symporter Gene Expression by the Rac1/p38β MAP Kinase Signaling Pathway in MCF-7 Breast Cancer Cells To identify a signal transduction pathway that selectively stimulates sodium/iodide symporter gene expression, scientists investigated regulation by the Rac1-p38 signaling pathway in MCF-7 breast cancer cells and compared it with regulation in FRTL-5 rat thyroid cells. [J Biol Chem] Abstract Matrix Compliance and RhoA Direct the Differentiation of Mammary Progenitor Cells Here, investigators examined how the mechanical properties of the microenvironment affect the differentiation of mammary progenitor cells. [Biomech Model Mechanobiol] Abstract CLINICAL RESEARCH Prognostic Effect of Circulating Adiponectin in a Randomized 2 × 2 Trial of Low-Dose Tamoxifen and Fenretinide in Premenopausal Women at Risk for Breast Cancer Scientists investigated the associations of plasma leptin and adiponectin with mammographic density and disease status and assessed their prognostic effect on recurrence-free survival in premenopausal women at risk for breast cancer. [J Clin Oncol] Abstract Intravenous or Oral Vinorelbine Plus Capecitabine as First-Line Treatment in HER2-Metastatic Breast Cancer: Joint Analysis of 2 Consecutive Prospective Phase II Trials The purpose of this study was to assess the activity and safety of the combination of vinorelbine and capecitabine as first-line treatment in HER2-negative metastatic breast cancer. [Clin Breast Cancer] Abstract  |