LABORATORY RESEARCH Diamond-Lipid Hybrids Enhance Chemotherapeutic Tolerance and Mediate Tumor Regression Self-assembled nanodiamond-lipid hybrid particles (NDLPs) harness the potent interaction between the nanodiamond (ND)-surface and small molecules, while providing a mechanism for cell-targeted imaging and therapy of triple negative breast cancers. Epidermal growth factor receptor-targeted NDLPs are highly biocompatible particles that provide cell-specific imaging, promote tumor retention of ND-complexes, prevent epirubicin toxicities and mediate regression of triple negative breast cancers. [Adv Mater] Abstract | Press Release Investigation of SSEA-4 Binding Protein in Breast Cancer Cells Researchers report the identification of an SSEA-4-binding protein in a breast cancer cell line, MCF-7. By using affinity capture and glycan microarray techniques, the intracellular FK-506 binding protein 4 (FKBP4) was identified to bind directly to SSEA-4. The biological significance of SSEA-4/FKBP4 interaction was investigated. [J Am Chem Soc] Abstract Rac-Specific Guanine Nucleotide Exchange Factor DOCK1 Is a Critical Regulator of HER2-Mediated Breast Cancer Metastasis Researchers aimed to identify Rac activators that could promote metastasis downstream of human epithelial growth factor receptor 2 (HER2). They investigated if Dedicator of Cytokinesis 1 (DOCK1), based on its evolutionarily conserved role in receptor tyrosine kinases-mediated Rac activation and cell invasion, could be a regulator of metastasis. They report that high expression of DOCK1 in HER2+ and basal breast cancer subtypes inversely correlates with human patients’ survival. [Proc Natl Acad Sci USA] Abstract | Press Release p130Cas Alters the Differentiation Potential of Mammary Luminal Progenitors by Deregulating C-Kit Activity Investigators described that the adaptor protein p130Cas is a crucial regulator of mouse mammary epithelial cell differentiation. [Stem Cells] Abstract Treatment of Triple-Negative Breast Cancer Using Anti-EGFR Directed Radioimmunotherapy Combined with Radiosensitizing Chemotherapy and PARP Inhibitor Scientists used epidermal growth factor receptor (EGFR) as a target for radioimmunotherapy and hypothesized that EGFR-directed radioimmunotherapy can deliver a continuous lethal radiation dose to residual tumors that are radiosensitized by poly(adenosine diphosphate ribose) polymerase (PARP) inhibitors and chemotherapy. [J Nucl Med] Abstract | Press Release Oncostatin-M Promotes Phenotypic Changes Associated with Mesenchymal and Stem Cell-Like Differentiation in Breast Cancer Stimuli that induce epithelial-to-mesenchymal transition (EMT) and cancer stem cell-like features (‘stemness’) are poorly defined. Researchers aimed to determine whether oncostatin-M is a cell-extrinsic driver of EMT and/or stemness. [Oncogene] Abstract CLINICAL RESEARCH Short-Term Outcomes of Screening Mammography Using Computer-Aided Detection: A Population-Based Study of Medicare Enrollees Researchers aimed to determine associations between computer-aided detection use during screening mammography and the incidence of ductal carcinoma in situ and invasive breast cancer, invasive cancer stage, and diagnostic testing. [Ann Intern Med] Abstract | Press Release Cullin1 Is a Novel Marker of Poor Prognosis and a Potential Therapeutic Target in Human Breast Cancer To investigate the role of Cullin1 (Cul1) in the development of breast cancer, researchers examined the expression of Cul1 in breast cancer tissues and analyzed the correlation between Cul1 expression and clinicopathologic variables and patients survival. [Ann Oncol] Abstract Lymphatic and Angiogenic Candidate Genes Predict the Development of Secondary Lymphedema following Breast Cancer Surgery The authors evaluated differences in phenotypic and genotypic characteristics in women who did and did not develop lymphedema following breast cancer treatment. [PLoS One] Full Article | Press Release Functional and Structural Analysis of C-Terminal BRCA1 Missense Variants Researchers aimed to functionally assess a set of 7 missense variants of uncertain significance (Q1409L, S1473P, E1586G, R1589H, Y1703S, W1718L and G1770V) located in the C-terminal region of BRCA1 by combining in silico prediction tools and structural analysis with a transcription activation assay. Structural analysis of the three variants located in the BRCT domains (Y1703S, W1718L and G1770V) reveals significant alterations of BRCT structure. Results suggest that variants Y1703S, W1718L and G1770V can be classified as likely pathogenic BRCA1 mutations. [PLoS One] Full Article | Press Release |