LABORATORY RESEARCH A Basal-Like Breast Cancer-Specific Role for SRF–IL6 in YAP-Induced Cancer Stemness Researchers showed that the serum response factor (SRF)-interleukin (IL)-6 axis is the critical mediator of YAP-induced stemness in mammary epithelial cells and breast cancer. [Nat Commun] Full Article Expression and Function of Phosphodiesterase Type 5 in Human Breast Cancer Cell Lines and Tissues: Implications for Targeted Therapy Researchers found that phosphodiesterase 5 is differentially expressed in each molecular subtype of both breast cancer cell lines and tissues, with higher levels representing a startling feature of HER2-positive and triple-negative breast cancers. [Clin Cancer Res] Abstract Context-Specific Effects of TGF-β/SMAD3 in Cancer Are Modulated by the Epigenome The transforming growth factor beta (TGF-β) signaling pathway exerts opposing effects on cancer cells, acting as either a tumor promoter or a tumor suppressor. The authors showed that these opposing effects are a result of the synergy between SMAD3, a downstream effector of TGF-β signaling, and the distinct epigenomes of breast-tumor-initiating cells. [Cell Rep] Full Article | Graphical Abstract Anti-Breast Tumor Activity of Eclipta Extract In-Vitro and In-Vivo: Novel Evidence of Endoplasmic Reticulum Specific Localization of Hsp60 during Apoptosis Scientists performed bio-guided fractionation of Eclipta alba extract and discovered that particularly the chloroform fraction is selectively inducing cytotoxicity to breast cancer cells over non-tumorigenic breast epithelial cells. [Sci Rep] Full Article Effects of PI3K Inhibitor NVP-BKM120 on Overcoming Drug Resistance and Eliminating Cancer Stem Cells in Human Breast Cancer Cells The tumorigenic properties of three multidrug resistance (MDR) breast cancer cell lines to a selective inhibitor of phosphatidylinositol 3-kinase, NVP-BKM120 (BKM120), were assessed. The authors found that BKM120 showed a significant cytotoxic activity on MDR breast cancer cells both in vitro and in vivo. [Cell Death Dis] Full Article Cytoplasmic Levels of cFLIP Determine a Broad Susceptibility of Breast Cancer Stem/Progenitor-Like Cells to TRAIL The authors found that tumor necrosis factor alpha receptor apoptosis inducing ligand (TRAIL) universally suppressed the clonal expansion of stem/progenitors in all six of the breast cancer cell lines tested, irrespective of their phenotype or overall sensitivity to TRAIL. [Mol Cancer] Full Article 184AA3: A Xenograft Model of ER+ Breast Adenocarcinoma The authors focused on six cell lines derived by minimal mutagenesis from normal human breast cells, and asked if any could generate clinically relevant xenografts, which we then extensively characterized. [Breast Cancer Res Treat] Abstract | Press Release Mutation Screening of 1,237 Cancer Genes across Six Model Cell Lines of Basal-Like Breast Cancer Researchers performed mutational profiling of six basal-like breast cancer cell lines and their matched normal lymphocyte DNA using targeted capture and next-generation sequencing of 1,237 cancer-associated genes, including all exons, UTRs and upstream flanking regions. [PLoS One] Full Article CLINICAL RESEARCH Levonorgestrel Intrauterine System for Endometrial Protection in Women with Breast Cancer on Adjuvant Tamoxifen In tamoxifen users, the levonorgestrel-releasing intrauterine system (LNG-IUS) led to a reduction in the incidence of endometrial polyps over both a 12-month period and over a long-term follow-up period. Also the LNG-IUS led to a reduction in the incidence of endometrial hyperplasia over a long-term follow-up period. [Cochrane Database Syst Rev] Abstract Multicentric Neoadjuvant Pilot Phase II Study of Cetuximab Combined with Docetaxel in Operable Triple Negative Breast Cancer Epithelial growth factor receptor is overexpressed in around 50% of triple negative breast cancer (TNBC) and may play a role in its pathogenesis. The authors performed a multicentric pilot Phase II neoadjuvant trial of cetuximab (anti-EGFR antibody) combined with docetaxel for patients with operable, stage II-III TNBC. [Int J Cancer] Abstract |