Microenvironment Modulated Metastatic CD133+/CXCR4+/EpCAM− Lung Cancer Initiating Cells Sustain Tumor Dissemination and Correlate with Poor Prognosis Investigators showed that CD133+/CXCR4+ cancer initiating cells directly isolated from patient-derived xenografts of non-small cell lung cancer are endowed with superior ability to seed and initiate metastasis at distant organs. [Cancer Res] Abstract | Full Article Pyrvinium Targets CD133 in Human Glioblastoma Brain Tumor-Initiating Cells Using gain/loss-of-function studies for CD133, researchers assessed the in vitro self-renewal and in vivo tumor formation capabilities of patient-derived glioblastoma cells. [Clin Cancer Res] Abstract Dysregulated Protease Activated Receptor 1 (PAR1) Promotes Metastatic Phenotype in Breast Cancer through HMGA2 PAR1 expression increased spheroid formation and the level of stemness markers and self-renewal capacity in human breast cancer cells. They also identified HMGA2 (high mobility group A2) as an important regulator of PAR1-mediated invasion. [Oncogene] Abstract Drug Transporter-Mediated Protection of Cancer Stem Cells from Ionophore Antibiotics Researchers applied chemosensitivity testing of well-characterized human cancer cell lines to elaborate on whether drug transporters are involved in protection from the cytotoxic effects of the ionophore antibiotics salinomycin and nigericin. They demonstrated that ionophore antibiotics were ineffective against both stem-like ovarian cancer side population cells and K562/Dox-H1 cells. [Stem Cells Transl Med] Abstract CAR-Engineered NK Cells Targeting Wild-Type EGFR and EGFRvIII Enhance Killing of Glioblastoma and Patient-Derived Glioblastoma Stem Cells The authors explored whether both wild-type EGFR and EGFRvIII can be effectively targeted by chimeric antigen receptor (CAR)-redirected natural killer (NK) cells to treat glioblastoma. [Sci Rep] Full Article The Senescent Microenvironment Promotes the Emergence of Heterogeneous Cancer Stem-Like Cells Researchers showed that post-crisis cells are not able to form tumors unless a senescent microenvironment is provided. They also demonstrated that explanted cells, while displaying differences in cell differentiation markers, are all endowed with enhanced stem cell properties including self-renewal and multilineage differentiation capacity. [Carcinogenesis] Abstract Extracellular Matrix Properties Regulate the Migratory Response of Glioblastoma Stem Cells in 3D Culture Investigators developed a composite matrix of hyaluronan structurally supported by a collagen-oligomer fibril network to simulate the brain-tumor extracellular matrix (ECM) composition. This model was compared with the most commonly used in vitro three-dimensional (3D) culture formats, Matrigel and collagen type-I monomer matrices, to study how the mechanical and compositional properties of the ECM alter the migration characteristics of glioblastoma stem cell neurospheres. [Tissue Eng Part A] Abstract Temozolomide Sensitizes Stem-Like Cells of Glioma Spheres to TRAIL-Induced Apoptosis via Upregulation of Casitas B-Lineage Lymphoma (c-Cbl) Protein Scientists investigated whether the widely used chemotherapeutic agent temozolomide can sensitize glioma stem-like cells (GSCs) from human glioblastoma multiforme (GBM) to TRAIL-induced apoptosis. GSCs were isolated from GBM, and stem cell properties were confirmed by immunocytochemistry and in vivo tumorigenicity. [Tumor Biol] Abstract Optimum 3D Matrix Stiffness for Maintenance of Cancer Stem Cells Is Dependent on Tissue Origin of Cancer Cells Scientists investigated the effect of cancer cells’ tissue origin on the optimum matrix stiffness for cancer stem cell growth and marker expression in a model polyethylene glycol diacrylate hydrogel without the interference of other factors in the microenvironment. [PLoS One] Full Article ROCK Inhibition Facilitates In Vitro Expansion of Glioblastoma Stem-Like Cells Researchers proposed the use of selective Rho-kinase (ROCK) inhibitors, Y-27632 and fasudil, to promote glioblastoma stem cell/brain tumor initiating cell-like cell survival and propagation in vitro. [PLoS One] Full Article |