Tag results:
epithelial cells
Mammary Cell News
Single-Cell Transcriptomics Reveal the Heterogeneity and Dynamic of Cancer Stem-Like Cells during Breast Tumor Progression
[Cell Death & Disease] The authors used the breast cancer mouse model MMTV-PyMT, and constructed a single-cell atlas of 31,778 cells from four distinct stages of tumor progression, during which malignant transition occured.
Mammary Cell News
Dual Recombinase Action in the Normal and Neoplastic Mammary Gland Epithelium
[Scientific Reports] Researchers demonstrated the versatile applicability of the new MMTV-Flp strain and manipulated genes in a temporally and spatially controlled manner in the normal mammary gland, in luminal-type mammary tumors that overexpressed ERBB2, and in a new KRAS-associated mammary cancer model.
Intestinal Cell News
Strategies for Genetic Manipulation of Adult Stem Cell-Derived Organoids
[Experimental & Molecular Medicine] Scientists focus on adult gastrointestinal organoids and summarize the state-of-the-art protocols for successful transgenesis.
Pulmonary Cell News
Gene Transfer of MRCKα Rescues Lipopolysaccharide-Induced Acute Lung Injury by Restoring Alveolar Capillary Barrier Function
[Scientific Reports] Researchers investigated whether electroporation-mediated gene transfer of MRCKα to the lungs can attenuate LPS-induced acute lung injury in vivo.
Immune Regulation News
The Membrane-Linked Adaptor FRS2β Fashions a Cytokine-Rich Inflammatory Microenvironment That Promotes Breast Cancer Carcinogenesis
[Proceedings of the National Academy of Sciences of the United States of America] Researchers demonstrated that FRS2β, an adaptor protein expressed in a small subset of epithelial cells, triggered the proinflammatory changes that induced stroma in premalignant mammary tissues and was responsible for the disease onset.
Intestinal Cell News
Complete Loss of miR-200 Family Induces EMT Associated Cellular Senescence in Gastric Cancer
[Oncogene] Genetic deletion of all miR-200s in the human gastric cancer cell lines induced potent morphological alterations, G1/S cell cycle arrest, increased senescence-associated β-galactosidase activity, and aberrant metabolism, collectively resembling the senescent phenotype.