Tag results:

STAT3

gp130 Cytokines Activate Novel Signaling Pathways and Alter Bone Dissemination in ER+ Breast Cancer Cells

[Journal of Bone and Mineral Research] In estrogen receptor positive (ER+) cells, oncostatin M (OSM) robustly stimulated phosphorylation of known gp130 signaling targets STAT3, ERK and AKT, while CNTF activated STAT3 signaling. In ER- breast cancer cells, OSM alone stimulated AKT and ERK signaling.

Expansion of Monocytic Myeloid-Derived Suppressor Cells Ameliorated Intestinal Inflammatory Response by Radiation through SOCS3 Expression

[Cell Death & Disease] Scientists demonstrated that radiation exposure in mice promoted the expansion of splenic and intestinal myeloid-derived suppressor cells and caused intestinal inflammation due to the increased secretion of cytokines.

SHOX2 Cooperates with STAT3 to Promote Breast Cancer Metastasis through the Transcriptional Activation of WASF3

[Journal of Experimental & Clinical Cancer Research] TCGA analysis was performed to identify the clinical relevance of short stature homeobox 2 (SHOX2) in breast cancer. Molecular regulations and alterations were assessed by Western blotting, immunoprecipitation, immunohistochemistry, qRT-PCR, chromatin immunoprecipitation coupled with qPCR, and ChIP/re-ChIP.

Transcriptional Control of Brain Tumor Stem Cells by a Carbohydrate Binding Protein

[Cell Reports] The authors reported that the LGALS1 gene, encoding the carbohydrate binding protein, galectin1, is a key regulator of brain tumor stem cells and glioblastoma resistance to therapy.

circPTPN22 Attenuates Immune Microenvironment of Pancreatic Cancer via STAT3 Acetylation

[Cancer Gene Therapy] Cell counting kit-8 assay and colony formation assay were used to measure the proliferation of pancreatic cancer cells. RNA immunoprecipitation and Western blot were employed for investigation the binding between circPTPN22 and STAT3.

Redundant Cytokine Requirement for Intestinal Microbiota-Induced Th17 Cell Differentiation in Draining Lymph Nodes

[Cell Reports] Scientists showed that intestine-draining mesenteric lymph nodes, not intestine proper, were the dominant site of segmented filamentous bacteria-induced intestinal Th17 cell differentiation.

Popular