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MAPK

Selenium Nanoparticles with Various Morphology for Antiangiogenesis through bFGF-Mediated P13K/AKT Signaling Pathways

[Nanotechnology] Selenium nanoparticles could competitively inhibit the binding of bFGF to fibroblast growth factor receptor through direct binding to bFGF, down-regulate the expression of bFGF in HUVEC cells, and significantly reduce the MAPK/Erk and P13K/AKT pathways activation of signaling molecules to regulate HUVEC cell migration and angiogenesis.

PTPN3 Is a Potential Target for a New Cancer Immunotherapy That Has a Dual Effect of T Cell Activation and Direct Cancer Inhibition in...

[Translational Oncology] Experiments in a mouse xenograft model using allo lymphocytes showed that PTPN3 inhibition in small cell lung cancer cells enhanced the anti-tumor effect of phosphatase non-receptor type 3 (PTPN3)-suppressed activated lymphocytes.

M2 Macrophages, but Not M1 Macrophages, Support Megakaryopoiesis by Upregulating PI3K-AKT Pathway Activity

[Signal Transduction and Targeted Therapy] Aberrant bone marrow-M1/M2 MФ polarization, characterized by increased M1 MФs and decreased M2 MФs and accompanied by impaired megakaryopoiesis-supporting abilities, was found in patients with thrombocytopenia post-allotransplant.

Acrolein Contributes to Human Colorectal Tumorigenesis through the Activation of RAS-MAPK Pathway

[Scientific Reports] Scientists found that acrolein induced oncogenic transformation, including faster cell cycling, proliferation, sphere formation and cell migration, in fibroblast cells, and acrolein-induced DNA damages were higher in colorectal cancer (CRC) tumor tissues than in normal epithelial cells in CRC patients.

Deficiency of Myostatin Protects Skeletal Muscle Cells from Ischemia Reperfusion Injury

[Scientific Reports] Examining human specimens from free myocutaneous flap transfer demonstrated increased myostatin signaling and tissue damage in terms of apoptotic activity, cell death, tissue edema, and lipid peroxidation.

Cabozantinib Promotes Erythroid Differentiation in K562 Erythroleukemia Cells through Global Changes in Gene Expression and JNK Activation

[Cancer Gene Therapy] The authors reported that cabozantinib could promote differentiation in erythroid leukemia cells and found that K562 erythroid leukemia cells treated with 1 μM cabozantinib for 72 hours underwent erythroid lineage differentiation.

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