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survivin

STAT3/SH3PXD2A-AS1/miR-125b/STAT3 Positive Feedback Loop Affects Psoriasis Pathogenesis via Regulating Human Keratinocyte Proliferation

[Cytokine] SH3PXD2A-AS1 silence was found to suppress HaCaT cell proliferation and promote HaCaT cell apoptosis significantly. Meanwhile, SH3PXD2A-AS1 silence significantly increased cleaved-caspase-3 protein levels and inhibited S100A7, TNF-α, IL-6, p-STAT3, STAT3, CyclinD1, and survivin protein levels.

Bone Marrow Mesenchymal Stromal Cells can Render Multiple Myeloma Cells Resistant to Cytotoxic Machinery of CAR T Cells through Inhibition of Apoptosis

[Clinical Cancer Research] Scientists investigated the significance of this mode of immune-escape on T cells engineered to express chimeric antigen receptors (CAR-T) cells.

Lupeol Induces Autophagy and Apoptosis with Reduced Cancer Stem-Like Properties in Retinoblastoma via Phosphoinositide 3-Kinase/Protein Kinase B/Mammalian Target of Rapamycin Inhibition

[Journal of Pharmacy and Pharmacology] Lupeol could also inhibit proliferation and induce apoptosis of retinoblastoma cells, with increased Bax level and decreased Ki67, survivin and Bcl-2 levels.

A CRISPR/Cas9-Engineered ARID1A-Deficient Human Gastric Cancer Organoid Model Reveals Essential and Non-Essential Modes of Oncogenic Transformation

[Cancer Discovery] CRISPR/Cas9-mediated ARID1A knockout in primary TP53-/- human gastric organoids induced morphologic dysplasia, tumorigenicity and mucinous differentiation.

In Silico and In Vitro Studies on the Anti-Cancer Activity of Andrographolide Targeting Survivin in Human Breast Cancer Stem Cells

[PLoS One] Human CD24-/CD44+ breast cancer stem cells (BCSCs) were treated with andrographolide in vitro for 24 hours. The cytotoxic effect of andrographolide on BCSCs was compared to that on human mesenchymal stem cells.

Acetyl-Bufalin Shows Potent Efficacy against Non-Small-Cell Lung Cancer by Targeting the CDK9/STAT3 Signaling Pathway

[British Journal of Cancer] Researchers showed that CDK9 induced non-small-cell lung cancer cell proliferation and that this effect was associated with STAT3 activation, specifically an increase in STAT3 phosphorylation and transcription factor activity.

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