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EMT

Placental Extract Suppresses the Formation of Fibrotic Deposits by Tumor Necrosis Factor Alpha and Transforming Growth Factor Beta-Induced Epithelial–Mesenchymal Transition in ARPE-19 Cells

[BMC Research Notes] Scientists evaluated whether placental extract influences epithelial–mesenchymal transition (EMT) and fibrosis through cytokine-induced EMT in the retinal pigment epithelial cells, in vitro.

Single-Cell RNA Sequencing Reveals the Epithelial Cell Heterogeneity and Invasive Subpopulation in Human Bladder Cancer

[International Journal of Cancer] Investigators applied droplet-based single-cell RNA sequencing (scRNA-seq) to acquire transcriptional profiles of 36 619 single cells isolated from seven patients.

p32 Promotes Melanoma Progression and Metastasis by Targeting EMT Markers, Akt/PKB Pathway, and Tumor Microenvironment

[Cell Death & Disease] The authors identified the role of p32 in the malignancy of both murine and human melanoma and found that p32 knockdown led to reduced cell proliferation, migration, and invasion in murine and human melanoma cells.

CKB Inhibits Epithelial-Mesenchymal Transition and Prostate Cancer Progression by Sequestering and Inhibiting AKT Activation

[Neoplasia] Scientists discovered that brain-type creatine kinase (CKB) was a negative regulator of epithelial-mesenchymal transition and AKT activation, which revealed a new mode of their regulation.

EIF4A3-Induced Circular RNA PRKAR1B Promotes Osteosarcoma Progression by miR-361-3p-Mediated Induction of FZD4 Expression

[Cell Death & Disease] Investigators found that circPRKAR1B enhanced osteosarcoma (OS) cell proliferation, migration, and promoted OS epithelial–mesenchymal transition.

AnnexinA7 Promotes Epithelial–Mesenchymal Transition by Interacting with Sorcin and Contributes to Aggressiveness in Hepatocellular Carcinoma

[Cell Death & Disease] In vitro functional investigations revealed that the interaction between AnnexinA7 and Sorcin regulated epithelial–mesenchymal transition, and then affected migration, invasion, and proliferation in hepatocellular carcinoma cells.

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