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EMT

MiR-199 Reverses the Resistance to Gemcitabine in Pancreatic Cancer by Suppressing Stemness through Regulating the Epithelial–Mesenchymal Transition

[ACS Omega] Researchers investigate the function of miR-199 on gemcitabine-resistance in pancreatic cancer, as well as the underlying mechanism.

The Isoflavone Puerarin Exerts Anti-Tumor Activity in Pancreatic Ductal Adenocarcinoma by Suppressing mTOR-Mediated Glucose Metabolism

[Aging] The tumor-suppressive effects of puerarin were determined by both in vitro and in vivo assays. The effects of puerarin on the proliferation, apoptosis, migration and invasion of pancreatic cancer cells, and tumor growth and metastasis in pancreatic ductal adenocarcinoma xenograft mouse model were performed.

SPOCK1 Promotes Metastasis in Pancreatic Cancer via NF-κB-Dependent Epithelial-Mesenchymal Transition by Interacting with IκB-α

[Cellular Oncology] Scientists evaluated the expression and clinicopathological significance of sparc/osteonectin, cwcv and kazal-like domain proteoglycan 1 (SPOCK1) in primary pancreatic cancer (PC) specimens and explored the mechanisms underlying SPOCK1-mediated PC cell growth and metastasis.

Mesenchymal Stromal Cells Mitigate Liver Damage after Extended Resection in the Pig by Modulating Thrombospondin-1/TGF-β

[NPJ Regenerative Medicine] The authors suggested that mesenchymal stromal cells ameliorated surgery-induced hepatocellular stress and epithelial-mesenchymal transition, thus supporting epithelial integrity and facilitating regeneration.

Hsa_circ_0030586 Promotes Epithelial–Mesenchymal Transition in Prostate Cancer via PI3K-AKT Signaling

[Bioengineered] Investigators showed that hsa_circ_0030586 was significantly upregulated in prostate cancer (PCa) cells. Interfering with hsa_circ_0030586 in PC3 cells inhibited cell proliferation, migration, and invasion.

SMAD4 Mutations Do Not Preclude Epithelial–Mesenchymal Transition in Colorectal Cancer

[Oncogene] It was widely assumed that SMAD4-mutant (SMAD4mut) cancer cells were unable to undergo epithelial-mesenchymal transition (EMT). Researchers scrutinized this notion and probed for potential SMAD4-independent EMT execution using SMAD4mut colorectal cancer cell lines.

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