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Potent EMT and CSC Phenotypes Are Induced By Oncostatin-M in Pancreatic Cancer.

Molecular cancer research : MCR (2017-01-06)
Jacob M Smigiel, Neetha Parameswaran, Mark W Jackson
RÉSUMÉ

Pancreatic ductal adenocarcinoma (PDAC) is referred to as a silent killer due to the lack of clear symptoms, a lack of early detection methods, and a high frequency of metastasis at diagnosis. In addition, pancreatic cancer is remarkably resistant to chemotherapy, and clinical treatment options remain limited. The tumor microenvironment (TME) and associated factors are important determinants of metastatic capacity and drug resistance. Here, oncostatin M (OSM), an IL6 cytokine family member, was identified as an important driver of mesenchymal and cancer stem cell (CSC) phenotypes. Furthermore, the generation of cells that harbor mesenchymal/CSC properties following OSM exposure resulted in enhanced tumorigenicity, increased metastasis, and resistance to gemcitabine. OSM induced the expression of

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Sigma-Aldrich
apo-Transferrine human, ≥95% protein basis (biuret)