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Metabolic Glycoengineering Sensitizes Drug-Resistant Pancreatic Cancer Cells to Tyrosine Kinase Inhibitors Erlotinib and Gefitinib
Metastatic human pancreatic cancer cells (the SW1990 line) that are resistant to the EGFR-targeting tyrosine kinase inhibitor drugs (TKI) erlotinib and gefitinib were treated with 1,3,4-O-Bu(3)ManNAc, a “metabolic glycoengineering” drug candidate that increased sialylation by ∼12-fold. Consistent wi...
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| Foilsithe in: | Bioorg Med Chem Lett |
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| Main Authors: | , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2015
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5753412/ https://ncbi.nlm.nih.gov/pubmed/25690786 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmcl.2015.01.060 |
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