Please use this identifier to cite or link to this item:
|Title:||Targeting translation factors in haematologic malignancies.||Authors:||Lee, Janice Siu Hui.||Keywords:||DRNTU::Science::Biological sciences||Issue Date:||2011||Abstract:||Imatinib resistance arose in patients with chronic myeloid leukaemia (CML) due to the alterations in the BCR-ABL kinase domain. It was established that the elevated β-catenin activation led to the progression of CML from chronic phase to blast crisis phase. Inhibition of phosphorylated eIF4E (p-eIF4E) was found to avert the activation of β-catenin. The goals of this project were to establish the relationship between p-eIF4E and β-catenin activation, to contrast the effects of drugs sorafenib and imatinib in reducing the amount of β-catenin activation and to investigate if the inhibitory effects of sorafenib on p-eIF4E were specifically via the inhibition of Mnk 1/2. Effects of drug treatments on K562 and HL-60 cell lines were analysed using western blots, TOP-flash assays and immunofluorescence assays. Unlike imatinib, sorafenib was able to inhibit the p-eIF4E (P value<0.05). A positive correlation was found between p-eIF4E and β-catenin activation (P value<0.05). Compared to imatinib, 10μM of sorafenib was able to significantly reduce the amount of β-catenin activation via the inhibition of p-eIF4E (P value <0.005). Sorafenib not only acts as an alternative for imatinib, it might significantly reduce the β-catenin activation specifically found in leukemic stem cells, preventing the progression of CML and other haematologic malignancies.||URI:||http://hdl.handle.net/10356/44751||Rights:||Nanyang Technological University||Fulltext Permission:||restricted||Fulltext Availability:||With Fulltext|
|Appears in Collections:||SBS Student Reports (FYP/IA/PA/PI)|
Files in This Item:
|Targeting translation factors in haematologic malignancies.pdf|
|1.85 MB||Adobe PDF||View/Open|
Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.