Overexpression of Tpl2 is linked to imatinib resistance and activation of MEK‐ERK and NF‐κB pathways in a model of chronic myeloid leukemia. Issue 5 (6th April 2018)

• Record Type: Journal Article
• Authors: Chorzalska, Anna; Ahsan, Nagib; Rao, R. Shyama Prasad; Roder, Karim; Yu, Xiaoqing; Morgan, John; Tepper, Alexander; Hines, Steven; Zhang, Peng; Treaba, Diana O.; Zhao, Ting C.; Olszewski, Adam J.; Reagan, John L.; Liang, Olin; Gruppuso, Philip A.; Dubielecka, Patrycja M.
• Is Part Of: Molecular oncology. Volume 12:Issue 5(2018)
• Page Start: 630
• Page End: 647
• Publication Date: 2018-04-06
• Subjects: Bcr‐Abl1 -- COT1 -- imatinib resistance -- Map3k8 -- stem cells -- Tpl2; Cancer -- Molecular aspects -- Periodicals; 616.994005
• DOI: 10.1002/1878-0261.12186
• Languages: English
• ISSNs: 1574-7891

Abstract

Abstract : The introduction of tyrosine kinase inhibitors (TKI) has transformed chronic myeloid leukemia (CML) into a chronic disease with long‐term survival exceeding 85%. However, resistance of CML stem cells to TKI may contribute to the 50% relapse rate observed after TKI discontinuation in molecular remission. We previously described a model of resistance to imatinib mesylate (IM), in which K562 cells cultured in high concentrations of imatinib mesylate showed reduced Bcr‐Abl1 protein and activity levels while maintaining proliferative potential. Using quantitative phosphoproteomic analysis of these IM‐resistant cells, we have now identified significant upregulation of tumor progression locus (Tpl2), also known as cancer Osaka thyroid (COT1) kinase or Map3k8. Overexpression of Tpl2 in IM‐resistant cells was accompanied by elevated activities of Src family kinases (SFKs) and NF‐κB, MEK‐ERK signaling. CD34+ cells isolated from the bone marrow of patients with CML and exposed to IM in vitro showed increased MAP3K8 transcript levels. Dasatinib (SFK inhibitor), U0126 (MEK inhibitor), and PS‐1145 (IκB kinase (IKK) inhibitor) used in combination resulted in elimination of 65% of IM‐resistant cells and reduction in the colony‐forming capacity of CML CD34+ cells in methylcellulose assays by 80%. In addition, CML CD34+ cells cultured with the combination of inhibitors showed reduced MAP3K8 transcript levels. Overall, our data indicate that elevated Tpl2 protein and transcript levels are associated with resistance to IM and that combined inhibition of SFK, MEK, and NF‐κB signaling attenuates the survival of IM‐resistant CML cells and CML CD34+ cells. Therefore, combination of SFK, MEK, and NF‐κB inhibitors may offer a new therapeutic approach to overcome TKI resistance in CML patients. Abstract : The current consensus is that rare leukemic stem cells (LSC) are insensitive to chemotherapy and are the cause of leukemia recurrence. The molecular mechanisms responsible for LSC chemoresistance are not fully understood. In this manuscript, we report that overexpression of Tpl2 (also known as Map3k8 or COT1) is linked to overactive MEK‐ERK and NF‐κB signaling and confers insensitivity to imatinib mesylate (IM) in CML stem cells and in cellular model of Bcr‐Abl1‐independent IM resistance.