Attenuated JNK signaling in multidrug-resistant leukemic cells. Dual role of MAPK in cell survival

Having found previously that leukemic cells with multidrug resistant (MDR) phenotype, but not their sensitive counterparts, exhibit collateral sensitivity to cold stress in a P-gp-dependent manner, our aim was to study the signaling pathways involved in this phenomenon in sensitive (L1210) and resis...

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Veröffentlicht in:Cellular signalling 2017-01, Vol.30, p.162-170
Hauptverfasser: Cerezo, David, Ruiz-Alcaraz, Antonio J., Lencina-Guardiola, Miriam, Cánovas, Manuel, García-Peñarrubia, Pilar, Martínez-López, Inmaculada, Martín-Orozco, Elena
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container_end_page 170
container_issue
container_start_page 162
container_title Cellular signalling
container_volume 30
creator Cerezo, David
Ruiz-Alcaraz, Antonio J.
Lencina-Guardiola, Miriam
Cánovas, Manuel
García-Peñarrubia, Pilar
Martínez-López, Inmaculada
Martín-Orozco, Elena
description Having found previously that leukemic cells with multidrug resistant (MDR) phenotype, but not their sensitive counterparts, exhibit collateral sensitivity to cold stress in a P-gp-dependent manner, our aim was to study the signaling pathways involved in this phenomenon in sensitive (L1210) and resistant cells (L1210R and CBMC-6). It was observed that the acquisition of MDR phenotype by leukemic cells or their transfection with the extrussion pump, P-gp, modifies the activation profile and regulation of Mitogen-Activated Protein Kinases (MAPK) in cells exposed to low temperatures. More specifically, cold stress provoked the activation of c-Jun N-terminal kinase (JNK) in sensitive cells, while attenuated JNK signaling was observed in MDR cells. This effect was also observed, although with less intensity, in P-gp-transfected cells. Using pharmacological inhibitors to determine the role of MAPK in leukemic cell survival in physiological conditions or under cold stress, a dual temperature-dependent role was observed for JNK in MDR cell survival. At 37°C JNK is necessary for the survival of parental, resistant and P-gp-transfected cells; however, the use of inhibitors of either extracellular signal-regulated protein kinase (ERK) or JNK significantly counteracts cold-induced death of resistant and P-gp-transfected cells, supporting a role for ERK and JNK in cold-stress induced cell death. Finally, a connectivity model concerning MAPK is proposed, summarizing how cold stress and MDR-1 might trigger apoptosis in resistant cell lines. These findings on MDR cells may assist in the design of specific therapeutic strategies to complement current chemotherapy. [Display omitted] •Cold stress-induces collateral sensitivity in MDR leukemic cells.•P-gp, modifies the activation profile of MAPK in leukemic cells under hypothermia.•P-gp-expressing cells show attenuated JNK signaling under cold stress conditions.•JNK and ERK exert a temperature-dependent dual role in MDR cells survival.•A dynamic model featuring a JNK-positive feedback loop is proposed.
doi_str_mv 10.1016/j.cellsig.2016.12.003
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More specifically, cold stress provoked the activation of c-Jun N-terminal kinase (JNK) in sensitive cells, while attenuated JNK signaling was observed in MDR cells. This effect was also observed, although with less intensity, in P-gp-transfected cells. Using pharmacological inhibitors to determine the role of MAPK in leukemic cell survival in physiological conditions or under cold stress, a dual temperature-dependent role was observed for JNK in MDR cell survival. At 37°C JNK is necessary for the survival of parental, resistant and P-gp-transfected cells; however, the use of inhibitors of either extracellular signal-regulated protein kinase (ERK) or JNK significantly counteracts cold-induced death of resistant and P-gp-transfected cells, supporting a role for ERK and JNK in cold-stress induced cell death. Finally, a connectivity model concerning MAPK is proposed, summarizing how cold stress and MDR-1 might trigger apoptosis in resistant cell lines. These findings on MDR cells may assist in the design of specific therapeutic strategies to complement current chemotherapy. [Display omitted] •Cold stress-induces collateral sensitivity in MDR leukemic cells.•P-gp, modifies the activation profile of MAPK in leukemic cells under hypothermia.•P-gp-expressing cells show attenuated JNK signaling under cold stress conditions.•JNK and ERK exert a temperature-dependent dual role in MDR cells survival.•A dynamic model featuring a JNK-positive feedback loop is proposed.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>27940051</pmid><doi>10.1016/j.cellsig.2016.12.003</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6303-481X</orcidid></addata></record>
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subjects Animals
ATP-Binding Cassette, Sub-Family B, Member 1 - metabolism
Cell Line, Tumor
Cell Survival - drug effects
Cold Temperature
Cold-stress
Collateral sensitivity
Drug Resistance, Multiple
Drug Resistance, Neoplasm
Extracellular Signal-Regulated MAP Kinases - metabolism
Humans
JNK Mitogen-Activated Protein Kinases - metabolism
Leukemia - enzymology
Leukemia - pathology
Leukemic cells
MAP Kinase Signaling System - drug effects
MAPK
MDR
Mice
Models, Biological
P-glycoprotein
Phosphorylation - drug effects
Protein Kinase Inhibitors - pharmacology
Transfection
title Attenuated JNK signaling in multidrug-resistant leukemic cells. Dual role of MAPK in cell survival
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