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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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.
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•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 |
format | Article |
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[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.</description><identifier>ISSN: 0898-6568</identifier><identifier>EISSN: 1873-3913</identifier><identifier>DOI: 10.1016/j.cellsig.2016.12.003</identifier><identifier>PMID: 27940051</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>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</subject><ispartof>Cellular signalling, 2017-01, Vol.30, p.162-170</ispartof><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-5568205c88105ad1c54d273efb67d0d08e38332e87f8b982c2f780818bfbcce73</citedby><cites>FETCH-LOGICAL-c365t-5568205c88105ad1c54d273efb67d0d08e38332e87f8b982c2f780818bfbcce73</cites><orcidid>0000-0002-6303-481X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.cellsig.2016.12.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27940051$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cerezo, David</creatorcontrib><creatorcontrib>Ruiz-Alcaraz, Antonio J.</creatorcontrib><creatorcontrib>Lencina-Guardiola, Miriam</creatorcontrib><creatorcontrib>Cánovas, Manuel</creatorcontrib><creatorcontrib>García-Peñarrubia, Pilar</creatorcontrib><creatorcontrib>Martínez-López, Inmaculada</creatorcontrib><creatorcontrib>Martín-Orozco, Elena</creatorcontrib><title>Attenuated JNK signaling in multidrug-resistant leukemic cells. Dual role of MAPK in cell survival</title><title>Cellular signalling</title><addtitle>Cell Signal</addtitle><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.</description><subject>Animals</subject><subject>ATP-Binding Cassette, Sub-Family B, Member 1 - metabolism</subject><subject>Cell Line, Tumor</subject><subject>Cell Survival - drug effects</subject><subject>Cold Temperature</subject><subject>Cold-stress</subject><subject>Collateral sensitivity</subject><subject>Drug Resistance, Multiple</subject><subject>Drug Resistance, Neoplasm</subject><subject>Extracellular Signal-Regulated MAP Kinases - metabolism</subject><subject>Humans</subject><subject>JNK Mitogen-Activated Protein Kinases - metabolism</subject><subject>Leukemia - enzymology</subject><subject>Leukemia - pathology</subject><subject>Leukemic cells</subject><subject>MAP Kinase Signaling System - drug effects</subject><subject>MAPK</subject><subject>MDR</subject><subject>Mice</subject><subject>Models, Biological</subject><subject>P-glycoprotein</subject><subject>Phosphorylation - drug effects</subject><subject>Protein Kinase Inhibitors - pharmacology</subject><subject>Transfection</subject><issn>0898-6568</issn><issn>1873-3913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkElv2zAQhYkiReMk_QkteMxFCpeQok-FkaXZ2uaQnAmKHBl0KCnlYqD_vlLt5NrTYDDvzZv5EPpCSU0JlWeb2kIIya9rNrU1ZTUh_ANaUNXwii8pP0ALopaqkkKqQ3SU0oYQKohkn9Aha5bnhAi6QO0qZxiKyeDw3c97PC0cTPDDGvsB9yVk72JZVxGST9kMGQcoL9B7i__F1_iymIDjGACPHf6xeryfjfMMpxK3fmvCCfrYmZDg874eo-frq6eLm-rh1_fbi9VDZbkUuRLTnYwIqxQlwjhqxbljDYeulY0jjijginMGqulUu1TMsq5RRFHVdq210PBjdLrb-xrH3wVS1r1P8yVmgLEkTZVgUkol6CQVO6mNY0oROv0afW_iH02JnvHqjd7j1TNeTZme8E6-r_uI0vbg3l1vPCfBt50Apke3HqJO1sNgwfkINms3-v9E_AUPpo3z</recordid><startdate>201701</startdate><enddate>201701</enddate><creator>Cerezo, David</creator><creator>Ruiz-Alcaraz, Antonio J.</creator><creator>Lencina-Guardiola, Miriam</creator><creator>Cánovas, Manuel</creator><creator>García-Peñarrubia, Pilar</creator><creator>Martínez-López, Inmaculada</creator><creator>Martín-Orozco, Elena</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6303-481X</orcidid></search><sort><creationdate>201701</creationdate><title>Attenuated JNK signaling in multidrug-resistant leukemic cells. Dual role of MAPK in cell survival</title><author>Cerezo, David ; Ruiz-Alcaraz, Antonio J. ; Lencina-Guardiola, Miriam ; Cánovas, Manuel ; García-Peñarrubia, Pilar ; Martínez-López, Inmaculada ; Martín-Orozco, Elena</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-5568205c88105ad1c54d273efb67d0d08e38332e87f8b982c2f780818bfbcce73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>ATP-Binding Cassette, Sub-Family B, Member 1 - metabolism</topic><topic>Cell Line, Tumor</topic><topic>Cell Survival - drug effects</topic><topic>Cold Temperature</topic><topic>Cold-stress</topic><topic>Collateral sensitivity</topic><topic>Drug Resistance, Multiple</topic><topic>Drug Resistance, Neoplasm</topic><topic>Extracellular Signal-Regulated MAP Kinases - metabolism</topic><topic>Humans</topic><topic>JNK Mitogen-Activated Protein Kinases - metabolism</topic><topic>Leukemia - enzymology</topic><topic>Leukemia - pathology</topic><topic>Leukemic cells</topic><topic>MAP Kinase Signaling System - drug effects</topic><topic>MAPK</topic><topic>MDR</topic><topic>Mice</topic><topic>Models, Biological</topic><topic>P-glycoprotein</topic><topic>Phosphorylation - drug effects</topic><topic>Protein Kinase Inhibitors - pharmacology</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cerezo, David</creatorcontrib><creatorcontrib>Ruiz-Alcaraz, Antonio J.</creatorcontrib><creatorcontrib>Lencina-Guardiola, Miriam</creatorcontrib><creatorcontrib>Cánovas, Manuel</creatorcontrib><creatorcontrib>García-Peñarrubia, Pilar</creatorcontrib><creatorcontrib>Martínez-López, Inmaculada</creatorcontrib><creatorcontrib>Martín-Orozco, Elena</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cellular signalling</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cerezo, David</au><au>Ruiz-Alcaraz, Antonio J.</au><au>Lencina-Guardiola, Miriam</au><au>Cánovas, Manuel</au><au>García-Peñarrubia, Pilar</au><au>Martínez-López, Inmaculada</au><au>Martín-Orozco, Elena</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Attenuated JNK signaling in multidrug-resistant leukemic cells. Dual role of MAPK in cell survival</atitle><jtitle>Cellular signalling</jtitle><addtitle>Cell Signal</addtitle><date>2017-01</date><risdate>2017</risdate><volume>30</volume><spage>162</spage><epage>170</epage><pages>162-170</pages><issn>0898-6568</issn><eissn>1873-3913</eissn><abstract>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.</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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