Loading…

Characterization of the Role of the Malate Dehydrogenases to Lung Tumor Cell Survival

Cellular compartmentalization of biochemical processes in eukaryotic cells is critical for many functions including shuttling of reducing equivalents across membranes. Although coordination of metabolic flux between different organelles is vital for cell physiology, its impact on tumor cell survival...

Full description

Saved in:
Bibliographic Details
Published in:Journal of Cancer 2017-01, Vol.8 (11), p.2088-2096
Main Authors: Zhang, Boxi, Tornmalm, Johan, Widengren, Jerker, Vakifahmetoglu-Norberg, Helin, Norberg, Erik
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c501t-7d3992b5f8b5324a80ff0e4bc06b02d3026d5e2b7d568591c9a899a53af1e9043
cites
container_end_page 2096
container_issue 11
container_start_page 2088
container_title Journal of Cancer
container_volume 8
creator Zhang, Boxi
Tornmalm, Johan
Widengren, Jerker
Vakifahmetoglu-Norberg, Helin
Norberg, Erik
description Cellular compartmentalization of biochemical processes in eukaryotic cells is critical for many functions including shuttling of reducing equivalents across membranes. Although coordination of metabolic flux between different organelles is vital for cell physiology, its impact on tumor cell survival is not well understood. By using an integrative approach, we have dissected the role of the key metabolic enzymes Malate dehydrogenases (MDH1 and MDH2) to the survival of Non-small Cell Lung Carcinomas. Here, we report that while both the MDH1 (cytosolic) and the MDH2 (mitochondrial) enzymes display elevated levels in patients compared to normal counterparts, only high expression of MDH1 is associated with poor prognosis. We further show that the MDH1 enzymatic activity is significantly higher in NSCLC cells than that of MDH2. Accordingly, genetic depletion of MDH1 leads to significantly higher toxicity than depletion of MDH2. These findings provide molecular insights into the metabolic characteristics of the malate isoenzymes and mark MDH1 as a potential therapeutic target in these tumors.
doi_str_mv 10.7150/jca.19373
format article
fullrecord <record><control><sourceid>proquest_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_swepub_ki_se_494674</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1930483200</sourcerecordid><originalsourceid>FETCH-LOGICAL-c501t-7d3992b5f8b5324a80ff0e4bc06b02d3026d5e2b7d568591c9a899a53af1e9043</originalsourceid><addsrcrecordid>eNp9ks1O3DAUhS3UCtCURV8AedkuQv0b2xskNECLNFUlCt1aTnIzCWTiqe0Mok_fDDNDYVG88ZH93Xss34PQR0pOFJXky13pTqjhiu-hQ6q5ykyei3cv9AE6ivGOjIsbpgTfRwdMa2oEJYfodtq44MoEof3jUut77GucGsDXvoOd_u46lwCfQ_NYBT-H3kWIOHk8G_o5vhkWPuApdB3-OYRVu3LdB_S-dl2Eo-0-QbeXFzfTb9nsx9er6dksKyWhKVMVN4YVstaF5Ew4TeqagChKkheEVZywvJLAClXJXEtDS-O0MU5yV1MwRPAJyjZ94wMsh8IuQ7tw4dF619rt0f2owAojcrXmzX_5ZfDVv6JdIeU5V1IT-qbXefvrzPowt_epsYxSLddepxt-hBdQldCn4LrXlq9u-raxc7-yUkpj1Nrw07ZB8L8HiMku2liO3-x68EO049CJ0JyNc52gzxu0DD7GAPWzDSV2nRI7psQ-pWRkj1--65ncZYL_Bd0buc4</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1930483200</pqid></control><display><type>article</type><title>Characterization of the Role of the Malate Dehydrogenases to Lung Tumor Cell Survival</title><source>PubMed Central</source><creator>Zhang, Boxi ; Tornmalm, Johan ; Widengren, Jerker ; Vakifahmetoglu-Norberg, Helin ; Norberg, Erik</creator><creatorcontrib>Zhang, Boxi ; Tornmalm, Johan ; Widengren, Jerker ; Vakifahmetoglu-Norberg, Helin ; Norberg, Erik</creatorcontrib><description>Cellular compartmentalization of biochemical processes in eukaryotic cells is critical for many functions including shuttling of reducing equivalents across membranes. Although coordination of metabolic flux between different organelles is vital for cell physiology, its impact on tumor cell survival is not well understood. By using an integrative approach, we have dissected the role of the key metabolic enzymes Malate dehydrogenases (MDH1 and MDH2) to the survival of Non-small Cell Lung Carcinomas. Here, we report that while both the MDH1 (cytosolic) and the MDH2 (mitochondrial) enzymes display elevated levels in patients compared to normal counterparts, only high expression of MDH1 is associated with poor prognosis. We further show that the MDH1 enzymatic activity is significantly higher in NSCLC cells than that of MDH2. Accordingly, genetic depletion of MDH1 leads to significantly higher toxicity than depletion of MDH2. These findings provide molecular insights into the metabolic characteristics of the malate isoenzymes and mark MDH1 as a potential therapeutic target in these tumors.</description><identifier>ISSN: 1837-9664</identifier><identifier>EISSN: 1837-9664</identifier><identifier>DOI: 10.7150/jca.19373</identifier><identifier>PMID: 28819410</identifier><language>eng</language><publisher>Australia: Ivyspring International Publisher</publisher><subject>Cancer Metabolism ; Lung Cancer ; Malate dehydrogenase ; Medicin och hälsovetenskap ; Research Paper</subject><ispartof>Journal of Cancer, 2017-01, Vol.8 (11), p.2088-2096</ispartof><rights>Ivyspring International Publisher 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c501t-7d3992b5f8b5324a80ff0e4bc06b02d3026d5e2b7d568591c9a899a53af1e9043</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559971/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559971/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28819410$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-211854$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:136375801$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Boxi</creatorcontrib><creatorcontrib>Tornmalm, Johan</creatorcontrib><creatorcontrib>Widengren, Jerker</creatorcontrib><creatorcontrib>Vakifahmetoglu-Norberg, Helin</creatorcontrib><creatorcontrib>Norberg, Erik</creatorcontrib><title>Characterization of the Role of the Malate Dehydrogenases to Lung Tumor Cell Survival</title><title>Journal of Cancer</title><addtitle>J Cancer</addtitle><description>Cellular compartmentalization of biochemical processes in eukaryotic cells is critical for many functions including shuttling of reducing equivalents across membranes. Although coordination of metabolic flux between different organelles is vital for cell physiology, its impact on tumor cell survival is not well understood. By using an integrative approach, we have dissected the role of the key metabolic enzymes Malate dehydrogenases (MDH1 and MDH2) to the survival of Non-small Cell Lung Carcinomas. Here, we report that while both the MDH1 (cytosolic) and the MDH2 (mitochondrial) enzymes display elevated levels in patients compared to normal counterparts, only high expression of MDH1 is associated with poor prognosis. We further show that the MDH1 enzymatic activity is significantly higher in NSCLC cells than that of MDH2. Accordingly, genetic depletion of MDH1 leads to significantly higher toxicity than depletion of MDH2. These findings provide molecular insights into the metabolic characteristics of the malate isoenzymes and mark MDH1 as a potential therapeutic target in these tumors.</description><subject>Cancer Metabolism</subject><subject>Lung Cancer</subject><subject>Malate dehydrogenase</subject><subject>Medicin och hälsovetenskap</subject><subject>Research Paper</subject><issn>1837-9664</issn><issn>1837-9664</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9ks1O3DAUhS3UCtCURV8AedkuQv0b2xskNECLNFUlCt1aTnIzCWTiqe0Mok_fDDNDYVG88ZH93Xss34PQR0pOFJXky13pTqjhiu-hQ6q5ykyei3cv9AE6ivGOjIsbpgTfRwdMa2oEJYfodtq44MoEof3jUut77GucGsDXvoOd_u46lwCfQ_NYBT-H3kWIOHk8G_o5vhkWPuApdB3-OYRVu3LdB_S-dl2Eo-0-QbeXFzfTb9nsx9er6dksKyWhKVMVN4YVstaF5Ew4TeqagChKkheEVZywvJLAClXJXEtDS-O0MU5yV1MwRPAJyjZ94wMsh8IuQ7tw4dF619rt0f2owAojcrXmzX_5ZfDVv6JdIeU5V1IT-qbXefvrzPowt_epsYxSLddepxt-hBdQldCn4LrXlq9u-raxc7-yUkpj1Nrw07ZB8L8HiMku2liO3-x68EO049CJ0JyNc52gzxu0DD7GAPWzDSV2nRI7psQ-pWRkj1--65ncZYL_Bd0buc4</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Zhang, Boxi</creator><creator>Tornmalm, Johan</creator><creator>Widengren, Jerker</creator><creator>Vakifahmetoglu-Norberg, Helin</creator><creator>Norberg, Erik</creator><general>Ivyspring International Publisher</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8V</scope><scope>D8T</scope><scope>ZZAVC</scope></search><sort><creationdate>20170101</creationdate><title>Characterization of the Role of the Malate Dehydrogenases to Lung Tumor Cell Survival</title><author>Zhang, Boxi ; Tornmalm, Johan ; Widengren, Jerker ; Vakifahmetoglu-Norberg, Helin ; Norberg, Erik</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c501t-7d3992b5f8b5324a80ff0e4bc06b02d3026d5e2b7d568591c9a899a53af1e9043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Cancer Metabolism</topic><topic>Lung Cancer</topic><topic>Malate dehydrogenase</topic><topic>Medicin och hälsovetenskap</topic><topic>Research Paper</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Boxi</creatorcontrib><creatorcontrib>Tornmalm, Johan</creatorcontrib><creatorcontrib>Widengren, Jerker</creatorcontrib><creatorcontrib>Vakifahmetoglu-Norberg, Helin</creatorcontrib><creatorcontrib>Norberg, Erik</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Kungliga Tekniska Högskolan</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>Journal of Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Boxi</au><au>Tornmalm, Johan</au><au>Widengren, Jerker</au><au>Vakifahmetoglu-Norberg, Helin</au><au>Norberg, Erik</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of the Role of the Malate Dehydrogenases to Lung Tumor Cell Survival</atitle><jtitle>Journal of Cancer</jtitle><addtitle>J Cancer</addtitle><date>2017-01-01</date><risdate>2017</risdate><volume>8</volume><issue>11</issue><spage>2088</spage><epage>2096</epage><pages>2088-2096</pages><issn>1837-9664</issn><eissn>1837-9664</eissn><abstract>Cellular compartmentalization of biochemical processes in eukaryotic cells is critical for many functions including shuttling of reducing equivalents across membranes. Although coordination of metabolic flux between different organelles is vital for cell physiology, its impact on tumor cell survival is not well understood. By using an integrative approach, we have dissected the role of the key metabolic enzymes Malate dehydrogenases (MDH1 and MDH2) to the survival of Non-small Cell Lung Carcinomas. Here, we report that while both the MDH1 (cytosolic) and the MDH2 (mitochondrial) enzymes display elevated levels in patients compared to normal counterparts, only high expression of MDH1 is associated with poor prognosis. We further show that the MDH1 enzymatic activity is significantly higher in NSCLC cells than that of MDH2. Accordingly, genetic depletion of MDH1 leads to significantly higher toxicity than depletion of MDH2. These findings provide molecular insights into the metabolic characteristics of the malate isoenzymes and mark MDH1 as a potential therapeutic target in these tumors.</abstract><cop>Australia</cop><pub>Ivyspring International Publisher</pub><pmid>28819410</pmid><doi>10.7150/jca.19373</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1837-9664
ispartof Journal of Cancer, 2017-01, Vol.8 (11), p.2088-2096
issn 1837-9664
1837-9664
language eng
recordid cdi_swepub_primary_oai_swepub_ki_se_494674
source PubMed Central
subjects Cancer Metabolism
Lung Cancer
Malate dehydrogenase
Medicin och hälsovetenskap
Research Paper
title Characterization of the Role of the Malate Dehydrogenases to Lung Tumor Cell Survival
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T22%3A12%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Characterization%20of%20the%20Role%20of%20the%20Malate%20Dehydrogenases%20to%20Lung%20Tumor%20Cell%20Survival&rft.jtitle=Journal%20of%20Cancer&rft.au=Zhang,%20Boxi&rft.date=2017-01-01&rft.volume=8&rft.issue=11&rft.spage=2088&rft.epage=2096&rft.pages=2088-2096&rft.issn=1837-9664&rft.eissn=1837-9664&rft_id=info:doi/10.7150/jca.19373&rft_dat=%3Cproquest_swepu%3E1930483200%3C/proquest_swepu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c501t-7d3992b5f8b5324a80ff0e4bc06b02d3026d5e2b7d568591c9a899a53af1e9043%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1930483200&rft_id=info:pmid/28819410&rfr_iscdi=true