Suppression of MTHFD2 in MCF‑7 Breast Cancer Cells Increases Glycolysis, Dependency on Exogenous Glycine, and Sensitivity to Folate Depletion
Methylenetetrahydrofolate dehydrogenase (NAD(P)+ dependent) 2, methenyltetrahydrofolate cyclohydrolase (MTHFD2) is a mitochondrial enzyme involved in folate metabolism. A number of recent studies have highlighted this enzyme as being highly expressed in many solid tumors, including breast cancer, a...
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Veröffentlicht in: | Journal of proteome research 2016-08, Vol.15 (8), p.2618-2625 |
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creator | Koufaris, Costas Gallage, Suchira Yang, Tianlai Lau, Chung-Ho Valbuena, Gabriel N Keun, Hector C |
description | Methylenetetrahydrofolate dehydrogenase (NAD(P)+ dependent) 2, methenyltetrahydrofolate cyclohydrolase (MTHFD2) is a mitochondrial enzyme involved in folate metabolism. A number of recent studies have highlighted this enzyme as being highly expressed in many solid tumors, including breast cancer, and to be correlated with poor survival. However, the metabolic functions of MTHFD2 in cancer cells have not been well-defined. To investigate the function of MTHFD2 in breast cancer cells, we generated and characterized MCF-7 cells with stable suppression of MTHFD2 expression using a combination of cellular assays and metabolic profiling. Loss of MTHFD2 caused MCF7 cells to become glycine auxotrophs, that is, reliant on exogenous glycine, and more sensitive to exogenous folate depletion. Another prominent metabolic alteration observed as a consequence of MTHFD2 suppression was a more glycolytic phenotype, consistent with widespread modifications of cellular metabolism. Collectively, these data suggest that targeting MTHFD2 activity is likely to influence multiple metabolic pathways in breast cancer and could be combined with a range of antimetabolite therapies. |
doi_str_mv | 10.1021/acs.jproteome.6b00188 |
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A number of recent studies have highlighted this enzyme as being highly expressed in many solid tumors, including breast cancer, and to be correlated with poor survival. However, the metabolic functions of MTHFD2 in cancer cells have not been well-defined. To investigate the function of MTHFD2 in breast cancer cells, we generated and characterized MCF-7 cells with stable suppression of MTHFD2 expression using a combination of cellular assays and metabolic profiling. Loss of MTHFD2 caused MCF7 cells to become glycine auxotrophs, that is, reliant on exogenous glycine, and more sensitive to exogenous folate depletion. Another prominent metabolic alteration observed as a consequence of MTHFD2 suppression was a more glycolytic phenotype, consistent with widespread modifications of cellular metabolism. Collectively, these data suggest that targeting MTHFD2 activity is likely to influence multiple metabolic pathways in breast cancer and could be combined with a range of antimetabolite therapies.</description><identifier>ISSN: 1535-3893</identifier><identifier>EISSN: 1535-3907</identifier><identifier>DOI: 10.1021/acs.jproteome.6b00188</identifier><identifier>PMID: 27315223</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Aminohydrolases - deficiency ; Folic Acid - metabolism ; Gene Expression Regulation, Enzymologic ; Gene Knockdown Techniques ; Glycine - metabolism ; Glycolysis ; Humans ; MCF-7 Cells ; Metabolic Networks and Pathways ; Metabolome ; Methenyltetrahydrofolate Cyclohydrolase - deficiency ; Methylenetetrahydrofolate Dehydrogenase (NADP) - deficiency ; Multifunctional Enzymes - deficiency ; Neoplasm Proteins</subject><ispartof>Journal of proteome research, 2016-08, Vol.15 (8), p.2618-2625</ispartof><rights>Copyright © 2016 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a464t-9c11e703b251a1f9906a046a7de4697eb4eb3ee26acb5f5cde544853a3b4f67a3</citedby><cites>FETCH-LOGICAL-a464t-9c11e703b251a1f9906a046a7de4697eb4eb3ee26acb5f5cde544853a3b4f67a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.jproteome.6b00188$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.jproteome.6b00188$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27315223$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koufaris, Costas</creatorcontrib><creatorcontrib>Gallage, Suchira</creatorcontrib><creatorcontrib>Yang, Tianlai</creatorcontrib><creatorcontrib>Lau, Chung-Ho</creatorcontrib><creatorcontrib>Valbuena, Gabriel N</creatorcontrib><creatorcontrib>Keun, Hector C</creatorcontrib><title>Suppression of MTHFD2 in MCF‑7 Breast Cancer Cells Increases Glycolysis, Dependency on Exogenous Glycine, and Sensitivity to Folate Depletion</title><title>Journal of proteome research</title><addtitle>J. Proteome Res</addtitle><description>Methylenetetrahydrofolate dehydrogenase (NAD(P)+ dependent) 2, methenyltetrahydrofolate cyclohydrolase (MTHFD2) is a mitochondrial enzyme involved in folate metabolism. A number of recent studies have highlighted this enzyme as being highly expressed in many solid tumors, including breast cancer, and to be correlated with poor survival. However, the metabolic functions of MTHFD2 in cancer cells have not been well-defined. To investigate the function of MTHFD2 in breast cancer cells, we generated and characterized MCF-7 cells with stable suppression of MTHFD2 expression using a combination of cellular assays and metabolic profiling. Loss of MTHFD2 caused MCF7 cells to become glycine auxotrophs, that is, reliant on exogenous glycine, and more sensitive to exogenous folate depletion. Another prominent metabolic alteration observed as a consequence of MTHFD2 suppression was a more glycolytic phenotype, consistent with widespread modifications of cellular metabolism. Collectively, these data suggest that targeting MTHFD2 activity is likely to influence multiple metabolic pathways in breast cancer and could be combined with a range of antimetabolite therapies.</description><subject>Aminohydrolases - deficiency</subject><subject>Folic Acid - metabolism</subject><subject>Gene Expression Regulation, Enzymologic</subject><subject>Gene Knockdown Techniques</subject><subject>Glycine - metabolism</subject><subject>Glycolysis</subject><subject>Humans</subject><subject>MCF-7 Cells</subject><subject>Metabolic Networks and Pathways</subject><subject>Metabolome</subject><subject>Methenyltetrahydrofolate Cyclohydrolase - deficiency</subject><subject>Methylenetetrahydrofolate Dehydrogenase (NADP) - deficiency</subject><subject>Multifunctional Enzymes - deficiency</subject><subject>Neoplasm Proteins</subject><issn>1535-3893</issn><issn>1535-3907</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1OxCAUhYnR-P8IGpYunBFKoe1Sq6MmGhfquqH01mA6UIEau_MNjK_ok8g4o1tXEPKdwz33IHRAyZSShJ5I5afPvbMB7BymoiaE5vka2qac8QkrSLb-e88LtoV2vH-OCM8I20RbScYoTxK2jT7uh7534L22BtsW3z5czc4TrA2-LWdf758ZPnMgfcClNAocLqHrPL42avEKHl92o7Ld6LU_xufQg2nAqBFHs4s3-wTGDktGGzjG0jT4HozXQb_qMOJg8cx2MsBC2kGIM-yhjVZ2HvZX5y56nF08lFeTm7vL6_L0ZiJTkYZJoSiFmKVOOJW0LQoiJEmFzBpIRZFBnULNABIhVc1brhrgaZpzJlmdtiKTbBcdLX3jCl8G8KGaa69iOGkgzlzRnBSCiJyTiPIlqpz13kFb9U7PpRsrSqpFF1Xsovrrolp1EXWHqy-Geg7Nn-p3-RGgS-BHbwdnYuJ_TL8Bcx6cPg</recordid><startdate>20160805</startdate><enddate>20160805</enddate><creator>Koufaris, Costas</creator><creator>Gallage, Suchira</creator><creator>Yang, Tianlai</creator><creator>Lau, Chung-Ho</creator><creator>Valbuena, Gabriel N</creator><creator>Keun, Hector C</creator><general>American Chemical Society</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></search><sort><creationdate>20160805</creationdate><title>Suppression of MTHFD2 in MCF‑7 Breast Cancer Cells Increases Glycolysis, Dependency on Exogenous Glycine, and Sensitivity to Folate Depletion</title><author>Koufaris, Costas ; Gallage, Suchira ; Yang, Tianlai ; Lau, Chung-Ho ; Valbuena, Gabriel N ; Keun, Hector C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a464t-9c11e703b251a1f9906a046a7de4697eb4eb3ee26acb5f5cde544853a3b4f67a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Aminohydrolases - deficiency</topic><topic>Folic Acid - metabolism</topic><topic>Gene Expression Regulation, Enzymologic</topic><topic>Gene Knockdown Techniques</topic><topic>Glycine - metabolism</topic><topic>Glycolysis</topic><topic>Humans</topic><topic>MCF-7 Cells</topic><topic>Metabolic Networks and Pathways</topic><topic>Metabolome</topic><topic>Methenyltetrahydrofolate Cyclohydrolase - deficiency</topic><topic>Methylenetetrahydrofolate Dehydrogenase (NADP) - deficiency</topic><topic>Multifunctional Enzymes - deficiency</topic><topic>Neoplasm Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koufaris, Costas</creatorcontrib><creatorcontrib>Gallage, Suchira</creatorcontrib><creatorcontrib>Yang, Tianlai</creatorcontrib><creatorcontrib>Lau, Chung-Ho</creatorcontrib><creatorcontrib>Valbuena, Gabriel N</creatorcontrib><creatorcontrib>Keun, Hector C</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>Journal of proteome research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koufaris, Costas</au><au>Gallage, Suchira</au><au>Yang, Tianlai</au><au>Lau, Chung-Ho</au><au>Valbuena, Gabriel N</au><au>Keun, Hector C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Suppression of MTHFD2 in MCF‑7 Breast Cancer Cells Increases Glycolysis, Dependency on Exogenous Glycine, and Sensitivity to Folate Depletion</atitle><jtitle>Journal of proteome research</jtitle><addtitle>J. Proteome Res</addtitle><date>2016-08-05</date><risdate>2016</risdate><volume>15</volume><issue>8</issue><spage>2618</spage><epage>2625</epage><pages>2618-2625</pages><issn>1535-3893</issn><eissn>1535-3907</eissn><abstract>Methylenetetrahydrofolate dehydrogenase (NAD(P)+ dependent) 2, methenyltetrahydrofolate cyclohydrolase (MTHFD2) is a mitochondrial enzyme involved in folate metabolism. A number of recent studies have highlighted this enzyme as being highly expressed in many solid tumors, including breast cancer, and to be correlated with poor survival. However, the metabolic functions of MTHFD2 in cancer cells have not been well-defined. To investigate the function of MTHFD2 in breast cancer cells, we generated and characterized MCF-7 cells with stable suppression of MTHFD2 expression using a combination of cellular assays and metabolic profiling. Loss of MTHFD2 caused MCF7 cells to become glycine auxotrophs, that is, reliant on exogenous glycine, and more sensitive to exogenous folate depletion. Another prominent metabolic alteration observed as a consequence of MTHFD2 suppression was a more glycolytic phenotype, consistent with widespread modifications of cellular metabolism. Collectively, these data suggest that targeting MTHFD2 activity is likely to influence multiple metabolic pathways in breast cancer and could be combined with a range of antimetabolite therapies.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>27315223</pmid><doi>10.1021/acs.jproteome.6b00188</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aminohydrolases - deficiency Folic Acid - metabolism Gene Expression Regulation, Enzymologic Gene Knockdown Techniques Glycine - metabolism Glycolysis Humans MCF-7 Cells Metabolic Networks and Pathways Metabolome Methenyltetrahydrofolate Cyclohydrolase - deficiency Methylenetetrahydrofolate Dehydrogenase (NADP) - deficiency Multifunctional Enzymes - deficiency Neoplasm Proteins |
title | Suppression of MTHFD2 in MCF‑7 Breast Cancer Cells Increases Glycolysis, Dependency on Exogenous Glycine, and Sensitivity to Folate Depletion |
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