(1)H NMR metabolomics analysis of renal cell carcinoma cells: Effect of VHL inactivation on metabolism
Von Hippel-Lindau (VHL) is an onco-suppressor involved in oxygen and energy-dependent promotion of protein ubiquitination and proteosomal degradation. Loss of function mutations of VHL (VHL-cells) result in organ specific cancers with the best studied example in renal cell carcinomas. VHL has a well...
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Veröffentlicht in: | International journal of cancer 2016-05, Vol.138 (10), p.2439-2449 |
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creator | Cuperlovic-Culf, Miroslava Cormier, Kevin Touaibia, Mohamed Reyjal, Julie Robichaud, Sarah Belbraouet, Mehdi Turcotte, Sandra |
description | Von Hippel-Lindau (VHL) is an onco-suppressor involved in oxygen and energy-dependent promotion of protein ubiquitination and proteosomal degradation. Loss of function mutations of VHL (VHL-cells) result in organ specific cancers with the best studied example in renal cell carcinomas. VHL has a well-established role in deactivation of hypoxia-inducible factor (HIF-1) and in regulation of PI3K/AKT/mTOR activity. Cell culture metabolomics analysis was utilized to determined effect of VHL and HIF-1α or HIF-2α on metabolism of renal cell carcinomas (RCC). RCC cells were stably transfected with VHL or shRNA designed to silence HIF-1α or HIF-2α genes. Obtained metabolic data was analysed qualitatively, searching for overall effects on metabolism as well as quantitatively, using methods developed in our group in order to determine specific metabolic changes. Analysis of the effect of VHL and HIF silencing on cellular metabolic footprints and fingerprints provided information about the metabolic pathways affected by VHL through HIF function as well as independently of HIF. Through correlation network analysis as well as statistical analysis of significant metabolic changes we have determined effects of VHL and HIF on energy production, amino acid metabolism, choline metabolism as well as cell regulation and signaling. VHL was shown to influence cellular metabolism through its effect on HIF proteins as well as by affecting activity of other factors. |
doi_str_mv | 10.1002/ijc.29947 |
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Loss of function mutations of VHL (VHL-cells) result in organ specific cancers with the best studied example in renal cell carcinomas. VHL has a well-established role in deactivation of hypoxia-inducible factor (HIF-1) and in regulation of PI3K/AKT/mTOR activity. Cell culture metabolomics analysis was utilized to determined effect of VHL and HIF-1α or HIF-2α on metabolism of renal cell carcinomas (RCC). RCC cells were stably transfected with VHL or shRNA designed to silence HIF-1α or HIF-2α genes. Obtained metabolic data was analysed qualitatively, searching for overall effects on metabolism as well as quantitatively, using methods developed in our group in order to determine specific metabolic changes. Analysis of the effect of VHL and HIF silencing on cellular metabolic footprints and fingerprints provided information about the metabolic pathways affected by VHL through HIF function as well as independently of HIF. Through correlation network analysis as well as statistical analysis of significant metabolic changes we have determined effects of VHL and HIF on energy production, amino acid metabolism, choline metabolism as well as cell regulation and signaling. VHL was shown to influence cellular metabolism through its effect on HIF proteins as well as by affecting activity of other factors.</description><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.29947</identifier><identifier>PMID: 26620126</identifier><language>eng</language><publisher>United States</publisher><subject>Basic Helix-Loop-Helix Transcription Factors - genetics ; Basic Helix-Loop-Helix Transcription Factors - metabolism ; Carcinoma, Renal Cell - genetics ; Carcinoma, Renal Cell - metabolism ; Cell Line, Tumor ; Cluster Analysis ; Gene Knockdown Techniques ; Gene Silencing ; Humans ; Hypoxia-Inducible Factor 1, alpha Subunit - genetics ; Hypoxia-Inducible Factor 1, alpha Subunit - metabolism ; Kidney Neoplasms - metabolism ; Metabolome ; Metabolomics - methods ; Mutation ; Proton Magnetic Resonance Spectroscopy - methods ; Von Hippel-Lindau Tumor Suppressor Protein - genetics ; Von Hippel-Lindau Tumor Suppressor Protein - metabolism</subject><ispartof>International journal of cancer, 2016-05, Vol.138 (10), p.2439-2449</ispartof><rights>2015 UICC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26620126$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cuperlovic-Culf, Miroslava</creatorcontrib><creatorcontrib>Cormier, Kevin</creatorcontrib><creatorcontrib>Touaibia, Mohamed</creatorcontrib><creatorcontrib>Reyjal, Julie</creatorcontrib><creatorcontrib>Robichaud, Sarah</creatorcontrib><creatorcontrib>Belbraouet, Mehdi</creatorcontrib><creatorcontrib>Turcotte, Sandra</creatorcontrib><title>(1)H NMR metabolomics analysis of renal cell carcinoma cells: Effect of VHL inactivation on metabolism</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>Von Hippel-Lindau (VHL) is an onco-suppressor involved in oxygen and energy-dependent promotion of protein ubiquitination and proteosomal degradation. Loss of function mutations of VHL (VHL-cells) result in organ specific cancers with the best studied example in renal cell carcinomas. VHL has a well-established role in deactivation of hypoxia-inducible factor (HIF-1) and in regulation of PI3K/AKT/mTOR activity. Cell culture metabolomics analysis was utilized to determined effect of VHL and HIF-1α or HIF-2α on metabolism of renal cell carcinomas (RCC). RCC cells were stably transfected with VHL or shRNA designed to silence HIF-1α or HIF-2α genes. Obtained metabolic data was analysed qualitatively, searching for overall effects on metabolism as well as quantitatively, using methods developed in our group in order to determine specific metabolic changes. Analysis of the effect of VHL and HIF silencing on cellular metabolic footprints and fingerprints provided information about the metabolic pathways affected by VHL through HIF function as well as independently of HIF. Through correlation network analysis as well as statistical analysis of significant metabolic changes we have determined effects of VHL and HIF on energy production, amino acid metabolism, choline metabolism as well as cell regulation and signaling. VHL was shown to influence cellular metabolism through its effect on HIF proteins as well as by affecting activity of other factors.</description><subject>Basic Helix-Loop-Helix Transcription Factors - genetics</subject><subject>Basic Helix-Loop-Helix Transcription Factors - metabolism</subject><subject>Carcinoma, Renal Cell - genetics</subject><subject>Carcinoma, Renal Cell - metabolism</subject><subject>Cell Line, Tumor</subject><subject>Cluster Analysis</subject><subject>Gene Knockdown Techniques</subject><subject>Gene Silencing</subject><subject>Humans</subject><subject>Hypoxia-Inducible Factor 1, alpha Subunit - genetics</subject><subject>Hypoxia-Inducible Factor 1, alpha Subunit - metabolism</subject><subject>Kidney Neoplasms - metabolism</subject><subject>Metabolome</subject><subject>Metabolomics - methods</subject><subject>Mutation</subject><subject>Proton Magnetic Resonance Spectroscopy - methods</subject><subject>Von Hippel-Lindau Tumor Suppressor Protein - genetics</subject><subject>Von Hippel-Lindau Tumor Suppressor Protein - metabolism</subject><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kE9LAzEQxYMgtlYPfgHJsR62zuTPxngTqVaoCqJelzSbQMpmUzdbod_erVYYZnjMj8ebIeQCYYYA7Dqs7YxpLdQRGSNoVQBDOSKnOa8BECWIEzJiZckAWTkmfopXC_ry_Eaj680qNSkGm6lpTbPLIdPkaecGQa1rhmY6G9oUza_Mt3TuvbP9nvpcLGloje3Dt-lDaulQB8uQ4xk59qbJ7vwwJ-TjYf5-vyiWr49P93fLYoO67AuGGmpvjIAbqS1jHJ1joBQ4K522Rgql0aMflkoIWavacMmHaznIFVOCT8j0z3fTpa-ty30VQ95nNa1L21yhUqhYKfgevTyg21V0dbXpQjTdrvr_Df8B4Bthgg</recordid><startdate>20160515</startdate><enddate>20160515</enddate><creator>Cuperlovic-Culf, Miroslava</creator><creator>Cormier, Kevin</creator><creator>Touaibia, Mohamed</creator><creator>Reyjal, Julie</creator><creator>Robichaud, Sarah</creator><creator>Belbraouet, Mehdi</creator><creator>Turcotte, Sandra</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20160515</creationdate><title>(1)H NMR metabolomics analysis of renal cell carcinoma cells: Effect of VHL inactivation on metabolism</title><author>Cuperlovic-Culf, Miroslava ; 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Loss of function mutations of VHL (VHL-cells) result in organ specific cancers with the best studied example in renal cell carcinomas. VHL has a well-established role in deactivation of hypoxia-inducible factor (HIF-1) and in regulation of PI3K/AKT/mTOR activity. Cell culture metabolomics analysis was utilized to determined effect of VHL and HIF-1α or HIF-2α on metabolism of renal cell carcinomas (RCC). RCC cells were stably transfected with VHL or shRNA designed to silence HIF-1α or HIF-2α genes. Obtained metabolic data was analysed qualitatively, searching for overall effects on metabolism as well as quantitatively, using methods developed in our group in order to determine specific metabolic changes. Analysis of the effect of VHL and HIF silencing on cellular metabolic footprints and fingerprints provided information about the metabolic pathways affected by VHL through HIF function as well as independently of HIF. Through correlation network analysis as well as statistical analysis of significant metabolic changes we have determined effects of VHL and HIF on energy production, amino acid metabolism, choline metabolism as well as cell regulation and signaling. VHL was shown to influence cellular metabolism through its effect on HIF proteins as well as by affecting activity of other factors.</abstract><cop>United States</cop><pmid>26620126</pmid><doi>10.1002/ijc.29947</doi><tpages>11</tpages></addata></record> |
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subjects | Basic Helix-Loop-Helix Transcription Factors - genetics Basic Helix-Loop-Helix Transcription Factors - metabolism Carcinoma, Renal Cell - genetics Carcinoma, Renal Cell - metabolism Cell Line, Tumor Cluster Analysis Gene Knockdown Techniques Gene Silencing Humans Hypoxia-Inducible Factor 1, alpha Subunit - genetics Hypoxia-Inducible Factor 1, alpha Subunit - metabolism Kidney Neoplasms - metabolism Metabolome Metabolomics - methods Mutation Proton Magnetic Resonance Spectroscopy - methods Von Hippel-Lindau Tumor Suppressor Protein - genetics Von Hippel-Lindau Tumor Suppressor Protein - metabolism |
title | (1)H NMR metabolomics analysis of renal cell carcinoma cells: Effect of VHL inactivation on metabolism |
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