Metabolomics of the Tumor Microenvironment in Pediatric Acute Lymphoblastic Leukemia: e82859

The tumor microenvironment is emerging as an important therapeutic target. Most studies, however, are focused on the protein components, and relatively little is known of how the microenvironmental metabolome might influence tumor survival. In this study, we examined the metabolic profiles of paired...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:PloS one 2013-12, Vol.8 (12)
Hauptverfasser: Tiziani, Stefano, Kang, Yunyi, Harjanto, Ricky, Axelrod, Joshua, Piermarocchi, Carlo, Roberts, William, Paternostro, Giovanni
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 12
container_start_page
container_title PloS one
container_volume 8
creator Tiziani, Stefano
Kang, Yunyi
Harjanto, Ricky
Axelrod, Joshua
Piermarocchi, Carlo
Roberts, William
Paternostro, Giovanni
description The tumor microenvironment is emerging as an important therapeutic target. Most studies, however, are focused on the protein components, and relatively little is known of how the microenvironmental metabolome might influence tumor survival. In this study, we examined the metabolic profiles of paired bone marrow (BM) and peripheral blood (PB) samples from 10 children with acute lymphoblastic leukemia (ALL). BM and PB samples from the same patient were collected at the time of diagnosis and after 29 days of induction therapy, at which point all patients were in remission. We employed two analytical platforms, high-resolution magnetic resonance spectroscopy and gas chromatography-mass spectrometry, to identify and quantify 102 metabolites in the BM and PB. Standard ALL therapy, which includes l-asparaginase, completely removed circulating asparagine, but not glutamine. Statistical analyses of metabolite correlations and network reconstructions showed that the untreated BM microenvironment was characterized by a significant network-level signature: a cluster of highly correlated lipids and metabolites involved in lipid metabolism (p
doi_str_mv 10.1371/journal.pone.0082859
format Article
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_1492646464</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1492646464</sourcerecordid><originalsourceid>FETCH-proquest_miscellaneous_14926464643</originalsourceid><addsrcrecordid>eNqVjc1qAjEURkNBqFrfoIu7dOM0meh0xp2I0oVCFy4FiekVY5PcMT-Cb68tvoB8iwOHAx9j74IXQn6KjxPl4JUtWvJYcF6X9aR5YV3RyHJUlVy-sl6MJ84nsq6qLtuuMak9WXJGR6ADpCPCJjsKsDY6EPqLCeQd-gTGwzf-GJWC0TDTOSGsrq490t6qmO5uhfkXnVFTwP_fN9Y5KBtx8GCfDZeLzfxr1AY6Z4xp50zUaK3ySDnuxLgpq_Hf5BPpDXg9Tm4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1492646464</pqid></control><display><type>article</type><title>Metabolomics of the Tumor Microenvironment in Pediatric Acute Lymphoblastic Leukemia: e82859</title><source>DOAJ Directory of Open Access Journals</source><source>Public Library of Science (PLoS)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Tiziani, Stefano ; Kang, Yunyi ; Harjanto, Ricky ; Axelrod, Joshua ; Piermarocchi, Carlo ; Roberts, William ; Paternostro, Giovanni</creator><creatorcontrib>Tiziani, Stefano ; Kang, Yunyi ; Harjanto, Ricky ; Axelrod, Joshua ; Piermarocchi, Carlo ; Roberts, William ; Paternostro, Giovanni</creatorcontrib><description>The tumor microenvironment is emerging as an important therapeutic target. Most studies, however, are focused on the protein components, and relatively little is known of how the microenvironmental metabolome might influence tumor survival. In this study, we examined the metabolic profiles of paired bone marrow (BM) and peripheral blood (PB) samples from 10 children with acute lymphoblastic leukemia (ALL). BM and PB samples from the same patient were collected at the time of diagnosis and after 29 days of induction therapy, at which point all patients were in remission. We employed two analytical platforms, high-resolution magnetic resonance spectroscopy and gas chromatography-mass spectrometry, to identify and quantify 102 metabolites in the BM and PB. Standard ALL therapy, which includes l-asparaginase, completely removed circulating asparagine, but not glutamine. Statistical analyses of metabolite correlations and network reconstructions showed that the untreated BM microenvironment was characterized by a significant network-level signature: a cluster of highly correlated lipids and metabolites involved in lipid metabolism (p&lt;0.006). In contrast, the strongest correlations in the BM upon remission were observed among amino acid metabolites and derivatives (p&lt;9.210-10). This study provides evidence that metabolic characterization of the cancer niche could generate new hypotheses for the development of cancer therapies.</description><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0082859</identifier><language>eng</language><ispartof>PloS one, 2013-12, Vol.8 (12)</ispartof><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>314,777,781,861,27905,27906</link.rule.ids></links><search><creatorcontrib>Tiziani, Stefano</creatorcontrib><creatorcontrib>Kang, Yunyi</creatorcontrib><creatorcontrib>Harjanto, Ricky</creatorcontrib><creatorcontrib>Axelrod, Joshua</creatorcontrib><creatorcontrib>Piermarocchi, Carlo</creatorcontrib><creatorcontrib>Roberts, William</creatorcontrib><creatorcontrib>Paternostro, Giovanni</creatorcontrib><title>Metabolomics of the Tumor Microenvironment in Pediatric Acute Lymphoblastic Leukemia: e82859</title><title>PloS one</title><description>The tumor microenvironment is emerging as an important therapeutic target. Most studies, however, are focused on the protein components, and relatively little is known of how the microenvironmental metabolome might influence tumor survival. In this study, we examined the metabolic profiles of paired bone marrow (BM) and peripheral blood (PB) samples from 10 children with acute lymphoblastic leukemia (ALL). BM and PB samples from the same patient were collected at the time of diagnosis and after 29 days of induction therapy, at which point all patients were in remission. We employed two analytical platforms, high-resolution magnetic resonance spectroscopy and gas chromatography-mass spectrometry, to identify and quantify 102 metabolites in the BM and PB. Standard ALL therapy, which includes l-asparaginase, completely removed circulating asparagine, but not glutamine. Statistical analyses of metabolite correlations and network reconstructions showed that the untreated BM microenvironment was characterized by a significant network-level signature: a cluster of highly correlated lipids and metabolites involved in lipid metabolism (p&lt;0.006). In contrast, the strongest correlations in the BM upon remission were observed among amino acid metabolites and derivatives (p&lt;9.210-10). This study provides evidence that metabolic characterization of the cancer niche could generate new hypotheses for the development of cancer therapies.</description><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqVjc1qAjEURkNBqFrfoIu7dOM0meh0xp2I0oVCFy4FiekVY5PcMT-Cb68tvoB8iwOHAx9j74IXQn6KjxPl4JUtWvJYcF6X9aR5YV3RyHJUlVy-sl6MJ84nsq6qLtuuMak9WXJGR6ADpCPCJjsKsDY6EPqLCeQd-gTGwzf-GJWC0TDTOSGsrq490t6qmO5uhfkXnVFTwP_fN9Y5KBtx8GCfDZeLzfxr1AY6Z4xp50zUaK3ySDnuxLgpq_Hf5BPpDXg9Tm4</recordid><startdate>20131201</startdate><enddate>20131201</enddate><creator>Tiziani, Stefano</creator><creator>Kang, Yunyi</creator><creator>Harjanto, Ricky</creator><creator>Axelrod, Joshua</creator><creator>Piermarocchi, Carlo</creator><creator>Roberts, William</creator><creator>Paternostro, Giovanni</creator><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>20131201</creationdate><title>Metabolomics of the Tumor Microenvironment in Pediatric Acute Lymphoblastic Leukemia: e82859</title><author>Tiziani, Stefano ; Kang, Yunyi ; Harjanto, Ricky ; Axelrod, Joshua ; Piermarocchi, Carlo ; Roberts, William ; Paternostro, Giovanni</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_14926464643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tiziani, Stefano</creatorcontrib><creatorcontrib>Kang, Yunyi</creatorcontrib><creatorcontrib>Harjanto, Ricky</creatorcontrib><creatorcontrib>Axelrod, Joshua</creatorcontrib><creatorcontrib>Piermarocchi, Carlo</creatorcontrib><creatorcontrib>Roberts, William</creatorcontrib><creatorcontrib>Paternostro, Giovanni</creatorcontrib><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tiziani, Stefano</au><au>Kang, Yunyi</au><au>Harjanto, Ricky</au><au>Axelrod, Joshua</au><au>Piermarocchi, Carlo</au><au>Roberts, William</au><au>Paternostro, Giovanni</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolomics of the Tumor Microenvironment in Pediatric Acute Lymphoblastic Leukemia: e82859</atitle><jtitle>PloS one</jtitle><date>2013-12-01</date><risdate>2013</risdate><volume>8</volume><issue>12</issue><eissn>1932-6203</eissn><abstract>The tumor microenvironment is emerging as an important therapeutic target. Most studies, however, are focused on the protein components, and relatively little is known of how the microenvironmental metabolome might influence tumor survival. In this study, we examined the metabolic profiles of paired bone marrow (BM) and peripheral blood (PB) samples from 10 children with acute lymphoblastic leukemia (ALL). BM and PB samples from the same patient were collected at the time of diagnosis and after 29 days of induction therapy, at which point all patients were in remission. We employed two analytical platforms, high-resolution magnetic resonance spectroscopy and gas chromatography-mass spectrometry, to identify and quantify 102 metabolites in the BM and PB. Standard ALL therapy, which includes l-asparaginase, completely removed circulating asparagine, but not glutamine. Statistical analyses of metabolite correlations and network reconstructions showed that the untreated BM microenvironment was characterized by a significant network-level signature: a cluster of highly correlated lipids and metabolites involved in lipid metabolism (p&lt;0.006). In contrast, the strongest correlations in the BM upon remission were observed among amino acid metabolites and derivatives (p&lt;9.210-10). This study provides evidence that metabolic characterization of the cancer niche could generate new hypotheses for the development of cancer therapies.</abstract><doi>10.1371/journal.pone.0082859</doi></addata></record>
fulltext fulltext
identifier EISSN: 1932-6203
ispartof PloS one, 2013-12, Vol.8 (12)
issn 1932-6203
language eng
recordid cdi_proquest_miscellaneous_1492646464
source DOAJ Directory of Open Access Journals; Public Library of Science (PLoS); EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry
title Metabolomics of the Tumor Microenvironment in Pediatric Acute Lymphoblastic Leukemia: e82859
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T11%3A30%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Metabolomics%20of%20the%20Tumor%20Microenvironment%20in%20Pediatric%20Acute%20Lymphoblastic%20Leukemia:%20e82859&rft.jtitle=PloS%20one&rft.au=Tiziani,%20Stefano&rft.date=2013-12-01&rft.volume=8&rft.issue=12&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0082859&rft_dat=%3Cproquest%3E1492646464%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1492646464&rft_id=info:pmid/&rfr_iscdi=true