Biochip array technology and evaluation of serum levels of multiple cytokines and adhesion molecules in patients with newly diagnosed acute myeloid leukemia

Evaluation of serum levels of 17 cytokines and 5 adhesion molecules in patients with newly diagnosed acute myeloid leukemia (AML) and in healthy subjects using biochip array technology. A total of 15 AML patients and 15 healthy subjects (blood donors) were studied. Serum samples were analyzed by bio...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Experimental oncology 2014-03, Vol.36 (1), p.50-51
Hauptverfasser: Horacek, J M, Kupsa, T, Vasatova, M, Jebavy, L, Zak, P
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 51
container_issue 1
container_start_page 50
container_title Experimental oncology
container_volume 36
creator Horacek, J M
Kupsa, T
Vasatova, M
Jebavy, L
Zak, P
description Evaluation of serum levels of 17 cytokines and 5 adhesion molecules in patients with newly diagnosed acute myeloid leukemia (AML) and in healthy subjects using biochip array technology. A total of 15 AML patients and 15 healthy subjects (blood donors) were studied. Serum samples were analyzed by biochip based immunoassays on the Evidence Investigator analyzer. This approach allows multi-analytical determination from a single sample. T-tests were used for statistical analysis. In newly diagnosed AML patients, we found significant increase (p < 0.01) in serum VCAM-1, ICAM-1, E-selectin, L-selectin, and significant increase (p < 0.05) in serum IL-6, IL-8. No significant differences were found in the levels of other evaluated cytokines and adhesion molecules. Our results indicate that serum levels of specific cytokines and adhesion molecules (VCAM-1, ICAM-1, E-selectin, L-selectin, IL-6, IL-8) are significantly altered in patients with newly diagnosed AML, showing activity of the disease. Whether these alterations could serve as a prognostic marker for AML is not known. Further studies will be needed to define the potential role of these and additional markers in the risk stratification of AML.
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_1512559759</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1512559759</sourcerecordid><originalsourceid>FETCH-LOGICAL-p126t-e778a29a0ce8f46f7cc1a4af92efa3427a9c79291b1aba219f31fe26b1b1dff93</originalsourceid><addsrcrecordid>eNo1kM1OwzAQhHMA0VJ4BeQjl0i1kzjxESr-pEpc4BxtnHVj6tghtlvlXXhYUn5Oox3NNyPtWbKkFWWpYFwskkvvP9ZrXgieXyQLlnNBWcWXyde9drLTA4FxhIkElJ11xu0mArYleAATIWhniVPE4xh7YvCAxp_uPpqgB4NETsHttUX_A0HboT8hvTMoo5ltbckw16ANnhx16IjFo5lIq2FnnceZkTEg6Sc0TrfzRNxjr-EqOVdgPF7_6Sp5f3x42zyn29enl83dNh0o4yHFsqyACVhLrFTOVSklhRyUYKggy1kJQpaCCdpQaIBRoTKqkPFmNlqlRLZKbn97h9F9RvSh7rWXaAxYdNHXtKCsKERZnKI3f9HY9NjWw6h7GKf6_6PZN1vGdo0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1512559759</pqid></control><display><type>article</type><title>Biochip array technology and evaluation of serum levels of multiple cytokines and adhesion molecules in patients with newly diagnosed acute myeloid leukemia</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Horacek, J M ; Kupsa, T ; Vasatova, M ; Jebavy, L ; Zak, P</creator><creatorcontrib>Horacek, J M ; Kupsa, T ; Vasatova, M ; Jebavy, L ; Zak, P</creatorcontrib><description>Evaluation of serum levels of 17 cytokines and 5 adhesion molecules in patients with newly diagnosed acute myeloid leukemia (AML) and in healthy subjects using biochip array technology. A total of 15 AML patients and 15 healthy subjects (blood donors) were studied. Serum samples were analyzed by biochip based immunoassays on the Evidence Investigator analyzer. This approach allows multi-analytical determination from a single sample. T-tests were used for statistical analysis. In newly diagnosed AML patients, we found significant increase (p &lt; 0.01) in serum VCAM-1, ICAM-1, E-selectin, L-selectin, and significant increase (p &lt; 0.05) in serum IL-6, IL-8. No significant differences were found in the levels of other evaluated cytokines and adhesion molecules. Our results indicate that serum levels of specific cytokines and adhesion molecules (VCAM-1, ICAM-1, E-selectin, L-selectin, IL-6, IL-8) are significantly altered in patients with newly diagnosed AML, showing activity of the disease. Whether these alterations could serve as a prognostic marker for AML is not known. Further studies will be needed to define the potential role of these and additional markers in the risk stratification of AML.</description><identifier>ISSN: 1812-9269</identifier><identifier>PMID: 24691286</identifier><language>eng</language><publisher>Ukraine</publisher><subject>Adult ; Biomarkers, Tumor - blood ; Cell Adhesion Molecules - blood ; Cytokines - blood ; E-Selectin - blood ; Female ; Humans ; Intercellular Adhesion Molecule-1 - blood ; Interleukin-6 - blood ; Interleukin-8 - blood ; L-Selectin - blood ; Leukemia, Myeloid, Acute - blood ; Leukemia, Myeloid, Acute - genetics ; Leukemia, Myeloid, Acute - pathology ; Male ; Middle Aged ; Protein Array Analysis - methods ; Vascular Cell Adhesion Molecule-1 - blood</subject><ispartof>Experimental oncology, 2014-03, Vol.36 (1), p.50-51</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24691286$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Horacek, J M</creatorcontrib><creatorcontrib>Kupsa, T</creatorcontrib><creatorcontrib>Vasatova, M</creatorcontrib><creatorcontrib>Jebavy, L</creatorcontrib><creatorcontrib>Zak, P</creatorcontrib><title>Biochip array technology and evaluation of serum levels of multiple cytokines and adhesion molecules in patients with newly diagnosed acute myeloid leukemia</title><title>Experimental oncology</title><addtitle>Exp Oncol</addtitle><description>Evaluation of serum levels of 17 cytokines and 5 adhesion molecules in patients with newly diagnosed acute myeloid leukemia (AML) and in healthy subjects using biochip array technology. A total of 15 AML patients and 15 healthy subjects (blood donors) were studied. Serum samples were analyzed by biochip based immunoassays on the Evidence Investigator analyzer. This approach allows multi-analytical determination from a single sample. T-tests were used for statistical analysis. In newly diagnosed AML patients, we found significant increase (p &lt; 0.01) in serum VCAM-1, ICAM-1, E-selectin, L-selectin, and significant increase (p &lt; 0.05) in serum IL-6, IL-8. No significant differences were found in the levels of other evaluated cytokines and adhesion molecules. Our results indicate that serum levels of specific cytokines and adhesion molecules (VCAM-1, ICAM-1, E-selectin, L-selectin, IL-6, IL-8) are significantly altered in patients with newly diagnosed AML, showing activity of the disease. Whether these alterations could serve as a prognostic marker for AML is not known. Further studies will be needed to define the potential role of these and additional markers in the risk stratification of AML.</description><subject>Adult</subject><subject>Biomarkers, Tumor - blood</subject><subject>Cell Adhesion Molecules - blood</subject><subject>Cytokines - blood</subject><subject>E-Selectin - blood</subject><subject>Female</subject><subject>Humans</subject><subject>Intercellular Adhesion Molecule-1 - blood</subject><subject>Interleukin-6 - blood</subject><subject>Interleukin-8 - blood</subject><subject>L-Selectin - blood</subject><subject>Leukemia, Myeloid, Acute - blood</subject><subject>Leukemia, Myeloid, Acute - genetics</subject><subject>Leukemia, Myeloid, Acute - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Protein Array Analysis - methods</subject><subject>Vascular Cell Adhesion Molecule-1 - blood</subject><issn>1812-9269</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kM1OwzAQhHMA0VJ4BeQjl0i1kzjxESr-pEpc4BxtnHVj6tghtlvlXXhYUn5Oox3NNyPtWbKkFWWpYFwskkvvP9ZrXgieXyQLlnNBWcWXyde9drLTA4FxhIkElJ11xu0mArYleAATIWhniVPE4xh7YvCAxp_uPpqgB4NETsHttUX_A0HboT8hvTMoo5ltbckw16ANnhx16IjFo5lIq2FnnceZkTEg6Sc0TrfzRNxjr-EqOVdgPF7_6Sp5f3x42zyn29enl83dNh0o4yHFsqyACVhLrFTOVSklhRyUYKggy1kJQpaCCdpQaIBRoTKqkPFmNlqlRLZKbn97h9F9RvSh7rWXaAxYdNHXtKCsKERZnKI3f9HY9NjWw6h7GKf6_6PZN1vGdo0</recordid><startdate>201403</startdate><enddate>201403</enddate><creator>Horacek, J M</creator><creator>Kupsa, T</creator><creator>Vasatova, M</creator><creator>Jebavy, L</creator><creator>Zak, P</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>201403</creationdate><title>Biochip array technology and evaluation of serum levels of multiple cytokines and adhesion molecules in patients with newly diagnosed acute myeloid leukemia</title><author>Horacek, J M ; Kupsa, T ; Vasatova, M ; Jebavy, L ; Zak, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p126t-e778a29a0ce8f46f7cc1a4af92efa3427a9c79291b1aba219f31fe26b1b1dff93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Biomarkers, Tumor - blood</topic><topic>Cell Adhesion Molecules - blood</topic><topic>Cytokines - blood</topic><topic>E-Selectin - blood</topic><topic>Female</topic><topic>Humans</topic><topic>Intercellular Adhesion Molecule-1 - blood</topic><topic>Interleukin-6 - blood</topic><topic>Interleukin-8 - blood</topic><topic>L-Selectin - blood</topic><topic>Leukemia, Myeloid, Acute - blood</topic><topic>Leukemia, Myeloid, Acute - genetics</topic><topic>Leukemia, Myeloid, Acute - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Protein Array Analysis - methods</topic><topic>Vascular Cell Adhesion Molecule-1 - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Horacek, J M</creatorcontrib><creatorcontrib>Kupsa, T</creatorcontrib><creatorcontrib>Vasatova, M</creatorcontrib><creatorcontrib>Jebavy, L</creatorcontrib><creatorcontrib>Zak, P</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Horacek, J M</au><au>Kupsa, T</au><au>Vasatova, M</au><au>Jebavy, L</au><au>Zak, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biochip array technology and evaluation of serum levels of multiple cytokines and adhesion molecules in patients with newly diagnosed acute myeloid leukemia</atitle><jtitle>Experimental oncology</jtitle><addtitle>Exp Oncol</addtitle><date>2014-03</date><risdate>2014</risdate><volume>36</volume><issue>1</issue><spage>50</spage><epage>51</epage><pages>50-51</pages><issn>1812-9269</issn><abstract>Evaluation of serum levels of 17 cytokines and 5 adhesion molecules in patients with newly diagnosed acute myeloid leukemia (AML) and in healthy subjects using biochip array technology. A total of 15 AML patients and 15 healthy subjects (blood donors) were studied. Serum samples were analyzed by biochip based immunoassays on the Evidence Investigator analyzer. This approach allows multi-analytical determination from a single sample. T-tests were used for statistical analysis. In newly diagnosed AML patients, we found significant increase (p &lt; 0.01) in serum VCAM-1, ICAM-1, E-selectin, L-selectin, and significant increase (p &lt; 0.05) in serum IL-6, IL-8. No significant differences were found in the levels of other evaluated cytokines and adhesion molecules. Our results indicate that serum levels of specific cytokines and adhesion molecules (VCAM-1, ICAM-1, E-selectin, L-selectin, IL-6, IL-8) are significantly altered in patients with newly diagnosed AML, showing activity of the disease. Whether these alterations could serve as a prognostic marker for AML is not known. Further studies will be needed to define the potential role of these and additional markers in the risk stratification of AML.</abstract><cop>Ukraine</cop><pmid>24691286</pmid><tpages>2</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1812-9269
ispartof Experimental oncology, 2014-03, Vol.36 (1), p.50-51
issn 1812-9269
language eng
recordid cdi_proquest_miscellaneous_1512559759
source MEDLINE; Alma/SFX Local Collection
subjects Adult
Biomarkers, Tumor - blood
Cell Adhesion Molecules - blood
Cytokines - blood
E-Selectin - blood
Female
Humans
Intercellular Adhesion Molecule-1 - blood
Interleukin-6 - blood
Interleukin-8 - blood
L-Selectin - blood
Leukemia, Myeloid, Acute - blood
Leukemia, Myeloid, Acute - genetics
Leukemia, Myeloid, Acute - pathology
Male
Middle Aged
Protein Array Analysis - methods
Vascular Cell Adhesion Molecule-1 - blood
title Biochip array technology and evaluation of serum levels of multiple cytokines and adhesion molecules in patients with newly diagnosed acute myeloid leukemia
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T18%3A11%3A52IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Biochip%20array%20technology%20and%20evaluation%20of%20serum%20levels%20of%20multiple%20cytokines%20and%20adhesion%20molecules%20in%20patients%20with%20newly%20diagnosed%20acute%20myeloid%20leukemia&rft.jtitle=Experimental%20oncology&rft.au=Horacek,%20J%20M&rft.date=2014-03&rft.volume=36&rft.issue=1&rft.spage=50&rft.epage=51&rft.pages=50-51&rft.issn=1812-9269&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E1512559759%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1512559759&rft_id=info:pmid/24691286&rfr_iscdi=true