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...
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Veröffentlicht in: | Experimental oncology 2014-03, Vol.36 (1), p.50-51 |
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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. |
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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.</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 < 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.</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 < 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.</abstract><cop>Ukraine</cop><pmid>24691286</pmid><tpages>2</tpages></addata></record> |
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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 |
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