Detection of Tumor Messenger RNA in the Serum of Patients with Malignant Melanoma
Serum RNases are known to be elevated in patients with cancer. Consequently, it is not clear whether human mRNA with sufficient integrity as to permit reverse transcription-PCR (RT-PCR) amplification is detectable in serum. We examined serum from six patients with malignant melanoma for human tyrosi...
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Veröffentlicht in: | Clinical cancer research 1999-08, Vol.5 (8), p.1961-1965 |
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container_end_page | 1965 |
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container_issue | 8 |
container_start_page | 1961 |
container_title | Clinical cancer research |
container_volume | 5 |
creator | KOPRESKI, M. S BENKO, F. A KWAK, L. W GOCKE, C. D |
description | Serum RNases are known to be elevated in patients with cancer. Consequently, it is not clear whether human mRNA with sufficient
integrity as to permit reverse transcription-PCR (RT-PCR) amplification is detectable in serum. We examined serum from six
patients with malignant melanoma for human tyrosinase mRNA using RT-PCR. Serum from 20 normal volunteers served as controls.
Tyrosinase mRNA could be demonstrated in serum from four of the six melanoma patients with detection by gel electrophoresis
and confirmation by blotting amplified product to a tyrosinase-specific probe. The serum remained tyrosinase mRNA positive,
even if passed through a 0.45 μm filter prior to RNA extraction, indicating that the mRNA was extracellular at the time of
extraction. Tyrosinase mRNA could not be detected in any control serum (0 of 20 individuals). The presence and integrity of
amplifiable RNA was confirmed in all serum specimens (patients and controls) by RT-PCR amplification of c-abl mRNA. Amplifiable
RNA could be demonstrated regardless of whether serum was freshly drawn or stored frozen for several years. We conclude that
human mRNA can be extracted and amplified from serum. The ability to amplify tumor mRNA from serum may have important utility
in cancer diagnostics and monitoring. |
format | Article |
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integrity as to permit reverse transcription-PCR (RT-PCR) amplification is detectable in serum. We examined serum from six
patients with malignant melanoma for human tyrosinase mRNA using RT-PCR. Serum from 20 normal volunteers served as controls.
Tyrosinase mRNA could be demonstrated in serum from four of the six melanoma patients with detection by gel electrophoresis
and confirmation by blotting amplified product to a tyrosinase-specific probe. The serum remained tyrosinase mRNA positive,
even if passed through a 0.45 μm filter prior to RNA extraction, indicating that the mRNA was extracellular at the time of
extraction. Tyrosinase mRNA could not be detected in any control serum (0 of 20 individuals). The presence and integrity of
amplifiable RNA was confirmed in all serum specimens (patients and controls) by RT-PCR amplification of c-abl mRNA. Amplifiable
RNA could be demonstrated regardless of whether serum was freshly drawn or stored frozen for several years. We conclude that
human mRNA can be extracted and amplified from serum. The ability to amplify tumor mRNA from serum may have important utility
in cancer diagnostics and monitoring.</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>PMID: 10473072</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Biological and medical sciences ; Blotting, Southern ; Dermatology ; Electrophoresis, Agar Gel ; Freezing ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Medical sciences ; Melanoma - blood ; Melanoma - enzymology ; Miscellaneous. Technology ; Monophenol Monooxygenase - blood ; Monophenol Monooxygenase - genetics ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Predictive Value of Tests ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - blood ; RNA, Messenger - chemistry ; RNA, Neoplasm - blood ; RNA, Neoplasm - chemistry ; Sensitivity and Specificity ; Tumors of the skin and soft tissue. Premalignant lesions</subject><ispartof>Clinical cancer research, 1999-08, Vol.5 (8), p.1961-1965</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1954501$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10473072$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KOPRESKI, M. S</creatorcontrib><creatorcontrib>BENKO, F. A</creatorcontrib><creatorcontrib>KWAK, L. W</creatorcontrib><creatorcontrib>GOCKE, C. D</creatorcontrib><title>Detection of Tumor Messenger RNA in the Serum of Patients with Malignant Melanoma</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>Serum RNases are known to be elevated in patients with cancer. Consequently, it is not clear whether human mRNA with sufficient
integrity as to permit reverse transcription-PCR (RT-PCR) amplification is detectable in serum. We examined serum from six
patients with malignant melanoma for human tyrosinase mRNA using RT-PCR. Serum from 20 normal volunteers served as controls.
Tyrosinase mRNA could be demonstrated in serum from four of the six melanoma patients with detection by gel electrophoresis
and confirmation by blotting amplified product to a tyrosinase-specific probe. The serum remained tyrosinase mRNA positive,
even if passed through a 0.45 μm filter prior to RNA extraction, indicating that the mRNA was extracellular at the time of
extraction. Tyrosinase mRNA could not be detected in any control serum (0 of 20 individuals). The presence and integrity of
amplifiable RNA was confirmed in all serum specimens (patients and controls) by RT-PCR amplification of c-abl mRNA. Amplifiable
RNA could be demonstrated regardless of whether serum was freshly drawn or stored frozen for several years. We conclude that
human mRNA can be extracted and amplified from serum. The ability to amplify tumor mRNA from serum may have important utility
in cancer diagnostics and monitoring.</description><subject>Biological and medical sciences</subject><subject>Blotting, Southern</subject><subject>Dermatology</subject><subject>Electrophoresis, Agar Gel</subject><subject>Freezing</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Medical sciences</subject><subject>Melanoma - blood</subject><subject>Melanoma - enzymology</subject><subject>Miscellaneous. Technology</subject><subject>Monophenol Monooxygenase - blood</subject><subject>Monophenol Monooxygenase - genetics</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Predictive Value of Tests</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - blood</subject><subject>RNA, Messenger - chemistry</subject><subject>RNA, Neoplasm - blood</subject><subject>RNA, Neoplasm - chemistry</subject><subject>Sensitivity and Specificity</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0EtPwzAMAOAKgdgY_AWUA4JTpSRtXsdpPKWN5zhXWeauQW06klQT_54ghrjYlvzZsnyQjQljIi8oZ4epxkLmuCzoKDsJ4QNjUhJcHmejFEWBBR1nL9cQwUTbO9TXaDl0vUcLCAHcBjx6fZwi61BsAL2BH7of86yjBRcD2tnYoIVu7cZpF9NUq13f6dPsqNZtgLN9nmTvtzfL2X0-f7p7mE3neUO5jLmSUjOy4lTUgirCDNcKcwVFKYWoyZpTVXBBzUpqyUsgOLUZZwKkoXWteDHJLn_3bn3_OUCIVWeDgTZdAf0QKoExloqzBM_3cFh1sK623nbaf1V_T0jgYg90MLqtvXbGhn-nWMkwSezqlzV20-ysh8okCN5DAO1NU7FKJsxJ8Q3C8HG8</recordid><startdate>19990801</startdate><enddate>19990801</enddate><creator>KOPRESKI, M. S</creator><creator>BENKO, F. A</creator><creator>KWAK, L. W</creator><creator>GOCKE, C. D</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19990801</creationdate><title>Detection of Tumor Messenger RNA in the Serum of Patients with Malignant Melanoma</title><author>KOPRESKI, M. S ; BENKO, F. A ; KWAK, L. W ; GOCKE, C. D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h268t-988a51b627f72915c6a9069e34877f1d6293672cb8a864e10a905657e8c2ff963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Biological and medical sciences</topic><topic>Blotting, Southern</topic><topic>Dermatology</topic><topic>Electrophoresis, Agar Gel</topic><topic>Freezing</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Medical sciences</topic><topic>Melanoma - blood</topic><topic>Melanoma - enzymology</topic><topic>Miscellaneous. Technology</topic><topic>Monophenol Monooxygenase - blood</topic><topic>Monophenol Monooxygenase - genetics</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Predictive Value of Tests</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - blood</topic><topic>RNA, Messenger - chemistry</topic><topic>RNA, Neoplasm - blood</topic><topic>RNA, Neoplasm - chemistry</topic><topic>Sensitivity and Specificity</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KOPRESKI, M. S</creatorcontrib><creatorcontrib>BENKO, F. A</creatorcontrib><creatorcontrib>KWAK, L. W</creatorcontrib><creatorcontrib>GOCKE, C. D</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KOPRESKI, M. S</au><au>BENKO, F. A</au><au>KWAK, L. W</au><au>GOCKE, C. D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of Tumor Messenger RNA in the Serum of Patients with Malignant Melanoma</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>1999-08-01</date><risdate>1999</risdate><volume>5</volume><issue>8</issue><spage>1961</spage><epage>1965</epage><pages>1961-1965</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><abstract>Serum RNases are known to be elevated in patients with cancer. Consequently, it is not clear whether human mRNA with sufficient
integrity as to permit reverse transcription-PCR (RT-PCR) amplification is detectable in serum. We examined serum from six
patients with malignant melanoma for human tyrosinase mRNA using RT-PCR. Serum from 20 normal volunteers served as controls.
Tyrosinase mRNA could be demonstrated in serum from four of the six melanoma patients with detection by gel electrophoresis
and confirmation by blotting amplified product to a tyrosinase-specific probe. The serum remained tyrosinase mRNA positive,
even if passed through a 0.45 μm filter prior to RNA extraction, indicating that the mRNA was extracellular at the time of
extraction. Tyrosinase mRNA could not be detected in any control serum (0 of 20 individuals). The presence and integrity of
amplifiable RNA was confirmed in all serum specimens (patients and controls) by RT-PCR amplification of c-abl mRNA. Amplifiable
RNA could be demonstrated regardless of whether serum was freshly drawn or stored frozen for several years. We conclude that
human mRNA can be extracted and amplified from serum. The ability to amplify tumor mRNA from serum may have important utility
in cancer diagnostics and monitoring.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>10473072</pmid><tpages>5</tpages></addata></record> |
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source | MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Biological and medical sciences Blotting, Southern Dermatology Electrophoresis, Agar Gel Freezing Humans Investigative techniques, diagnostic techniques (general aspects) Medical sciences Melanoma - blood Melanoma - enzymology Miscellaneous. Technology Monophenol Monooxygenase - blood Monophenol Monooxygenase - genetics Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Predictive Value of Tests Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - blood RNA, Messenger - chemistry RNA, Neoplasm - blood RNA, Neoplasm - chemistry Sensitivity and Specificity Tumors of the skin and soft tissue. Premalignant lesions |
title | Detection of Tumor Messenger RNA in the Serum of Patients with Malignant Melanoma |
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