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
Hauptverfasser: KOPRESKI, M. S, BENKO, F. A, KWAK, L. W, GOCKE, C. D
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container_end_page 1965
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.
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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. 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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. 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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. 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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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