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Detection of mutant K-ras DNA in plasma or serum of patients with colorectal cancer.
Increased understanding of the molecular basis of colorectal cancer and recognition that extracellular DNA circulates in the plasma and serum of cancer patients enables new approaches to detection and monitoring. We used a polymerase chain reaction (PCR) assay to demonstrate mutant K-ras DNA in the...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1997
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2228153/ https://www.ncbi.nlm.nih.gov/pubmed/9374374 |
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author | Kopreski, M. S. Benko, F. A. Kwee, C. Leitzel, K. E. Eskander, E. Lipton, A. Gocke, C. D. |
author_facet | Kopreski, M. S. Benko, F. A. Kwee, C. Leitzel, K. E. Eskander, E. Lipton, A. Gocke, C. D. |
author_sort | Kopreski, M. S. |
collection | PubMed |
description | Increased understanding of the molecular basis of colorectal cancer and recognition that extracellular DNA circulates in the plasma and serum of cancer patients enables new approaches to detection and monitoring. We used a polymerase chain reaction (PCR) assay to demonstrate mutant K-ras DNA in the plasma or serum of patients with colorectal cancer. Plasma or serum was fractionated from the blood of 31 patients with metastatic or unresected colorectal cancer and from 28 normal volunteers. DNA was extracted using either a sodium chloride or a gelatin precipitation method and then amplified in a two-stage PCR assay using selective restriction enzyme digestion to enrich for mutant K-ras DNA. Mutant K-ras DNA was detected in the plasma or serum of 12 (39%) patients, all confirmed by sequencing, but was not detected in any of the normal volunteers. K-ras mutations were detected in plasma or serum regardless of sex, primary tumour location, principal site of metastasis or proximity of chemotherapy and surgery to blood sampling. Tumour specimens available for 19 of the patients were additionally assayed for ras mutations and compared with blood specimens. Our results indicate mutant K-ras DNA is readily detectable by PCR in the plasma or serum of patients with advanced colorectal cancer. Thus, plasma- or serum-based nucleic acid amplification assays may provide a valuable method of monitoring and potentially detecting colorectal cancer. IMAGES: |
format | Text |
id | pubmed-2228153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22281532009-09-10 Detection of mutant K-ras DNA in plasma or serum of patients with colorectal cancer. Kopreski, M. S. Benko, F. A. Kwee, C. Leitzel, K. E. Eskander, E. Lipton, A. Gocke, C. D. Br J Cancer Research Article Increased understanding of the molecular basis of colorectal cancer and recognition that extracellular DNA circulates in the plasma and serum of cancer patients enables new approaches to detection and monitoring. We used a polymerase chain reaction (PCR) assay to demonstrate mutant K-ras DNA in the plasma or serum of patients with colorectal cancer. Plasma or serum was fractionated from the blood of 31 patients with metastatic or unresected colorectal cancer and from 28 normal volunteers. DNA was extracted using either a sodium chloride or a gelatin precipitation method and then amplified in a two-stage PCR assay using selective restriction enzyme digestion to enrich for mutant K-ras DNA. Mutant K-ras DNA was detected in the plasma or serum of 12 (39%) patients, all confirmed by sequencing, but was not detected in any of the normal volunteers. K-ras mutations were detected in plasma or serum regardless of sex, primary tumour location, principal site of metastasis or proximity of chemotherapy and surgery to blood sampling. Tumour specimens available for 19 of the patients were additionally assayed for ras mutations and compared with blood specimens. Our results indicate mutant K-ras DNA is readily detectable by PCR in the plasma or serum of patients with advanced colorectal cancer. Thus, plasma- or serum-based nucleic acid amplification assays may provide a valuable method of monitoring and potentially detecting colorectal cancer. IMAGES: Nature Publishing Group 1997 /pmc/articles/PMC2228153/ /pubmed/9374374 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Kopreski, M. S. Benko, F. A. Kwee, C. Leitzel, K. E. Eskander, E. Lipton, A. Gocke, C. D. Detection of mutant K-ras DNA in plasma or serum of patients with colorectal cancer. |
title | Detection of mutant K-ras DNA in plasma or serum of patients with colorectal cancer. |
title_full | Detection of mutant K-ras DNA in plasma or serum of patients with colorectal cancer. |
title_fullStr | Detection of mutant K-ras DNA in plasma or serum of patients with colorectal cancer. |
title_full_unstemmed | Detection of mutant K-ras DNA in plasma or serum of patients with colorectal cancer. |
title_short | Detection of mutant K-ras DNA in plasma or serum of patients with colorectal cancer. |
title_sort | detection of mutant k-ras dna in plasma or serum of patients with colorectal cancer. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2228153/ https://www.ncbi.nlm.nih.gov/pubmed/9374374 |
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