Abstract

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.

Highlights

  • We confirm that mutant K-ras DNA is readily detectable in the blood of patients with colorectal cancer, but not in the blood of normal volunteers. These findings suggest that analysis of blood plasma or serum for mutant oncogene DNA might provide a valuable method of monitoring and potentially diagnosing patients with colorectal cancer

  • polymerase chain reaction (PCR) was performed on blood plasma and serum, primary tumours and lymph node metastases

  • Plasma and serum specimens All 28 plasma and serum specimens from normal volunteers tested negative for mutant K-ras DNA regardless of extraction method used

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Summary

Methods

Five to ten millilitres of peripheral blood were collected from 31 patients with metastatic (30 patients) or unresected primary (one patient) colorectal cancer and from 28 normal volunteers. Blood was centrifuged at 4°C and 850 g for 10 min, the plasma (22 patients, 28 normal volunteers) or serum (nine patients) fraction was removed and stored frozen at - 70°C. 15 were collected prospectively and were stored for 1-6 months before assaying. The remaining 16 samples had been collected in 1988 and had been stored for more than 6 years before assaying. All normal volunteer samples had been collected recently and had been frozen for a short time. Paraffin blocks of tumours were available for 19 patients, including 18 primary tumours and four metastatic lymph node specimens

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