Molecular detection of tumour DNA in serum and peritoneal fluid from ovarian cancer patients
1999

Detecting Tumor DNA in Ovarian Cancer Patients

Sample size: 20 publication Evidence: moderate

Author Information

Author(s): Hickey K P, Boyle K P, Jepps H M, Andrew A C, Buxton E J, Burns P A

Primary Institution: Leeds General Infirmary, University of Leeds

Hypothesis

Can tumor-specific genetic alterations be detected in the serum and peritoneal fluid of ovarian cancer patients?

Conclusion

Molecular detection methods can effectively identify tumor-specific alterations in ovarian cancer patients' serum and peritoneal fluid.

Supporting Evidence

  • Tumour-specific abnormalities were detected in the serum of all but one of the stage Ia cases.
  • Half of the occurrences of loss of heterozygosity identified in primary tumour material were detectable in the serum samples.
  • Novel alleles indicative of microsatellite instability were found in 3/6 patients with stage Ia disease.

Takeaway

Doctors can find signs of cancer in the blood and fluid around the belly of women with ovarian cancer using special tests.

Methodology

DNA was extracted from serum and peritoneal fluid of ovarian cancer patients and analyzed for tumor-specific genetic alterations using six polymorphic microsatellite loci.

Limitations

The study had a small sample size and included only a limited number of genetic markers.

Participant Demographics

20 ovarian cancer patients, including six with stage Ia disease.

Digital Object Identifier (DOI)

10.1038/sj.bjc.6690601

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