Abstract | OBJECTIVE: METHOD: Benign and malignant tissues, preserved in paraffin blocks and separated by microdissection, were examined using a commercial PCR-based tissue identity assay (ABI AmpFlSTR Profiler Plus Kit and ABI 377 DNA sequencer) to detect genetic profiles of 9 microsatellite markers, along with X and Y chromosome markers. Cases included 6 choriocarcinomas. Controls included eight non-germ cell reproductive tract tumors and two hydatidiform moles. RESULTS: The microsatellite markers identified the five choriocarcinomas diagnosed on clinical and histological grounds as gestational, to be of genetically non-maternal (androgenic) origin. The neoplasm previously classified as a non-gestational choriocarcinoma was demonstrated to be of maternal origin, as were the non-germ cell reproductive tract tumors. Samples from hydatidiform moles contained either androgenic markers only or a mix of maternal and androgenic markers, as previously seen in complete and partial moles, respectively. CONCLUSION:
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Authors | Milena Cankovic, Arthur R Gaba, Frederick Meier, Wooshin Kim, Richard J Zarbo |
Journal | Gynecologic oncology
(Gynecol Oncol)
Vol. 103
Issue 2
Pg. 614-7
(Nov 2006)
ISSN: 0090-8258 [Print] United States |
PMID | 16740299
(Publication Type: Journal Article)
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Chemical References |
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Topics |
- Alleles
- Case-Control Studies
- Choriocarcinoma
(genetics)
- Choriocarcinoma, Non-gestational
(genetics)
- DNA, Neoplasm
(genetics)
- Fallopian Tube Neoplasms
(genetics)
- Female
- Humans
- Lung Neoplasms
(genetics)
- Microsatellite Repeats
(genetics)
- Ovarian Neoplasms
(genetics)
- Polymerase Chain Reaction
(methods)
- Pregnancy
- Uterine Neoplasms
(genetics)
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