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Published on: July 25, 2020
Amplification of protooncogenes in human ovarian carcinomas
T Liehr1, N Atanasov, H Tulusan
1UNIV ERLANGEN NURNBERG,INST HUMAN GENET,SCHWABACHANLAGE 10,W-8520 ERLANGEN,GERMANY. UNIV ERLANGEN NURNBERG,GYNECOL CLIN,W-8520 ERLANGEN,GERMANY.
Abstract:
Amplification of the proto-oncogenes c-myc, c-erbB2, c-K-ras2, c-H-ras1, c-erbA1, c-int2 and c-fms was studied by Southern-blot analysis of DNA extracted from 27 primary ovarian carcinomas. In addition, karyotype analysis and interphase cytogenetics using fluorescence in situ hybridization (FISH) were applied to control the chromosomal variability of the tumors. By these additional analyses the possibility of a false estimation of the grades of amplification should be diminished. In nearly 50% of the studied tumors a low to moderate (2- to 10-fold) amplification of one or more oncogenes was detected. The proto-oncogene amplified most frequently was c-myc (11 tumors), followed by c-erbB2 and c-Kras2 (3 tumors each), c-fms (2 tumors), and c-int2 (1 tumor). Neither an amplification of c-erbA1 nor of c-H-ras1 could be detected in any of the tumors. Some of the tumors showed a simultaneous amplification of two or three oncogenes. The pattern of proto-oncogene amplification clearly differentiates the studied ovarian cancers from breast tumors, but also differs from some previous results obtained from ovarian carcinomas.
Insights
Nearly half of ovarian carcinomas showed amplified oncogenes, with c-myc being the most frequent. This proto-oncogene amplification pattern distinguishes ovarian from breast tumors.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Proto-oncogene amplification is implicated in various cancers.
- Understanding oncogene alterations in ovarian cancer is crucial for diagnosis and treatment.
- Previous studies show varied results in ovarian carcinoma oncogene amplification.
Purpose of the Study:
- To investigate the amplification of specific proto-oncogenes in primary ovarian carcinomas.
- To correlate oncogene amplification patterns with tumor characteristics.
- To differentiate ovarian cancer oncogene profiles from other cancers.
Main Methods:
- Southern-blot analysis of DNA from 27 primary ovarian carcinomas.
- Karyotype analysis and fluorescence in situ hybridization (FISH) for chromosomal control.
- Quantification of oncogene amplification levels (2- to 10-fold).
Main Results:
- Nearly 50% of tumors exhibited low to moderate amplification of one or more oncogenes.
- c-myc was the most frequently amplified proto-oncogene (11 tumors).
- c-erbB2 and c-Kras2 were amplified in 3 tumors each; c-fms in 2; c-int2 in 1.
- No amplification of c-erbA1 or c-H-ras1 was detected.
- Some tumors showed simultaneous amplification of multiple oncogenes.
Conclusions:
- Proto-oncogene amplification is a common event in ovarian carcinomas.
- The specific pattern of oncogene amplification in these ovarian cancers differs from breast tumors and some prior ovarian cancer findings.
- FISH and karyotype analysis help validate Southern-blot results, reducing false amplification estimations.
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