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DCC gene alteration in human endometrial carcinomas
1Department of Reproductive Physiology and Endocrinology, Kyushu University, Oita, Japan.
International Journal of Cancer
|May 15, 1994
Summary
Loss of heterozygosity (LOH) on chromosome 18q and DCC gene expression were analyzed in endometrial carcinomas. Inactivation of the DCC gene may be critical for endometrial cancer development.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Endometrial carcinoma is a significant gynecological malignancy.
- Chromosome 18q alterations are implicated in various cancers.
- The DCC gene's role in endometrial cancer requires further elucidation.
Purpose of the Study:
- To identify critical genes on chromosome 18q in endometrial carcinomas.
- To investigate the association between loss of heterozygosity (LOH) and DCC gene expression.
- To determine the potential role of the DCC gene in endometrial carcinogenesis.
Main Methods:
- Analysis of LOH at three loci on chromosome 18q in 61 endometrial tumors.
- Assessment of DCC gene expression using reverse-transcriptase/polymerase chain reaction (RT-PCR).
- Correlation of genetic alterations with histopathological differentiation and clinical stage.
Main Results:
- A minimum of 26% of informative tumors exhibited LOH at chromosome 18q loci.
- High incidence of altered DCC mRNA expression observed in tumors and cell lines (50% and 71%, respectively).
- No significant correlation found between LOH/DCC expression and tumor differentiation or clinical stage.
Conclusions:
- The DCC gene is a likely target for allelic loss on chromosome 18q in endometrial carcinomas.
- Inactivation of the DCC gene may play a critical role in the development of endometrial cancer.
- Further research into DCC gene function is warranted for therapeutic strategies.