Mutations in the p53 gene are associated with a wide variety of human malignancies. Point mutation in one allele and loss of the remaining one generally lead to inactivation of p53 protein. A high frequency of allelic losses corresponding to the I7p 13.3 region that contained the p53 gene sequence
DCC gene alteration in human endometrial carcinomas
β Scribed by Tomonao Gima; Hidenori Kato; Tsuyoshi Honda; Toshiro Imamura; Takehiko Sasazuki; Norio Wake
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- French
- Weight
- 951 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0020-7136
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β¦ Synopsis
Abstract
The present study was undertaken to define the gene(s) of importance on the long arm of chromosome 18 (chromosome 18q) in endometrial carcinomas. We analyzed loss of heterozygosity (LOH) at 3 loci on chromosome 18q and DCC gene expression by the reverseβtranscriptase/polymerase chain reaction (RTβPCR) method. Among 61 tumors that were informative, 16 (26%), estimated to be a minimum number, showed allelic losses at one or more chromosome 18q loci. Deletions in these tumors possibly involved the region within or near the chromosome 18q 21.3 band where the DCC gene was localized. Moreover, the incidence of altered DCC mRNA expression was high in these tumors. Appropriate transcription was lost in 5 of 7 (71%) carcinoma cell lines in addition to 14 of 28 (50%) surgically resected tumors. Histopathological differentiation and clinical stage of disease were not related to LOH frequency or to DCC mRNA expression. These results suggest that the target for allelic loss on chromosome 18q seen in endometrial carcinomas is the DCC gene, and that inactivation of this gene may be critical for the development of most endometrial carcinomas. Β© 1994 WileyβLiss, Inc.
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