Analysis of oncogene alterations in human endometrial carcinoma: Prevalence of ras mutations

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Abstract
The molecular genetics of human endometrial carcinoma have yet to be defined to any significant extent. Cell lines from 11 endometrial carcinomas were examined for alterations in proto‐oncogenes that might predictably be present, based on existing data from the better‐characterized human carcinomas of the uterine cervix, ovary, and breast. Codons 12, 13, and 61 of the Ha‐ras, Ki‐ras, and N‐ras genes were examined for possible point mutations, and the c‐erbB2/neu, c‐myc, and epidermal growth factor receptor (EGFR) genes were examined for amplification or overexpression. Ras mutations were found in seven of 11 (64%) tumors, including three in codon 61 of Ha‐ras (CAG·CAT) and four in codon 12 of Ki‐ras (GGT→GAT in two and GGT→GTT in two). No evidence was found for amplification or overexpression of the c‐enbB2 or EGFR genes in any tumor. One tumor contained amplified c‐myc sequences and exhibited relative overexpression of c‐myc. These data suggest that the amplification or overexpression of several proto‐oncogenes frequently observed in other human gynecologic and breast tumors are not prevalent in endometrial carcinoma and that ras gene mutations are relatively common in this tumor type.