Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0476089 (endometrial cancer)
 11,379 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Sialyl SSEA-1 antigen (SLX) is a highly specific tumor marker composed of sugar chain antigens that have Lewis X at their terminals and bind to sialic acid. This antigen is rarely detected in normal tissues, and is present in adenocarcinoma and fetal tissues. We studied the clinical usefulness of SLX in gynecological patients and obtained the following results. (1) The antigen was frequently positive in patients with ovarian cancer with a mean of 89.5 +/- 48.3 U/ml (72.8%, 8/11) and in those with endometriosis with a mean of 39.8 +/- 10.3 U/ml (75.0%, 6/8). (2) Among the gynecological malignancies, the percent positivity was low in those with cervical cancer (20.0%, 5/25), endometrial cancer (33.3%, 1/3), and cancer of the fallopian tube (33.3%, 1/3). (3) The antigen was negative in 20 with myoma uteri, 20 normal pregnant women, and 9 nonpregnant healthy women during the follicular, luteal, or menstrual phase. It was negative in 8 of 9 patients with benign ovarian cyst. False negative results were rare. (4) The SLX level was higher in the ascites than in the serum in patients with ovarian cancer and in those with benign ovarian tumors. (5) The serum SLX in patients with ovarian cancer, which was positive before tumor resection, became negative 2 weeks postoperatively. These results suggest that SLX is a tumor marker with a high specificity to adenocarcinoma of the reproductive organs.
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PMID:Clinical evaluations of the tumor marker sialyl SSEA-1 antigen for clinical gynecological disease. 197 88

Galactosyltransferase Associated with Tumor (GAT) was clinically studied in cases of ovarian cancer. When two cut-off levels of GAT were compared, the cut-off level of 16 U/ml (which corresponds to mean + 2SD among healthy females) was found to be more suitable than the cut-off level of 14 U/ml (the level maximizing the diagnostic efficiency between malignant and benign ovarian tumors). When the GAT positive rate was examined for gynecologic tumors, the rate was 5.7% for benign ovarian cyst, 6.6% for endometriosis, 20.5% for cervical cancer, 19.5% for endometrial cancer, and 52.9% for ovarian cancer. The GAT positive rate for different histologic types of ovarian carcinoma was relatively high for each type, e.g., 55.0% for clear cell adenocarcinoma and 66.7% for endometrioid adenocarcinoma. The GAT positive rate increased gradually with the stage of ovarian cancer. In patients with benign diseases, in particular endometriosis, the GAT positive rate was lower than the positive rate with any other simultaneously determined marker (CA602, CA125, CA54/61, CA72-4, STN, and SLX). The GAT level most weakly correlated with the level of any of the other markers assessed. An assay combining GAT with CA602 or CA54/61 resulted in a higher positive rate and a higher diagnostic efficiency, when compared with the assay for GAT alone. The lower positive rate of GAT in endometriosis, when compared with the positive rate of other markers, suggests the usefulness of GAT in distinguishing malignant ovarian tumors from benign ovarian tumors. The use of GAT in a combination assay is expected to overcome the disadvantages of CA602 or CA125.
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PMID:[Preclinical and clinical studies on a tumor marker, galactosyltransferase associated with tumor (GAT), in ovarian cancer (second report)--clinical significance of GAT and comparison with other tumor markers]. 843 67

A 47 year old patient with a G3, FIGO stage 1A endometrial cancer was treated by hysterectomy. Her two ovaries were conserved because of the pre-operative diagnosis of endocervical cancer. On follow up PET-CT follow up investigation, she had a benign ovarian corpus luteal cyst mistaken as a metastatic pelvic lymph node which was later removed and proven benign histologically. This paper is to raise the clinical awareness of possible false positive PET finding from a benign ovarian cyst, such that a misinterpretation of "recurrence" as in this case can be avoided.
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PMID:A false positive fluorodeoxyglucose positron emission tomography/computed tomography diagnosis of pelvic lymph node recurrence following surgical treatment of Stage 1 endometrial cancer-a case report. 3025 95