Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: EC:2.7.7.48 (transcriptase)
 9,479 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Recent studies have shown a higher incidence of C-cell hyperplasia (CCH) in men compared with women in postmortem thyroid tissues. We postulated that the expression of androgen receptor (AR) protein may, in part, explain the differences. To test this hypothesis, we examined thyroid tissue from 27 consecutive autopsy cases for the presence of CCH (defined as >50 C-cells/x100 magnification in three fields) and for AR expression in autopsy cases and in 43 medullary thyroid carcinomas (MTCs) from patients with sporadic and familial disease as well as two multiple endocrine neoplasia type 2A patients with only CCH. CCH was present in 8 of 20 males (40%) and in 1 of 7 females (14%) at autopsy. AR protein was detected in most surgically resected thyroids with MTC and CCH (80%), but in only 25% of autopsy thyroids, probably reflecting postmortem degradation of the receptor protein. Reverse transcriptase polymerase chain reaction confirmed the presence of AR mRNA in MTC and in papillary thyroid carcinomas. These results support the observation that CCH is more common in postmortem thyroids of males and suggest that the presence of AR with higher circulating levels of androgens may contribute to the higher incidence of CCH in men.
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PMID:Androgen receptor expression in C-cells and in medullary thyroid carcinoma. 1285 7

The aim of the present study was to estimate the expression of mRNA, specific for thymidine kinase 1 (TK1), deoxycytidine kinase (dCK), and thymidine phosphorylase (dThdPase), i.e. enzymes involved in pyrimidine and purine metabolism in human papillary thyroid carcinoma (PTC) tissue. Additionally, the expression of dCK was estimated, in medullary thyroid carcinoma (MTC). For control, the RNA expression levels for all the enzymes were measured in macroscopically unchanged thyroid tissue. Reverse transcriptase-polymerase chain reaction (RT-PCR) and densitometry were employed for mRNA expression measurements, with the beta-actin gene as a control housekeeping gene. The levels of mRNA expression for TK1, dCK and dThdPase in human PTC, as well as mRNA expression for dCK in MTC, were significantly higher than mRNA expressions for those enzymes found in macroscopically unchanged thyroid tissue. It is concluded that an increased expression of mRNA, specific for TK1, dCK and dThdPase, may be involved in carcinogenic processes in the human thyroid.
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PMID:Increased expression of mRNA specific for thymidine kinase, deoxycytidine kinase or thymidine phosphorylase in human papillary thyroid carcinoma. 1597 30