Testosterone metabolism in the human endometrium : a combination of metabolic (mass spectrometry) and enzyme expression (RT-PCR)
Localised steroid metabolism is important in proliferative disorders of the endometrium. The metabolism of testosterone, an important precursor in endometrial disorders, was investigated by mass spectrometry and RT-PCR (real-time polymerase chain reaction), allowing determination of steroid metaboli...
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ndltd-bl.uk-oai-ethos.bl.uk-7522062018-10-09T03:21:51ZTestosterone metabolism in the human endometrium : a combination of metabolic (mass spectrometry) and enzyme expression (RT-PCR)Taylor, Angela Elizabeth2009Localised steroid metabolism is important in proliferative disorders of the endometrium. The metabolism of testosterone, an important precursor in endometrial disorders, was investigated by mass spectrometry and RT-PCR (real-time polymerase chain reaction), allowing determination of steroid metabolites and expression of steroid converting enzymes; aromatase, 17P-HSD1, 2,4,5,7,8,(hydroxysteroid dehydrogenase) and 5AR1, 2 (alpha reductase). Samples were derived from cell lines (Ishikawa, HEC-1A, HEC-1B, RL95-2, COV434), and biopsies; fertile, endometriosis, poly-cystic ovary syndrome (PCOS), endometrial hyperplasia, unexplained infertility, endometrial polyp. Optimum mass spectrometry techniques, determined using steroid standards, were LC/MS for androgens and LC/MS/MS for oestrogens, following dansyl-chloride derivatisation. GC/MS was less sensitive. The route of testosterone metabolism varied in the cell lines and clinical biopsies, the major metabolite was correlated with high expression of 5AR1 or 17p-HSD2, 4 and 8. If DHT (dihydrotestosterone) was produced high basal expression of 5AR1 was observed and if androstenedione was produced high basal expression of HSD2, 4 or 8 was observed. A mixture of DHT and androstenedione was correlated with expression of 5AR1 and 17P-HSD2, 4 or HSD 8. Changes in enzyme expression were correlated with changes in steroid concentration after testosterone treatment, as follows: 1. Increased 5AR1 expression was correlated with increased DHT concentration in Ishikawa, HEC-1B, COV434, PCOS, endometriosis, stromal hyperplasia and ovarian cyst biopsies. 2. Increased expression of 5AR2 was correlated with increased androsterone concentration in fertile and unexplained infertility biopsies. 3. Increased 17p-HSD5 expression was correlated with increased testosterone concentration in HEC-1A cells. 4. Increased aromatase expression was correlated to increased oestradiol and oestrone concentrations in a hyperplasia biopsy. Analysis of a range of enzymes and steroids produced testosterone metabolism maps of the endometrium (and associated disorders) highlighting steroids which could contribute to endometrial disorders and viable enzyme target(s) for inhibition (5AR1,17P-HSD2, 4, 8).Swansea University https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.752206https://cronfa.swan.ac.uk/Record/cronfa43059Electronic Thesis or Dissertation |
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Localised steroid metabolism is important in proliferative disorders of the endometrium. The metabolism of testosterone, an important precursor in endometrial disorders, was investigated by mass spectrometry and RT-PCR (real-time polymerase chain reaction), allowing determination of steroid metabolites and expression of steroid converting enzymes; aromatase, 17P-HSD1, 2,4,5,7,8,(hydroxysteroid dehydrogenase) and 5AR1, 2 (alpha reductase). Samples were derived from cell lines (Ishikawa, HEC-1A, HEC-1B, RL95-2, COV434), and biopsies; fertile, endometriosis, poly-cystic ovary syndrome (PCOS), endometrial hyperplasia, unexplained infertility, endometrial polyp. Optimum mass spectrometry techniques, determined using steroid standards, were LC/MS for androgens and LC/MS/MS for oestrogens, following dansyl-chloride derivatisation. GC/MS was less sensitive. The route of testosterone metabolism varied in the cell lines and clinical biopsies, the major metabolite was correlated with high expression of 5AR1 or 17p-HSD2, 4 and 8. If DHT (dihydrotestosterone) was produced high basal expression of 5AR1 was observed and if androstenedione was produced high basal expression of HSD2, 4 or 8 was observed. A mixture of DHT and androstenedione was correlated with expression of 5AR1 and 17P-HSD2, 4 or HSD 8. Changes in enzyme expression were correlated with changes in steroid concentration after testosterone treatment, as follows: 1. Increased 5AR1 expression was correlated with increased DHT concentration in Ishikawa, HEC-1B, COV434, PCOS, endometriosis, stromal hyperplasia and ovarian cyst biopsies. 2. Increased expression of 5AR2 was correlated with increased androsterone concentration in fertile and unexplained infertility biopsies. 3. Increased 17p-HSD5 expression was correlated with increased testosterone concentration in HEC-1A cells. 4. Increased aromatase expression was correlated to increased oestradiol and oestrone concentrations in a hyperplasia biopsy. Analysis of a range of enzymes and steroids produced testosterone metabolism maps of the endometrium (and associated disorders) highlighting steroids which could contribute to endometrial disorders and viable enzyme target(s) for inhibition (5AR1,17P-HSD2, 4, 8). |
author |
Taylor, Angela Elizabeth |
spellingShingle |
Taylor, Angela Elizabeth Testosterone metabolism in the human endometrium : a combination of metabolic (mass spectrometry) and enzyme expression (RT-PCR) |
author_facet |
Taylor, Angela Elizabeth |
author_sort |
Taylor, Angela Elizabeth |
title |
Testosterone metabolism in the human endometrium : a combination of metabolic (mass spectrometry) and enzyme expression (RT-PCR) |
title_short |
Testosterone metabolism in the human endometrium : a combination of metabolic (mass spectrometry) and enzyme expression (RT-PCR) |
title_full |
Testosterone metabolism in the human endometrium : a combination of metabolic (mass spectrometry) and enzyme expression (RT-PCR) |
title_fullStr |
Testosterone metabolism in the human endometrium : a combination of metabolic (mass spectrometry) and enzyme expression (RT-PCR) |
title_full_unstemmed |
Testosterone metabolism in the human endometrium : a combination of metabolic (mass spectrometry) and enzyme expression (RT-PCR) |
title_sort |
testosterone metabolism in the human endometrium : a combination of metabolic (mass spectrometry) and enzyme expression (rt-pcr) |
publisher |
Swansea University |
publishDate |
2009 |
url |
https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.752206 |
work_keys_str_mv |
AT taylorangelaelizabeth testosteronemetabolisminthehumanendometriumacombinationofmetabolicmassspectrometryandenzymeexpressionrtpcr |
_version_ |
1718772133319933952 |