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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Main Author: Taylor, Angela Elizabeth
Published: Swansea University 2009
Online Access:https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.752206
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spelling 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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description 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
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