Differential mRNA expression profiling in ovarian endometriotic tissue with versus without leuprolide acetate treatment. Issue 10 (15th September 2015)
- Record Type:
- Journal Article
- Title:
- Differential mRNA expression profiling in ovarian endometriotic tissue with versus without leuprolide acetate treatment. Issue 10 (15th September 2015)
- Main Title:
- Differential mRNA expression profiling in ovarian endometriotic tissue with versus without leuprolide acetate treatment
- Authors:
- Kiba, Atsushi
Banno, Kouji
Yanokura, Megumi
Asada, Mari
Nakayama, Yusuke
Aoki, Daisuke
Watanabe, Tatsuya - Abstract:
- <abstract abstract-type="main"> <title> <bold>Abstract</bold> </title> <sec id="jog12768-sec-0001" sec-type="section"> <title>Aim</title> <p>Leuprolide acetate, an analog of gonadotropin‐releasing hormone (GnRH), regresses endometriotic tissue and reduces pain, resulting in clinical improvement upon treatment. The molecular mechanisms involved in the regression of endometriotic tissue, however, remain to be elucidated. In this study, we performed genome‐wide gene expression profiling of clinical specimens of ovarian endometrioma to obtain insight into the effects of leuprolide acetate treatment.</p> </sec> <sec id="jog12768-sec-0002" sec-type="section"> <title>Methods</title> <p>We obtained clinical samples from nine normal eutopic endometrium tissues, eight ovarian endometriotic tissues, and 12 leuprolide acetate‐treated endometriotic tissues. We compared the gene expression profiles of the three groups using Affymetrix GeneChip Human genome arrays and bioinformatic analysis, including molecular concept analysis.</p> </sec> <sec id="jog12768-sec-0003" sec-type="section"> <title>Results</title> <p>Leuprolide acetate‐treated endometriotic tissue showed downregulated genes associated with the biological functions of steroid hormone regulation, cell proliferation, inflammation, and intracellular signaling. These genes included <italic>PTGDS, GRP, APLP2, PLTP, </italic> and <italic>FGFRL1</italic>. In contrast, genes upregulated by leuprolide acetate treatment were associated<abstract abstract-type="main"> <title> <bold>Abstract</bold> </title> <sec id="jog12768-sec-0001" sec-type="section"> <title>Aim</title> <p>Leuprolide acetate, an analog of gonadotropin‐releasing hormone (GnRH), regresses endometriotic tissue and reduces pain, resulting in clinical improvement upon treatment. The molecular mechanisms involved in the regression of endometriotic tissue, however, remain to be elucidated. In this study, we performed genome‐wide gene expression profiling of clinical specimens of ovarian endometrioma to obtain insight into the effects of leuprolide acetate treatment.</p> </sec> <sec id="jog12768-sec-0002" sec-type="section"> <title>Methods</title> <p>We obtained clinical samples from nine normal eutopic endometrium tissues, eight ovarian endometriotic tissues, and 12 leuprolide acetate‐treated endometriotic tissues. We compared the gene expression profiles of the three groups using Affymetrix GeneChip Human genome arrays and bioinformatic analysis, including molecular concept analysis.</p> </sec> <sec id="jog12768-sec-0003" sec-type="section"> <title>Results</title> <p>Leuprolide acetate‐treated endometriotic tissue showed downregulated genes associated with the biological functions of steroid hormone regulation, cell proliferation, inflammation, and intracellular signaling. These genes included <italic>PTGDS, GRP, APLP2, PLTP, </italic> and <italic>FGFRL1</italic>. In contrast, genes upregulated by leuprolide acetate treatment were associated with cell growth inhibition and apoptosis. These genes included <italic>CARD11</italic> and <italic>USP18</italic>.</p> </sec> <sec id="jog12768-sec-0004" sec-type="section"> <title>Conclusions</title> <p>These preliminary results based on GeneChip analysis suggest that leuprolide acetate treatment induces a modulation of gene expression that allows for cooperative alterations in disease state. This study gives new insight into the effects of leuprolide acetate treatment. Further investigations with quantitative reverse transcription–polymerase chain reaction and immunohistochemistry are needed to validate this study and to explore new therapeutic targets and biomarkers of endometriosis.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of obstetrics and gynaecology research. Volume 41:Issue 10(2015:Oct.)
- Journal:
- Journal of obstetrics and gynaecology research
- Issue:
- Volume 41:Issue 10(2015:Oct.)
- Issue Display:
- Volume 41, Issue 10 (2015)
- Year:
- 2015
- Volume:
- 41
- Issue:
- 10
- Issue Sort Value:
- 2015-0041-0010-0000
- Page Start:
- 1598
- Page End:
- 1606
- Publication Date:
- 2015-09-15
- Subjects:
- Gynecology -- Periodicals
Obstetrics -- Periodicals
618.1005 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1447-0756 ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=jog ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/jog.12768 ↗
- Languages:
- English
- ISSNs:
- 1341-8076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5026.055000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4015.xml