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- Publisher Website: 10.1016/j.fertnstert.2007.10.020
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- PMID: 18191855
- WOS: WOS:000261566800017
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Article: Gene expression profiling of human peri-implantation endometria between natural and stimulated cycles
Title | Gene expression profiling of human peri-implantation endometria between natural and stimulated cycles | ||||||
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Authors | |||||||
Keywords | Endometrium implantation microarray steroid hormones stimulated cycle | ||||||
Issue Date | 2008 | ||||||
Publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/fertnstert | ||||||
Citation | Fertility And Sterility, 2008, v. 90 n. 6, p. 2152-2164 How to Cite? | ||||||
Abstract | Objective: To investigate the effect of high serum E 2 levels in gonadotropin-stimulated cycles (hCG+7) on the gene expression patterns of human endometrium compared with natural cycles on the seventh day of LH surge (LH+7) and elucidate the underlying molecular changes that may be related to endometrial receptivity. Design: Observational study. Setting: University Hospital. Patients(s): Infertile patients with normal menstrual cycles undergoing IVF treatment. Intervention(s): Gonadotropin stimulation and endometrial biopsy. Main Outcome Measure(s): Gene expression by microarray and quantitative polymerase chain reaction (qPCR). Result(s): Endometrial samples from natural (n = 5) and stimulated (n = 8) cycles were collected. Patients in the stimulated cycles were classified as moderate (n = 4) or excessive (n = 4) responders if their serum E 2 levels on the day of administration of hCG were ≤20,000 pmol/L or >20,000 pmol/L, respectively. The RNA transcripts were profiled by Affymetrix HG-U133A microarray. Clustering and principal component analysis demonstrated a significant difference (≥2-fold) in the expression patterns of 411 genes among the three groups. Putative estrogen response elements or progesterone response elements were identified in the promoter regions of 49 differentially expressed genes of diverse biologic functions. The qPCR confirmed the microarray result in 47 endometrial samples. Conclusion(s): High serum E 2 and/or progesterone modulate the gene expression profiles of human endometrium and may affect endometrial receptivity. © 2008 American Society for Reproductive Medicine. | ||||||
Persistent Identifier | http://hdl.handle.net/10722/60349 | ||||||
ISSN | 2023 Impact Factor: 6.6 2023 SCImago Journal Rankings: 1.858 | ||||||
ISI Accession Number ID |
Funding Information: Supported in part by grants from the Committee on Research and Conference Grant, University of Hong Kong, and the Hong Kong Research Grant Council (HKU 7514/05M). | ||||||
References | |||||||
Grants |
DC Field | Value | Language |
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dc.contributor.author | Liu, Y | en_HK |
dc.contributor.author | Lee, KF | en_HK |
dc.contributor.author | Ng, EHY | en_HK |
dc.contributor.author | Yeung, WSB | en_HK |
dc.contributor.author | Ho, PC | en_HK |
dc.date.accessioned | 2010-05-31T04:08:52Z | - |
dc.date.available | 2010-05-31T04:08:52Z | - |
dc.date.issued | 2008 | en_HK |
dc.identifier.citation | Fertility And Sterility, 2008, v. 90 n. 6, p. 2152-2164 | en_HK |
dc.identifier.issn | 0015-0282 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/60349 | - |
dc.description.abstract | Objective: To investigate the effect of high serum E 2 levels in gonadotropin-stimulated cycles (hCG+7) on the gene expression patterns of human endometrium compared with natural cycles on the seventh day of LH surge (LH+7) and elucidate the underlying molecular changes that may be related to endometrial receptivity. Design: Observational study. Setting: University Hospital. Patients(s): Infertile patients with normal menstrual cycles undergoing IVF treatment. Intervention(s): Gonadotropin stimulation and endometrial biopsy. Main Outcome Measure(s): Gene expression by microarray and quantitative polymerase chain reaction (qPCR). Result(s): Endometrial samples from natural (n = 5) and stimulated (n = 8) cycles were collected. Patients in the stimulated cycles were classified as moderate (n = 4) or excessive (n = 4) responders if their serum E 2 levels on the day of administration of hCG were ≤20,000 pmol/L or >20,000 pmol/L, respectively. The RNA transcripts were profiled by Affymetrix HG-U133A microarray. Clustering and principal component analysis demonstrated a significant difference (≥2-fold) in the expression patterns of 411 genes among the three groups. Putative estrogen response elements or progesterone response elements were identified in the promoter regions of 49 differentially expressed genes of diverse biologic functions. The qPCR confirmed the microarray result in 47 endometrial samples. Conclusion(s): High serum E 2 and/or progesterone modulate the gene expression profiles of human endometrium and may affect endometrial receptivity. © 2008 American Society for Reproductive Medicine. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/fertnstert | en_HK |
dc.relation.ispartof | Fertility and Sterility | en_HK |
dc.rights | Fertility and Sterility. Copyright © Elsevier Inc. | en_HK |
dc.subject | Endometrium | en_HK |
dc.subject | implantation | en_HK |
dc.subject | microarray | en_HK |
dc.subject | steroid hormones | en_HK |
dc.subject | stimulated cycle | en_HK |
dc.title | Gene expression profiling of human peri-implantation endometria between natural and stimulated cycles | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0015-0282&volume=90&spage=2152&epage=64&date=2008&atitle=Gene+expression+profiling+of+human+peri-implantation+endometria+between+natural+and+stimulated+cycles. | en_HK |
dc.identifier.email | Lee, KF:ckflee@hku.hk | en_HK |
dc.identifier.email | Ng, EHY:nghye@hkucc.hku.hk | en_HK |
dc.identifier.email | Yeung, WSB:wsbyeung@hkucc.hku.hk | en_HK |
dc.identifier.email | Ho, PC:pcho@hku.hk | en_HK |
dc.identifier.authority | Lee, KF=rp00458 | en_HK |
dc.identifier.authority | Ng, EHY=rp00426 | en_HK |
dc.identifier.authority | Yeung, WSB=rp00331 | en_HK |
dc.identifier.authority | Ho, PC=rp00325 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.fertnstert.2007.10.020 | en_HK |
dc.identifier.pmid | 18191855 | - |
dc.identifier.scopus | eid_2-s2.0-56949085051 | en_HK |
dc.identifier.hkuros | 158116 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-56949085051&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 90 | en_HK |
dc.identifier.issue | 6 | en_HK |
dc.identifier.spage | 2152 | en_HK |
dc.identifier.epage | 2164 | en_HK |
dc.identifier.eissn | 1556-5653 | - |
dc.identifier.isi | WOS:000261566800017 | - |
dc.publisher.place | United States | en_HK |
dc.relation.project | Role of olfactomedin in implantation | - |
dc.identifier.scopusauthorid | Liu, Y=23134878300 | en_HK |
dc.identifier.scopusauthorid | Lee, KF=26643097500 | en_HK |
dc.identifier.scopusauthorid | Ng, EHY=35238184300 | en_HK |
dc.identifier.scopusauthorid | Yeung, WSB=7102370745 | en_HK |
dc.identifier.scopusauthorid | Ho, PC=7402211440 | en_HK |
dc.identifier.issnl | 0015-0282 | - |