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Article: Human chorionic gonadotropin stimulates spheroid attachment on fallopian tube epithelial cells through the mitogen-activated protein kinase pathway and down-regulation of olfactomedin-1
Title | Human chorionic gonadotropin stimulates spheroid attachment on fallopian tube epithelial cells through the mitogen-activated protein kinase pathway and down-regulation of olfactomedin-1 |
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Authors | |
Keywords | fallopian tube MAPK signaling Olfactomedin-1 tubal ectopic pregnancy Wnt-signaling |
Issue Date | 2015 |
Publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/fertnstert |
Citation | Fertility and Sterility, 2015, v. 104 n. 2, p. 474-482 How to Cite? |
Abstract | OBJECTIVE: To study the effect of human chorionic gonadotropin (hCG) on olfactomedin-1 (Olfm1) expression and spheroid attachment in human fallopian tube epithelial cells in vitro. DESIGN: Experimental study. SETTING: Reproductive biology laboratory. PATIENT(S): Healthy non-pregnant women. INTERVENTION(S): No patient interventions. MAIN OUTCOME MEASURE(S): Luteinizing hormone/chorionic gonadotropin receptor (LHCGR) and Olfm1 expression in fallopian tube epithelium cell line (OE-E6/E7 cells). OE-E6/E7 cells treated with hCG, U0126 extracellular signal-regulated kinase (ERK) inhibitor, or XAV939 Wnt/β-catenin inhibitor were analyzed by Western blotting, real-time polymerase chain reaction, and in vitro spheroid attachment assay. RESULT(S): Human chorionic gonadotropin increased spheroid attachment on OE-E6/E7 cells through down-regulation of Olfm1 and activation of Wnt and mitogen-activated protein kinase (MAPK) signaling pathways. U0126 down-regulated both MAPK and Wnt/β-catenin signaling pathways and up-regulated Olfm1 expression. XAV939 down-regulated only the Wnt/β-catenin signaling pathway but up-regulated Olfm1 expression. CONCLUSION(S): Human chorionic gonadotropin activated both ERK and Wnt/β-catenin signaling pathways and enhanced spheroid attachment on fallopian tube epithelial cells through down-regulation of Olfm1 expression. |
Persistent Identifier | http://hdl.handle.net/10722/214727 |
ISSN | 2023 Impact Factor: 6.6 2023 SCImago Journal Rankings: 1.858 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | So, KH | - |
dc.contributor.author | Kodithuwakku, SPK | - |
dc.contributor.author | Kottawatta, KSA | - |
dc.contributor.author | Li, RHW | - |
dc.contributor.author | Chiu, PCN | - |
dc.contributor.author | Cheung, ANY | - |
dc.contributor.author | Ng, EHY | - |
dc.contributor.author | Yeung, WSB | - |
dc.contributor.author | Lee, CKF | - |
dc.date.accessioned | 2015-08-21T11:53:01Z | - |
dc.date.available | 2015-08-21T11:53:01Z | - |
dc.date.issued | 2015 | - |
dc.identifier.citation | Fertility and Sterility, 2015, v. 104 n. 2, p. 474-482 | - |
dc.identifier.issn | 0015-0282 | - |
dc.identifier.uri | http://hdl.handle.net/10722/214727 | - |
dc.description.abstract | OBJECTIVE: To study the effect of human chorionic gonadotropin (hCG) on olfactomedin-1 (Olfm1) expression and spheroid attachment in human fallopian tube epithelial cells in vitro. DESIGN: Experimental study. SETTING: Reproductive biology laboratory. PATIENT(S): Healthy non-pregnant women. INTERVENTION(S): No patient interventions. MAIN OUTCOME MEASURE(S): Luteinizing hormone/chorionic gonadotropin receptor (LHCGR) and Olfm1 expression in fallopian tube epithelium cell line (OE-E6/E7 cells). OE-E6/E7 cells treated with hCG, U0126 extracellular signal-regulated kinase (ERK) inhibitor, or XAV939 Wnt/β-catenin inhibitor were analyzed by Western blotting, real-time polymerase chain reaction, and in vitro spheroid attachment assay. RESULT(S): Human chorionic gonadotropin increased spheroid attachment on OE-E6/E7 cells through down-regulation of Olfm1 and activation of Wnt and mitogen-activated protein kinase (MAPK) signaling pathways. U0126 down-regulated both MAPK and Wnt/β-catenin signaling pathways and up-regulated Olfm1 expression. XAV939 down-regulated only the Wnt/β-catenin signaling pathway but up-regulated Olfm1 expression. CONCLUSION(S): Human chorionic gonadotropin activated both ERK and Wnt/β-catenin signaling pathways and enhanced spheroid attachment on fallopian tube epithelial cells through down-regulation of Olfm1 expression. | - |
dc.language | eng | - |
dc.publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/fertnstert | - |
dc.relation.ispartof | Fertility and Sterility | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | fallopian tube | - |
dc.subject | MAPK signaling | - |
dc.subject | Olfactomedin-1 | - |
dc.subject | tubal ectopic pregnancy | - |
dc.subject | Wnt-signaling | - |
dc.title | Human chorionic gonadotropin stimulates spheroid attachment on fallopian tube epithelial cells through the mitogen-activated protein kinase pathway and down-regulation of olfactomedin-1 | - |
dc.type | Article | - |
dc.identifier.email | Li, RHW: raymondli@hku.hk | - |
dc.identifier.email | Chiu, PCN: pchiucn@hku.hk | - |
dc.identifier.email | Cheung, ANY: anycheun@hkucc.hku.hk | - |
dc.identifier.email | Ng, EHY: nghye@hku.hk | - |
dc.identifier.email | Yeung, WSB: wsbyeung@hku.hk | - |
dc.identifier.email | Lee, CKF: ckflee@hku.hk | - |
dc.identifier.authority | Li, RHW=rp01649 | - |
dc.identifier.authority | Chiu, PCN=rp00424 | - |
dc.identifier.authority | Cheung, ANY=rp00542 | - |
dc.identifier.authority | Ng, EHY=rp00426 | - |
dc.identifier.authority | Yeung, WSB=rp00331 | - |
dc.identifier.authority | Lee, CKF=rp00458 | - |
dc.description.nature | postprint | - |
dc.identifier.doi | 10.1016/j.fertnstert.2015.04.030 | - |
dc.identifier.pmid | 25999259 | - |
dc.identifier.scopus | eid_2-s2.0-84938293127 | - |
dc.identifier.hkuros | 249070 | - |
dc.identifier.volume | 104 | - |
dc.identifier.issue | 2 | - |
dc.identifier.spage | 474 | - |
dc.identifier.epage | 482 | - |
dc.identifier.isi | WOS:000363954000032 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0015-0282 | - |