Cited by 15Ectopic Pregnancy Diagnosis and ManagementReproductive System and PregnancyReproductive Health and Contraception

Gonadotropin-releasing hormone and gonadotropin-releasing hormone receptor are expressed at tubal ectopic pregnancy implantation sites

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Peng, Bo, Klausen, Christian, Campbell, Lisa, Leung, Peter C.K., Horne, Andrew W., Bedaiwy, Mohamed A.·2016·Fertility and Sterility

Abstract

Objective To investigate whether gonadotropin-releasing hormone (GnRH) and GnRH receptor (GnRHR) are expressed at tubal ectopic pregnancy sites, and to study the potential role of GnRH signaling in regulating immortalized human trophoblast cell viability.Design Immunohistochemical and experimental studies.Setting Academic research laboratory.Patient(s) Fallopian tube implantation sites (n = 25) were collected from women with ectopic pregnancy. First-trimester human placenta biopsies (n = 5) were obtained from elective terminations of pregnancy.Intervention(s) None.Main outcome measure(s) GnRH and GnRHR expression was examined by means of immunohistochemistry and histoscoring. Trophoblastic BeWo choriocarcinoma and immortalized extravillous trophoblast (HTR-8/SVneo) cell viability was examined by means of cell counting after incubation with GnRH and/or GnRH antagonist (Antide).Result(s) GnRH and GnRHR immunoreactivity was detected in cytotrophoblast, syncytiotrophoblast, and extravillous trophoblast in all women with tubal pregnancy. GnRH immunoreactivity was higher and GnRHR immunoreactivity lower in syncytiotrophoblast compared with cytotrophoblast. GnRH and GnRHR immunoreactivity was detected in adjacent fallopian tube epithelium. Whereas neither GnRH nor Antide altered HTR-8/SVneo cell viability, treatment with GnRH significantly increased the overall cell viability of BeWo cells at 48 and 72 hours, and these effects were abolished by pretreatment with Antide.Conclusion(s) GnRH and GnRHR are expressed in trophoblast cell populations and fallopian tube epithelium at tubal ectopic pregnancy sites. GnRH increases BeWo cell viability, an effect mediated by the GnRHR. Further work is required to investigate the potential role of GnRH signaling in ectopic pregnancy.

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Crossref · 10.1016/j.fertnstert.2016.02.003

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  1. Klein M, Graf AH, Hutter W, Hacker GW, Beck A, Staudach A, et al. Prolifer- ative activity in ectopic trophoblastic tissue. Hum Reprod 1995;10:2441-4.

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Authors
Peng, B., Klausen, C., Campbell, L., Leung, P. C. K., Horne, A. W., & Bedaiwy, M. A.
Affiliations
  • University of British Columbia (CA)
  • MRC Centre for Reproductive Health (GB)
Corresponding author
Bedaiwy, Mohamed A.
Venue
Fertility and Sterility
Publisher
Elsevier BV
Published
2016-06
Volume
105
Issue
6
Pages
1620-1627.e3
ISSN
0015-0282 (ISSN-L)
OpenAlex
W2296497816
Cited by
15
References
37
Citations by year
2025: 2 · 2024: 2 · 2023: 1 · 2022: 3 · 2020: 4 · 2019: 2 · 2017: 1
FWCI
0.99
Type
journal article
Language
en
Open access
Locations
  • Fertility and Sterility (publishedVersion)
  • PubMed (publishedVersion)
  • Edinburgh Research Explorer (University of Edinburgh) (submittedVersion, cc-by-nd)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Ectopic Pregnancy Diagnosis and Management
  • Life Sciences › Immunology and Microbiology › Immunology › Reproductive System and Pregnancy
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Reproductive Health and Contraception
Keywords
gonadotropin-releasing hormone, GnRH receptor, tubal pregnancy, trophoblast, syncytiotrophoblast, cytotrophoblast, extravillous trophoblast, fallopian tube epithelium, GnRH signaling, GnRH antagonist, BeWo cells, HTR-8/SVneo cells
MeSH terms
Cell Line, Transformed, Cell Survival, Fallopian Tubes, Female, Humans, Gonadotropin-Releasing Hormone, Embryo Implantation, Pregnancy, Pregnancy, Tubal, Receptors, LHRH, Trophoblasts, Gene Expression Regulation, Developmental, Cell Line, Tumor

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