Literature DB >> 18722604

Induction of peritoneal endometriosis in nude mice with use of human immortalized endometriosis epithelial and stromal cells: a potential experimental tool to study molecular pathogenesis of endometriosis in humans.

Sakhila K Banu1, Anna Starzinski-Powitz, V O Speights, Robert C Burghardt, Joe A Arosh.   

Abstract

OBJECTIVE: To determine whether a mixed population of immortalized human endometriosis epithelial and stromal cells is able to induce peritoneal endometriosis in nude mice.
DESIGN: Prospective experimental study. Human immortalized endometriosis epithelial and stromal cells were xenografted into ovariectomized nude mice. Macroscopically, the number of induced endometriosis-like lesions and their color were determined. Microscopically, histomorphology of endometriosis glands and their structure were analyzed, and comparisons were made with tissue from spontaneous endometriosis in women.
SETTING: College of Veterinary Medicine and Biomedical Sciences, Texas A&M University. ANIMALS: Seven ovariectomized nude mice. INTERVENTION(S): Minimal invasive procedures were performed to administer estrogen pellets and transplant immortalized human endometriosis epithelial and stromal cells into nude mice. MAIN OUTCOME MEASURE(S): Peritoneal endometriosis-like lesions induced in nude mice were characterized and compared with spontaneous peritoneal endometriosis in women. RESULT(S): Xenografts of human immortalized endometriosis epithelial and stromal cells into the peritoneal cavity of the recipient nude mice are able to proliferate, attach, invade, reorganize, and establish peritoneal endometriosis. Endometriosis glands at different stages of growth were present in induced endometriosis-like lesions. Proliferating cell nuclear antigen, metalloproteinase 2, estrogen receptor-alpha, cyclooxygenase-2, and prostaglandin E(2) receptors EP2 and EP4 proteins were expressed in both endometriosis glandular epithelial and stromal cells of the induced endometriosis-like lesions. CONCLUSION(S): This xenograft model could be used as a potential experimental tool to understand the molecular and cellular aspects of the pathogenesis of endometriosis in humans.

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Year:  2008        PMID: 18722604     DOI: 10.1016/j.fertnstert.2008.06.050

Source DB:  PubMed          Journal:  Fertil Steril        ISSN: 0015-0282            Impact factor:   7.329


  11 in total

1.  A new isoform of steroid receptor coactivator-1 is crucial for pathogenic progression of endometriosis.

Authors:  Sang Jun Han; Shannon M Hawkins; Khurshida Begum; Sung Yun Jung; Ertug Kovanci; Jun Qin; John P Lydon; Francesco J DeMayo; Bert W O'Malley
Journal:  Nat Med       Date:  2012-07       Impact factor: 53.440

2.  Activated glucocorticoid and eicosanoid pathways in endometriosis.

Authors:  Diana Monsivais; Jeffrey D Bray; Emily Su; Mary Ellen Pavone; Matthew T Dyson; Antonia Navarro; Toshiyuki Kakinuma; Serdar E Bulun
Journal:  Fertil Steril       Date:  2012-04-21       Impact factor: 7.329

3.  Molecular and preclinical basis to inhibit PGE2 receptors EP2 and EP4 as a novel nonsteroidal therapy for endometriosis.

Authors:  Joe A Arosh; JeHoon Lee; Dakshnapriya Balasubbramanian; Jone A Stanley; Charles R Long; Mary W Meagher; Kevin G Osteen; Kaylon L Bruner-Tran; Robert C Burghardt; Anna Starzinski-Powitz; Sakhila K Banu
Journal:  Proc Natl Acad Sci U S A       Date:  2015-07-21       Impact factor: 11.205

4.  A novel nude mouse model for studying the pathogenesis of endometriosis.

Authors:  Li-Ping Li; Zeng-Ming Li; Zhao-Zhen Wang; Yu-Fen Cheng; De-Ming He; Ge Chen; Bian-Na Cao; Yang Zou; Yong Luo
Journal:  Exp Ther Med       Date:  2022-06-08       Impact factor: 2.751

5.  Selective inhibition of prostaglandin E2 receptors EP2 and EP4 inhibits adhesion of human endometriotic epithelial and stromal cells through suppression of integrin-mediated mechanisms.

Authors:  JeHoon Lee; Sakhila K Banu; Robert C Burghardt; Anna Starzinski-Powitz; Joe A Arosh
Journal:  Biol Reprod       Date:  2013-03-28       Impact factor: 4.285

6.  Selective inhibition of prostaglandin E2 receptors EP2 and EP4 induces apoptosis of human endometriotic cells through suppression of ERK1/2, AKT, NFkappaB, and beta-catenin pathways and activation of intrinsic apoptotic mechanisms.

Authors:  Sakhila K Banu; JeHoon Lee; V O Speights; Anna Starzinski-Powitz; Joe A Arosh
Journal:  Mol Endocrinol       Date:  2009-04-30

7.  PPARγ activation inhibits growth and survival of human endometriotic cells by suppressing estrogen biosynthesis and PGE2 signaling.

Authors:  Dan I Lebovic; Shahryar K Kavoussi; JeHoon Lee; Sakhila K Banu; Joe A Arosh
Journal:  Endocrinology       Date:  2013-09-24       Impact factor: 4.736

8.  Enzymes of the AKR1B and AKR1C Subfamilies and Uterine Diseases.

Authors:  Tea Lanišnik Rižner
Journal:  Front Pharmacol       Date:  2012-03-13       Impact factor: 5.810

9.  Novel three-dimensional in vitro models of ovarian endometriosis.

Authors:  Doerthe Brueggmann; Claire Templeman; Anna Starzinski-Powitz; Nagesh P Rao; Simon A Gayther; Kate Lawrenson
Journal:  J Ovarian Res       Date:  2014-02-06       Impact factor: 4.234

Review 10.  Relevant human tissue resources and laboratory models for use in endometriosis research.

Authors:  Erin Greaves; Hilary O D Critchley; Andrew W Horne; Philippa T K Saunders
Journal:  Acta Obstet Gynecol Scand       Date:  2017-04-05       Impact factor: 3.636

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