Literature DB >> 12917785

Matrix metalloproteinases and endometriosis.

Kevin G Osteen1, Grant R Yeaman, Kaylon L Bruner-Tran.   

Abstract

Retrograde menstruation represents a plausible explanation for the development of most cases of endometriosis; nevertheless, additional factors must contribute to the development of disease in only 10 to 20% of women. The discriminating factor(s) in determining the development of active endometriosis probably involves a complex array of potentially interactive influences including steroid exposure, immunological disturbances, genetic predisposition, and, perhaps, environmental toxin exposure. Matrix metalloproteinases (MMPs), enzymes that mediate normal tissue turnover including endometrial breakdown at menstruation, appear to be involved in the invasive establishment of the disease. In addition, several MMPs appear to be inappropriately expressed in the endometrium of women with this disease in association with a reduced sensitivity to progesterone. Altered regulation of endometrial MMP expression in response to steroids may represent a mechanism linking the invasive potential of refluxed endometrium to the establishment of this disease only in certain women.

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Year:  2003        PMID: 12917785     DOI: 10.1055/s-2003-41322

Source DB:  PubMed          Journal:  Semin Reprod Med        ISSN: 1526-4564            Impact factor:   1.303


  39 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.  EMMPRIN is secreted by human uterine epithelial cells in microvesicles and stimulates metalloproteinase production by human uterine fibroblast cells.

Authors:  A G Braundmeier; C A Dayger; P Mehrotra; R J Belton; R A Nowak
Journal:  Reprod Sci       Date:  2012-06-22       Impact factor: 3.060

Review 3.  Dioxin may promote inflammation-related development of endometriosis.

Authors:  Kaylon L Bruner-Tran; Grant R Yeaman; Marta A Crispens; Toshio M Igarashi; Kevin G Osteen
Journal:  Fertil Steril       Date:  2008-04-18       Impact factor: 7.329

4.  Association between matrix metalloproteinase-2 and matrix metalloproteinase-9 polymorphisms and endometriosis: A systematic review and meta-analysis.

Authors:  Lingli Xin; Qingxiang Hou; Q I Xiong; Xiaoping Ding
Journal:  Biomed Rep       Date:  2015-04-06

Review 5.  Novel therapies targeting endometriosis.

Authors:  Hugh S Taylor; Kevin G Osteen; Kaylon L Bruner-Tran; Charles J Lockwood; Graciela Krikun; Anna Sokalska; Antoni J Duleba
Journal:  Reprod Sci       Date:  2011-06-21       Impact factor: 3.060

6.  Coding regions of INHBA, SFRP4 and HOXA10 are not implicated in familial endometriosis linked to chromosome 7p13-15.

Authors:  J Lin; L Zong; S H Kennedy; K T Zondervan
Journal:  Mol Hum Reprod       Date:  2011-05-16       Impact factor: 4.025

7.  Adenoviral vector encoding soluble Flt-1 engineered human endometrial mesenchymal stem cells effectively regress endometriotic lesions in NOD/SCID mice.

Authors:  A R Koippallil Gopalakrishnan; H Pandit; S M Metkari; N Warty; T Madan
Journal:  Gene Ther       Date:  2016-03-18       Impact factor: 5.250

8.  TIMP1 contributes to ovarian anomalies in both an MMP-dependent and -independent manner in a rat model.

Authors:  Julie A W Stilley; Kathy L Sharpe-Timms
Journal:  Biol Reprod       Date:  2012-02-29       Impact factor: 4.285

9.  Abnormal regulation of chemokine TECK and its receptor CCR9 in the endometriotic milieu is involved in pathogenesis of endometriosis by way of enhancing invasiveness of endometrial stromal cells.

Authors:  Yun Wang; Jing Yu; Xuezhen Luo; Xiaoqiu Wang; Mingqing Li; Ling Wang; Dajin Li
Journal:  Cell Mol Immunol       Date:  2010-01       Impact factor: 11.530

10.  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

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