Volume 16, Issue 9 (September 2018)                   IJRM 2018, 16(9): 549-556 | Back to browse issues page

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Golestan Jahromi M, Aflatoonian R, Afsharian P, Aghajanpour S, Shahhoseini M, Aflatoonian A. Altered expression of 3´paralogus HOX A-D clusters in endometriosis disease: A case-control study. IJRM 2018; 16 (9) :549-556
URL: http://ijrm.ir/article-1-1238-en.html
Altered expression of 3´paralogus HOX A-D clusters in endometriosis disease: A case-control study
Masoumeh Golestan Jahromi1 , Reza Aflatoonian2 , Parvaneh Afsharian3 , Samaneh Aghajanpour2 , Maryam Shahhoseini3 , Abbas Aflatoonian * 4
1- Research and Clinical Center for Infertility, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
2- Department of Endocrinology and Female Infertility, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
3- Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran
4- Research and Clinical Center for Infertility, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran , abbas_aflatoonian@yahoo.com
Abstract:   (3289 Views)

Background: Endometriosis is a prevalent gynecological disease, with limited known etiology and more researches are required to identify its etiology. In this manner, there is no evidence for expression and function of 3´HOX genes in 4 clusters in the limb and pelvic organs such as the uterus and its disorders (Genes in the HOXA-D clusters are subdivided into 13 paralogous groups).
Objective: This study designed to investigate the expression profile of 5 paralogous (1-5) in four clusters of HOX genes (A, B, C, and D) in ectopic and eutopic tissues of women with endometriosis compared to the normal endometrium.
Materials and Methods: Samples were obtained from thirty patients (15 with and 15 without endometriosis) of reproductive age with normal menstrual cycles. The same patient provided both eutopic and ectopic tissues and control women were laparoscopically checked for the absence of endometriosis. The expression profile of these HOX genes was investigated by quantitative real-time polymerase chain reaction technique.
Results: We observed significant up-regulation of some members of HOXC and D clusters (HOXD1, HOXD3, HOXC4 and HOXC5) in ectopic and eutopic tissues vs. control. Also, our data showed significant down-regulation of all of HOXA and HOXB paralogous except HOXA1 in ectopic tissues versus control.
Conclusion: Our data showed specific cluster dependent modulation of the HOX genes expression in endometriosis (over-expression of some HOX genes in cluster C and D and down-regulation of HOX genes in cluster A and B) in ectopic and eutopic tissues compare to control group. Therefore, it is possible that change of expression level of these genes in endometrium plays a role in the pathogenesis of endometriosis.
Keywords: Endometriosis, HOX genes, Eutopic endometrium, Ectopic endometrium
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Type of Study: Original Article | Subject: Assisted Reproductive Technologies
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