Endometriosis Knowledgebase


A repository for genes associated with endometriosis

Results


PMID 20171623
Gene Name HOXA10
Condition Endometriosis (Peritoneal)
Association Associated
Population size 71
Population details 71 (30 deep endometriotic nodules, 11 peritoneal lesions, 30 eutopic endometrium and vaginal tissue (n=30) were collected for control purposes)
Sex Female
Associated genes HOXA-9, HOXA-10, HOXA-11, and HOXA-13
Other associated phenotypes Peritoneal endometrisis
Differential expression of genes from the homeobox A cluster in deep endometriotic nodules and peritoneal lesions.

Fertil Steril. 2010 Nov;94(6):1995-2000. doi: 10.1016/j.fertnstert.2010.01.003.

Van Langendonckt, Anne| Luyckx, Mathieu| Gonzalez, Maria-Dolores| Defrere, Sylvie| Donnez, Jacques| Squifflet, Jean

Department of Gynecology, Universite Catholique de Louvain, 1200 Brussels, Belgium.

OBJECTIVE: To compare expression of homeobox A (HOXA) genes involved in the differentiation of the female reproductive tract in deep endometriotic nodules and peritoneal lesions. DESIGN: Prospective experimental study. SETTING: Academic gynecology research unit. PATIENT(S): Thirty patients undergoing laparoscopy. INTERVENTION(S): During laparoscopy, deep endometriotic nodules (n=30) and peritoneal lesions (n=11) were recovered. Eutopic endometrium and vaginal tissue (n=30) were collected for control purposes. MAIN OUTCOME MEASURE(S): Quantification of HOXA-9, HOXA-10, HOXA-11, and HOXA-13 in deep nodules, peritoneal lesions, and control samples by real-time reverse-transcription polymerase chain reaction, and localization of HOXA-10 and HOXA-13 proteins by immunohistochemistry. RESULT(S): The HOXA-13 transcripts were detected in 29 out of 30 nodules, and their expression was significantly higher than in vaginal tissue, but they were barely detectable in endometrium and peritoneal lesions. Expression of HOXA-10 and HOXA-11 transcripts in deep nodules was similar to eutopic endometrium, and HOXA-10 expression was significantly lower in peritoneal endometriotic lesions. The HOXA-10 immunostaining was mainly localized in the stroma of deep endometriotic nodules, HOXA-13 in glandular structures and stroma, and neither of these proteins were detected in fibromuscular areas. CONCLUSION(S): Marked expression of HOXA-10 and HOXA-13 in the endometrium-like tissue of nodules but low expression in peritoneal endometriotic lesions supports the theory of differential origin of these two types of endometriosis.

Mesh Terms: Adult| Endometriosis/*genetics/metabolism/pathology| Female| Gene Expression Profiling| *Gene Expression Regulation/physiology| Genes, Homeobox/*genetics| Homeodomain Proteins/analysis/genetics/metabolism| Humans| Immunohistochemistry| Multigene