Evaluation of Endometrial Stromal Cell Apoptosis in Adenomyosis
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|ClinicalTrials.gov Identifier: NCT00172588|
Recruitment Status : Unknown
Verified December 2004 by National Taiwan University Hospital.
Recruitment status was: Recruiting
First Posted : September 15, 2005
Last Update Posted : November 28, 2005
Our previous results revealed that the expression of killer inhibitory receptors (KIRs) on NK cells was decreased in eutopic endometrium in women with adenomyosis. It implies that the formation of adenomyosis might be due to abnormal endometrial tissues, but not the aberrant local immunological dysfunction in myometrium. In addition, in vitro coculture of macrophages and endometrial stromal cells (ESC) increase the expression of IL-6 mRNA in ESC, which might further enhance the proliferation of ESC and subsequently result in the formation of ectopic endometrial implants in adenomyosis. Besides, another possible mechanism is the abnormal apoptosis of ESC in adenomyosis. In endometriosis, apoptotic endometrial cells were found to be decreased, which possibly accounts for the formation of endometriosis. However, there have not been reports investigating the apoptosis of ESC in adenomyosis.
In this study, we try to investigate apoptotic ESC with flow cytometry in women with and without adenomyosis. Annexin V, bcl-2, and caspase-3 were measured to represent the degree of apoptosis in ESC.
|Condition or disease|
Eutopic endometrium was obtained and separated into single endometrial stromal cell (ESC) in women with adenomyosis (study group) and without adenomyosis (control group).
Annexin V-PE, bcl-2-PE, and caspase-3-PE are stained, and flow cytometry is done to measure the degree of apoptosis in ESC. On the other hand, another half of ESC are cultured for 24h, and also Annexin V-PE, bcl-2-PE, and caspase-3-PE are stained, and flow cytometry is done.
|Study Type :||Observational|
|Enrollment :||40 participants|
|Observational Model:||Defined Population|
|Observational Model:||Natural History|
|Study Start Date :||January 2005|
|Study Completion Date :||October 2005|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00172588
|Contact: Jehn-Hsiahn Yang, M.D.||886-2-2312-3456 ext email@example.com|
|National Taiwan University Hospital||Recruiting|
|Contact: Jehn-Hsiahn Yang, M.D. 886-2-2312-3456 ext 3210 firstname.lastname@example.org|
|Principal Investigator: Jehn-Hsiahn Yang, M.D.|
|Principal Investigator:||Jehn-Hsiahn Yang, M.D.||Department of Obstetrics and Gynecology, National Taiwan University Hospital|