PMID- 17678915 OWN - NLM STAT- MEDLINE DCOM- 20080310 LR - 20080215 IS - 1556-5653 (Electronic) IS - 0015-0282 (Linking) VI - 89 IP - 2 DP - 2008 Feb TI - Endometrial and peritoneal expression of aromatase, cytokines, and adhesion factors in women with endometriosis. PG - 301-10 AB - OBJECTIVE: To examine messenger (m) RNA expression of aromatase, cytokines, and adhesion factors in women with and without endometriosis. DESIGN: Patients with endometriosis were compared with control patients. SETTING: University Hospital Gasthuisberg, Leuven, Belgium. PATIENT(S): A total of 35 patients who had laparoscopic surgery during the luteal phase (n = 20) or the menstrual phase (n = 15) were selected for this study based on cycle phase and presence/absence of endometriosis. INTERVENTION(S): Tissues of endometrium and macroscopically normal peritoneum were collected during hysteroscopy and laparoscopic surgery, respectively, from 24 women with revised American Society for Reproductive Medicine stage (rASRM) stages I-II (n = 12) and III-IV (n = 12) endometriosis and 11 control patients with normal pelvic. Tissue samples were selected from a tissue bank, based on the phase of the cycle (menstrual or luteal) and the presence/absence of endometriosis. MAIN OUTCOME MEASURE(S): The mRNA levels of aromatase, vimentin, vascular cell adhesion molecule 1 (VCAM-1), alpha(V) and beta(3) integrins, interleukin (IL)-1 beta, regulated on activation normal T-cell expressed and secreted (RANTES), and monocyte chemotactic protein 1 (MCP-1) were evaluated using real-time reverse transcriptase polymerase chain reaction. RESULT(S): During menstrual phase, increased endometrial mRNA levels of alpha(V) integrin, combined alpha(V)beta(3) integrins, and increased peritoneal IL-1 beta mRNA levels--but decreased peritoneal MCP-1 mRNA levels--were observed in women with endometriosis compared with control subjects. During luteal phase, endometrial mRNA levels of IL-1 beta and RANTES were increased in women with endometriosis compared with control subjects. Endometrial aromatase mRNA expression was higher in women with endometriosis than in control subjects in combined phases. Women with endometriosis had increased peritoneal mRNA expression of RANTES and VCAM-1 during menstrual compared with luteal phase. CONCLUSION(S): Aberrant mRNA expression of aromatase, cytokines, and adhesion factors in endometrium and peritoneum suggests that both tissues are involved in the pathogenesis of endometriosis. FAU - Kyama, Cleophas M AU - Kyama CM AD - Leuven University Fertility Center, Department of Obstetrics and Gynecology, University Hospital Gasthuisberg, Leuven, Belgium. FAU - Overbergh, Lutgart AU - Overbergh L FAU - Mihalyi, Attila AU - Mihalyi A FAU - Meuleman, Christel AU - Meuleman C FAU - Mwenda, Jason M AU - Mwenda JM FAU - Mathieu, Chantal AU - Mathieu C FAU - D'Hooghe, Thomas M AU - D'Hooghe TM LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20070806 PL - United States TA - Fertil Steril JT - Fertility and sterility JID - 0372772 RN - 0 (Cell Adhesion Molecules) RN - 0 (Chemokine CCL5) RN - 0 (Cytokines) RN - 0 (Interleukin-1beta) RN - 0 (RNA, Messenger) RN - 0 (Receptors, CCR2) RN - 0 (Vascular Cell Adhesion Molecule-1) RN - 0 (Vimentin) RN - EC 1.14.14.1 (Aromatase) SB - IM MH - Adult MH - Aromatase/*genetics/metabolism MH - Cell Adhesion Molecules/*genetics/metabolism MH - Chemokine CCL5/genetics/metabolism MH - Cytokines/*genetics/metabolism MH - Endometriosis/*genetics/metabolism MH - Endometrium/*metabolism MH - Female MH - Humans MH - Interleukin-1beta/genetics/metabolism MH - Luteal Phase/genetics/metabolism MH - Menstruation/genetics/metabolism MH - Peritoneum/*metabolism MH - RNA, Messenger/metabolism MH - Receptors, CCR2/genetics/metabolism MH - Uterine Diseases/*genetics/metabolism MH - Vascular Cell Adhesion Molecule-1/genetics/metabolism MH - Vimentin/genetics/metabolism EDAT- 2007/08/07 09:00 MHDA- 2008/03/11 09:00 CRDT- 2007/08/07 09:00 PHST- 2006/11/17 00:00 [received] PHST- 2007/02/27 00:00 [revised] PHST- 2007/02/27 00:00 [accepted] PHST- 2007/08/07 09:00 [pubmed] PHST- 2008/03/11 09:00 [medline] PHST- 2007/08/07 09:00 [entrez] AID - S0015-0282(07)00525-0 [pii] AID - 10.1016/j.fertnstert.2007.02.057 [doi] PST - ppublish SO - Fertil Steril. 2008 Feb;89(2):301-10. doi: 10.1016/j.fertnstert.2007.02.057. Epub 2007 Aug 6.