浙江医学
浙江醫學
절강의학
ZHEJIANG MEDICAL JOURNAL
2014年
17期
1457-1459,1471
,共4页
王建芳%范伟荣%刘杰%伊碧霞%章根琴
王建芳%範偉榮%劉傑%伊碧霞%章根琴
왕건방%범위영%류걸%이벽하%장근금
子宫内膜异位症%脂氧素A4%脂氧素A4受体ALXR%炎症
子宮內膜異位癥%脂氧素A4%脂氧素A4受體ALXR%炎癥
자궁내막이위증%지양소A4%지양소A4수체ALXR%염증
Endometriosis%Lipoxin A4%Lipoxin A4 receptor ALXR%Inflammation
目的:探讨脂氧素A4受体ALXR在子宫内膜异位症(EMs)患者在位及异位内膜组织中的表达水平及其临床意义。方法因EMs行腹腔镜手术治疗的患者27例,留取在位子宫内膜组织(EMs在位内膜组)和异位子宫内膜组织(EMs异位内膜组),取同期因良性卵巢囊肿行腹腔镜手术治疗患者30例为对照组,留取宫腔内正常内膜组织。分别采用实时荧光定量PCR技术、免疫组化法检测各组内膜组织中ALXR mRNA及蛋白表达水平。结果 EMs异位内膜组ALXR mRNA表达水平为0.069±0.020,EMs在位内膜组为0.039±0.013,对照组为0.019±0.008,EMs异位和在位内膜组的表达水平均明显高于对照组(均P<0.05),EMs异位内膜组又高于在位内膜组(P<0.05)。EMs异位和在位内膜组ALXR蛋白表达水平明显高于对照组(P<0.05)。结论 ALXR mRNA及蛋白在EMs异位及在位内膜组织中均呈高表达状态,推测ALXR可能与EMs发病有关。
目的:探討脂氧素A4受體ALXR在子宮內膜異位癥(EMs)患者在位及異位內膜組織中的錶達水平及其臨床意義。方法因EMs行腹腔鏡手術治療的患者27例,留取在位子宮內膜組織(EMs在位內膜組)和異位子宮內膜組織(EMs異位內膜組),取同期因良性卵巢囊腫行腹腔鏡手術治療患者30例為對照組,留取宮腔內正常內膜組織。分彆採用實時熒光定量PCR技術、免疫組化法檢測各組內膜組織中ALXR mRNA及蛋白錶達水平。結果 EMs異位內膜組ALXR mRNA錶達水平為0.069±0.020,EMs在位內膜組為0.039±0.013,對照組為0.019±0.008,EMs異位和在位內膜組的錶達水平均明顯高于對照組(均P<0.05),EMs異位內膜組又高于在位內膜組(P<0.05)。EMs異位和在位內膜組ALXR蛋白錶達水平明顯高于對照組(P<0.05)。結論 ALXR mRNA及蛋白在EMs異位及在位內膜組織中均呈高錶達狀態,推測ALXR可能與EMs髮病有關。
목적:탐토지양소A4수체ALXR재자궁내막이위증(EMs)환자재위급이위내막조직중적표체수평급기림상의의。방법인EMs행복강경수술치료적환자27례,류취재위자궁내막조직(EMs재위내막조)화이위자궁내막조직(EMs이위내막조),취동기인량성란소낭종행복강경수술치료환자30례위대조조,류취궁강내정상내막조직。분별채용실시형광정량PCR기술、면역조화법검측각조내막조직중ALXR mRNA급단백표체수평。결과 EMs이위내막조ALXR mRNA표체수평위0.069±0.020,EMs재위내막조위0.039±0.013,대조조위0.019±0.008,EMs이위화재위내막조적표체수평균명현고우대조조(균P<0.05),EMs이위내막조우고우재위내막조(P<0.05)。EMs이위화재위내막조ALXR단백표체수평명현고우대조조(P<0.05)。결론 ALXR mRNA급단백재EMs이위급재위내막조직중균정고표체상태,추측ALXR가능여EMs발병유관。
Objective To investigate the expression of lipoxin A4 receptor (ALXR) in eutopic and ectopic endometrium of patients with endometriosis. Methods Twenty seven patients with endometriosis underwent laparoscopic surgery in our hospital between February 2012 and September 2012, the tissue samples of eutopic and ectopic endometrium were col ected;and uterine endometrium samples were also col ected from 30 patients with benign ovary cysts as controls. The mRNA and protein expression of ALXR in the eutopic endometrium, ectopic endometrium of endometriosis patients and control endometri-um were detected by real- time fluorescent quantitative RT- PCR and immunohistochemistry, respectively. Results The mRNA expression of ALXR was 0.069 ±0.013 in ectopic endometrium and 0.039 ±0.013 in eutopic endometrium of endometriosis, which were significantly higher than that of the control (0.019±0.008, P<0.05). The mRNA expression of ALXR in the ectopic endometrium was also higher than that of eutopic endometrium of endometriosis (P<0.05). Compared with the control, the ex-pression of ALXR protein in eutopic and ectopic endometrium of endometriosis were increased (P<0.05). Conclusion The ec-topic and eutopic endometrium in patients with endometriosis shows high expression of lipoxin A4 receptor mRNA and protein, which indicates that ALXR may be associated with the pathogenesis of endometriosis.