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NF-κB、COX-2在子宫腺肌病中的表达及意义

The expression and significance of NF-κB and COX-2 in uterine adenomyosis
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摘要 目的 探讨核因子κB(NF-κB)、环氧化酶-2(COX-2)在子宫腺肌病中的表达及意义.方法 应用免疫组化法检测NF-κB、COX-2在正常子宫内膜(对照组)、子宫腺肌病在位子宫内膜(在位内膜组)、异位子宫内膜(异位内膜组)中的表达.结果 NF-κB在子宫腺肌病异位内膜组和在位内膜组的表达均明显高于对照组(P<0.05),异位内膜组的表达明显高于在位内膜组(P<0.05);COX-2在子宫腺肌病异位内膜组和在位内膜组的表达均明显高于对照组(P<0.05),异位内膜组的表达明显高于在位内膜组(P<0.05).NF-κB、COX-2在子宫腺肌病异位内膜中的表达呈正相关(r=0.786,P<0.05).结论 NF-κB、COX-2在子宫腺肌病的发生发展过程中可能发挥重要作用. Objective To investigate the expression and significance of nuclear factor κB ( NF - κB) and cyclooxy- genase - 2 ( COX - 2 ) in uterine adenomyosis. Methods The expression of NF - κB and COX - 2 was examined by immnnohistochemical detection of substance P (SP) in normal endometrium (control group), eutopic endometrium (eutopic group) and eetopie endometrium (eetopic group). Results NF -κB expression in ectopic group and eutopic group was significantly higher than that in normal group ( P 〈 0.05 ), and NF - κB expression in ectopie group was significantly higher than that in eutopic group ( P 〈 0.05 ) ; COX - 2 expression in ectopic group and eutopic group was significantly higher than that in normal group ( P 〈 0.05 ) , and COX - 2 expression in ectopic group was significantly higher than that in eutopic group (P 〈 0.05 ). There was a positive correlation between NF -κB expression and COX - 2 expression in ectopic endometrium in uterine adenomyosis (r = 0.786, P 〈 0. 05). Conclusion NF - κB and COX - 2 may play important roles in the pathogenesis and progression of uterine adenomyosis,
作者 李明 陆晓媛
出处 《徐州医学院学报》 CAS 2011年第2期102-104,共3页 Acta Academiae Medicinae Xuzhou
关键词 子宫腺肌病 核因子ΚB 环氧化酶-2 免疫组织化学 uterine adenomyosis nuclear factor KB cyclooxygenase - 2 immunohistochemistry
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  • 1Kim MD, Won JW, Lee DY, adenomyosis without fibroids et al. Uterine artery embolization for [ J]. Clin Radiol, 2004, 59 (6) : 520 -526.
  • 2Jang BC, Kim DH, Park JW, et al. Induction of cyclooxygenase - 2 in macrophages by catalase: role of NF - KB and PI3K signaling pathways [J]. Biochem Biophy Res Commun, 2004,326(2): 398 -406.
  • 3Kempe S, Kestler H, Lasar A, et al. NF - KB controls the global proinflammatory response in endothelial cells: evidence for the regulation of a pro -atherogenic program [ J]. Nucleic Acids Res, 2005, 33(16) :5308 -5319.
  • 4Ota H, Igarashi S, Sasaki M, et al. Distribution of cyclooxygenase -2 in eutopic and ectopic endometrium in endometriosis and adenomyosis [J]. Human Reprod, 2001, 16(3) :561 -566.
  • 5Adelizzi RA. COX- 1 and COX-2 in health and disease [J]. J Am Osteopath Assoc, 1999, 99( 11 Suppl) :s7 -S12.
  • 6Seiberl K, Masferrer JL. Role of inducible cyclooxygenase ( COX - 2) in inflanlmation [ J]. Receptor, 1994, 4 ( 1 ) : 17 - 23.
  • 7Bulun SE, Yang S, Fang Z, et al. Estrogen production and metabolism in endometriosis [ J]. Ann N Y Acad Sci, 2002, 955:75 -85.
  • 8Appleby SB, Ristimaki A, Neilson K, et al. Structure of the hu- man cyclo - oxygenase - 2 gene [ J]. Biochem J, 1994, 302 ( Pt 3) :723 -727.

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