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宫颈癌组织中环氧合酶-2表达及其与血管生成和细胞增殖的关系 被引量:2

Expression of Cyclooxygenase-2 and its Relationship with Neovascularization and Tumor Cell Proliferation in Cervical Carcinoma
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摘要 目的 探讨宫颈癌组织中环氧合酶 2 (COX 2 )表达及其与血管生成和细胞增殖的关系。方法 采用免疫组织化学S P法检测 41例宫颈癌和 10例正常宫颈上皮组织中COX 2表达 ,并检测其微血管密度 (CD3 4标记 )和癌细胞增殖指数 (Ki 67标记 )。结果 宫颈癌组织中COX 2、微血管密度、Ki 67指数明显高于正常宫颈上皮组织 (P <0 .0 1) ,COX 2高表达与宫颈癌淋巴结转移和浸润深度有关 (P <0 .0 5 ) ,与患者年龄、临床分期、组织学类型、分化程度无关 (P >0 .0 5 ) ,COX 2表达阳性者微血管密度和Ki 67指数明显高于COX 2表达阴性者 (P <0 .0 5 )。结论 COX 2过度表达可能参与宫颈癌的发生发展 ,且与宫颈癌新生血管的形成和细胞增殖有密切关系 。 Objective To investigate the expression of COX-2 and its relationship with neovascularization and tumor cell proliferation in cervical carcinoma.Methods The expression of COX-2,microvascular density(MVD)labelled by CD34 protein and proliferation indexes of cancer cells labelled by Ki-67 protein were examined by immunohistochemistry S-P method in 41 cases of cervical carcinomas and 10 cases of normal cervical epithelium.Results The expression of COX-2、MVD、Ki-67 indexes was significantly higher in cervical carcinomas than in normal cervical epithelia(P<0.01).Overexpression of COX-2 in cervical carcinomas was related to lymph node metastasis and depth of invasion,but had no relation to age,FIGO staging,histopathological type and differentiation degree(P>0.05).The MVD and Ki-67 indexes were significantly higher in the COX-2-positive tumors than in the negative ones(P<0.05).Conclusion The expression of COX-2 may play an important role in carcinogenesis and development of cervical carcinoma.It is also closely related with neovascularization and tumor cell proliferation.Detection of COX-2 protein may be valuable to further understand the biological behavior of cervical carcinoma.
出处 《实用癌症杂志》 2004年第2期151-154,共4页 The Practical Journal of Cancer
关键词 宫颈癌 癌组织 环氧合酶-2 血管生成 细胞增殖 肿瘤转移 免疫组织化学S-P法 Cervical carcinoma Cyclooxygenase-2(COX-2) Microvascular density(MVD) Ki-67 Immunohistochemistry
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  • 1Ferrandina G,Lauriola L,Distefano MG,et al. Increased cyclooxygenase-2 expression is associated with chemotherapy resistance and poor survival in cervical cancer patients[J]. J Clin Oncol, 2002,20(4) :973.
  • 2Dannenberg AJ, Altorki NK, Boyle JO, et al. Cyclo-oxygenase 2: a pharmacological target for the prevention of cancer [J ]. Lancet Oncol, 2001,2 (9): 544.
  • 3Dempke W,Rie C,Grothey A,et al. Cyclooxygenase-2:a novel target for cancer chemotherapy.? [J ]. J Cancer Res Clin Oncol, 2001,127(7) :411.
  • 4Ryu HS,Chang KH,Yang HW,et al. High cyclooxygenase-2 expression in stage IB cervical cancer with lymphnode metastasis or parametrial invasion[J ]. Gynecol Oncol, 2000,76 (3): 320.
  • 5Kim MH, Seo SS, Song YS, et al. Expression of cyclooxygenase-1 and -2 associated with expression of VEGF in primary cervical cancer and at metastatic lymph nodes[J ]. Gynecol Oncol,2003,90(1): 83.
  • 6Chen YJ, Wang LS, Wang PH, et al. High cyclooxygenase-2 expression in cervical adenocarcinomas [J ]. Gynecol Oncol, 2003,88 (3): 379.
  • 7Folkman J. Angiogenesis and angiogenesis inhibition:an overview[J ]. EXS, 1997,79:1.
  • 8Hamada L, Cavanaugh PG, Lotan O, et al. Separable growth and migration factors for large-cell lymphoma cells secreted by microvascular endothelial cells derived from target organs for metastasis[J ]. Br J Cancer, 1992,66(2): 349.
  • 9Fosslien E. Review: molecular pathology of cyclooxygenase-2 in cancer-induced angiogenesis[J ]. Ann Clin Lab Sci,2001,31 (4) :325.
  • 10Shariat SF,Matsumoto K, Kim J,et al. Correlation of cyclooxygenase-2 expression with molecular markers,pathological features and clinical outcome of transitional cell carcinoma of the bladder [J ]. J Urol, 2003, 170 (3):985.

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