期刊文献+

基质金属蛋白酶组织抑制物-1在宫颈癌的表达与临床意义 被引量:9

Expression of Tissue Inhibitor of Metalloproteinase-1 and Its Clinical Significance in Invasive Carcinoma of Cervix
下载PDF
导出
摘要 目的 :探讨基质金属蛋白酶组织抑制物 - 1(TIMP- 1)在早期宫颈癌的表达和临床意义。方法 :采用免疫组织化学 SP法检测 75例早期宫颈浸润癌 (宫颈癌组 )、18例宫颈上皮内瘤样病变 (CIN组 )和 15例癌旁正常宫颈上皮 (对照组 )中 TIMP- 1的表达情况 ,并检测其中微血管密度 (CD34 标记 )和癌细胞增殖标记指数 (Ki- 6 7标记 )。结果 :TIMP- 1主要表达于宫颈癌细胞膜和 (或 )细胞浆 ,Ki- 6 7主要表达于癌细胞核 ,CD34 主要表达于癌巢间质血管内皮细胞。从对照组到 CIN组再到宫颈癌组 ,TIMP- 1的阳性表达率未见显著升高 (P>0 .0 5 )。 TIMP- 1在宫颈癌中表达与 FIGO分期、组织学分级、盆腔淋巴结转移和间质浸润深度有关 (P<0 .0 5 ) ;而与年龄、组织学类型、脉管浸润、Ki- 6 7表达及微血管密度无关 (P>0 .0 5 )。 FIGO分期为 期、组织学分级为 级、有盆腔淋巴结转移及突破深肌层间质浸润者 ,其 TIMP- 1阳性表达率分别显著低于 FIGO分期为 期、组织学分级在 级以内、无盆腔淋巴结转移和浸润深度在浅肌层间质以内者 (P<0 .0 5 )。结论 :宫颈癌 TIMP- 1表达降低可能在侵袭转移中起一定作用。检测宫颈癌 TIMP- 1表达对进一步了解宫颈癌生物学行为和判断预后有一定价值。 Objective:Expression and clinical significance of tissue inhibitor of metalloproteinase-1 (TIMP-1) in early invasive carcinoma of cervix were investigated to explore its clinical significance.Methods:The expression of TIMP-1, microvessel density labeled by CD 34and proliferation index of cancer cells labeled by Ki-67 in 75 cases of early invasive carcinoma of cervix (ICC group), 18 cases of cervical intraepithelial neoplasm (CIN group) and 15 cases of normal cervical epithelium (control group) remote from tumor were detected by immunohistochemistry SP method.Results:TIMP-1 was mainly expressed in the cellular membrane and/or cytoplasm in tumor cells, whereas expression of Ki-67 was mainly confined to the nuclei, and that of CD 34 to the vascular epithelial cells in tumor stroma. The positive rates of expression of TIMP-1 did not increase remarkably from control to CIN, and then to ICC group (P>0.05). In ICC group, the expression of TIMP-1 correlated with FIGO staging, histological grading, pelvic lymph node metastasis and stroma infiltration (P<0.05), but not correlated with patients age, histological types, intravascular infiltration, Ki-67 expression and microvessel density (P>0.05). In the cases with FIGO staging Ⅱ, histological grading Ⅲ, pelvic lymph node metastasis and deeper stroma infiltration, the positive rate of expression of TIMP-1 was significantly lower than that in those without the conditions mentioned above (P<0.05).Conclusion:Lower expression of TIMP-1 may play an important role during cancer invasion and metastasis in invasive carcinoma of cervix. Detection expression of TIMP-1 may be of value in further understanding the biological behavior and predicting the prognosis of cervical carcinoma.
出处 《中国误诊学杂志》 CAS 2003年第12期1767-1770,共4页 Chinese Journal of Misdiagnostics
基金 福建省教育厅科研基金资助项目 (项目编号0 1 B0 1 7)
关键词 宫颈肿瘤/病理学 宫颈肿瘤/血液供给 金属蛋白酶1组织抑制剂/代谢 淋巴转移 免疫组织化学 Cervix neoplasms/pathology Cervix neoplasms/blood supply Tissue inhibitor of metalloproteinase-1/metabolism Lymphatic metastasis Immunohistochemistry
  • 相关文献

参考文献9

  • 1[1]Kugler A. Matrix metalloproteinases and their inhibitors. Anticancer Res, 1999,19 (2C):1589-1592
  • 2江忠清,朱凤川,曲军英,郑秀,游彩玲.MMP-9和TIMP-1表达与宫颈癌细胞增殖及侵袭转移关系的研究[J].肿瘤防治杂志,2003,10(6):614-617. 被引量:4
  • 3江忠清,朱凤川,曲军英,郑秀,游彩玲.宫颈癌MMP-9表达与肿瘤血管生成、癌细胞增殖及侵袭转移的关系[J].癌症,2003,22(2):178-184. 被引量:55
  • 4[4]Massova I, Kotra LP, Fridman R, et al. Matrix metalloproteinases: structures,evolution and diversification. FASEB J, 1999, 12 (12):1075-1095
  • 5[5]Davidson B, Goldberg I, Kopolovic J, et al. Expression of metalloproteinase-9 in squamous cell carcinoma of the uterine cervix-clinicopathologic study using immunohistochemistry and mRNA in situ hybridization. Gynecol Oncol, 1999, 72 (3):380-386
  • 6[6]Kim I, Kim HG, Moon SO, et al. Angiopoietin-1 induces endothelial cell sprouting through the activation of focal adhesion kinase and plasmin secretion . Circ Res, 2000, 86 (9): 952-959
  • 7[7]Ray JM, Stetler-Stevenson WG. The role of matrix metalloproteinases and their inhibitor in tumour invasion, metastasis and angiogenesis. Eur Respir J, 1994,7(11): 2026-2072
  • 8[8]Yoshiji H, Harris SR, Rosa E, et al. Mammary carcinoma cells over-expressing tissue inhibitor of metalloproteinases-1 show enhanced vascular endothelial growth factor expression. Int J Cancer, 1998, 75 (1): 81-87
  • 9[9]Soloway PD, Alexander CM, Werb Z, et al. Targeted mutagenesis of TIMP-1 reveals that lung tumor invasion is influenced by TIMP-1 genotype of the tumor but not by that of host.Oncogene, 1996, 13 (11): 2307

二级参考文献22

  • 1[1]Kugler A.Matrix metalloproteinases and their inhibitors[J].Anticancer Res,1999,19(2C):1589-1592.
  • 2[2]Davidson B,Goldberg I,Kopolovic J,et al.Expression of metalloproteinase-9 in squamous cell carcinoma of the uterine cervix-clinicopathologic study using immunohistochemistry and mRNA in situ hybridization[J].Gynecol Oncol,1999,72(3):380-386.
  • 3[3]Massova I,Kotra LP,Fridman R,et al.Matrix metalloproteinases:structures,evolution and diversification[J].FASEB J,1999,12(12):1075-1095.
  • 4[4]Inoue Y,Abe K,Obata K,et al.Immunohistochemical studies on matrix metalloproteinase-9 (MMP-9) and type Ⅳ collage in endometrial carcinoma[J].J Obstet Gynaecol Res,1997,23(2):139-145.
  • 5[5]Davidson B,Goldberg I,Gotlieb WH,et al.Expression of matrix proteins in uterine cervical neoplasia using immunohistochemmistry[J].Eur J Obstet Gynecol Reprod biol,1998,76(1):109-114.
  • 6[6]Nuovo GJ,MacConnell PB,Simsir A,et al.Correlation of the in situ detection of polymerase chain reaction-amplified metalloproteinase complementary DNAs and their inhibitors with prognosis in cervical carcinoma[J].Cancer Res,1995,55(2):267-275.
  • 7Aznavoorian S;Murphy AN;Steller-Stevenson WG.Molecular aspects of tumor cell invasion and metastasis[J],1993(04).
  • 8Massova I;Kotra LP;Fridman R.Matrix metalloproteinases:structures,evolution,and diversification[J],1998(12).
  • 9Chambers AF;Matrisian LM.Changing views of the role of matrix metalloproteinases in metastasis[J],1997(17).
  • 10Ries C;Petrides P.Cytokine regulation of matrix metalloproteinase activity and its regulatory dysfunction in disease,1995.

共引文献56

同被引文献71

引证文献9

二级引证文献19

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部