期刊文献+

高迁移率族蛋白B1和基质金属蛋白酶-9在宫颈鳞癌中的表达及其临床意义 被引量:11

Expressions of High Mobibity Group Box 1 Protein and Matrix Metalloproteinase-9 in Cervical Squamous Epithelial Carcinoma and Their Clinical Significance
原文传递
导出
摘要 目的:研究宫颈鳞癌中高迁移率族蛋白B1(HMGB1)和基质金属蛋白酶-9(MMP-9)表达情况,及其与宫颈癌临床病理特征的关系。方法:应用免疫组化法检测宫颈鳞癌及正常宫颈组织中HMGB1和MMP-9的表达情况。结果:HMGB1在对照组、原位癌和宫颈浸润癌中的阳性率分别为15.8%(3/19)、53.3%(8/15)和80.0%(32/40),P<0.01;HMGB1的表达与宫颈癌临床分期有关(P<0.05),与患者的年龄、病理分级、淋巴结转移无关(P>0.05)。MMP-9在对照组、原位癌和浸润癌中的阳性率分别为21.5%(4/19)、53.3%(8/15)和65.0%(26/40),P<0.01。宫颈癌中HMGB1与MMP-9的共同阳性表达率为47.3%(26/55),rs=0.305,P<0.05。结论:HMGB1与宫颈癌的发生有关,HMGB1与MMP-9表达呈正相关,提示HMGB1可能与宫颈癌的浸润、转移有关。 Objective: To investigate the expressions of High Mobility Group Box 1(HMGB1) and matrix metalloproteinase-9(MMP-9) in human cervical squamous epithelial carcinoma(CSEC),and to explore the relationship among HMGB1,MMP-9 and clinical pathological characteristics of CSEC.Methods: Immunohistochemisty methods were adopted to detect the expressions of HMGB1 and MMP-9 in cervical squamous epithelial infiltrating carcinoma(CSEIC),carcinoma in situ(CIS) and normal control groups.Results: The positive expression rate of HMGB1 in CSEIC,CIS and control group was 80.0%(32/40),53.3%(8/15) and 15.8%(3/19),respectively,with a significant difference among them(P〈0.01).The expression of HMGB1 had no relation with age,differentiation degree,lymphatic metastasis or clinical classification(all P〉0.05).The positive expression rate of MMP-9 in CSEIC,CIS and control group was 65.0%(26/40),53.3%(8/15) and 21.5%(4/19),respectively(P〈0.01).There is a positive correlation between the expression of HMGB1 and MMP-9 in CSEC,and their co-positive rate was 47.3%(26/55,rs=0.305,P〈0.05).Conclusion: HMGB1 plays a role in the development of CSEC.The expressions of HMGB1 and MMP-9 in CSEC have a positive correlation with each other,which suggests that HMGB1 might be related with the invasive and metastasis of cervical carcinoma.
出处 《武汉大学学报(医学版)》 CAS 北大核心 2010年第3期343-346,共4页 Medical Journal of Wuhan University
基金 湖北省卫生厅重点项目(编号:JX3A17) 湖北省自然科学基金资助项目(编号:2007ABA056)
关键词 高迁移率族蛋白1 基质金属蛋白酶-9 宫颈癌 宫颈原位癌 免疫组化 High Mobility Group Box 1 Matrix Metalloproteinase-9 Cervical Neoplasms Carcinoma in Situ Immunohistochemisty
  • 相关文献

参考文献9

  • 1Ellerman JE, Brown CK, Zeh H J, et al. Masquerader: high mobility group Box-1 and cancer[J]. Clinical Cancer Research, 2007,13(10) :2 836-2 848.
  • 2Sheu BC, Lien HC, Ho HN, et al. Increased expression and activation of gelatinolytic matrix metalloproteinases is associated with the progression and recurrence of human cervical cancer[J].Cancer Res, 2003, 63 (19) :6 537-6 542.
  • 3Bandiera A, Bonifacio D, Manfioletti G, et al. Expression of HMGI(Y) proteins in squamous intraepithelial and invasive lesions of the uterine cervix[J]. Cancer Res, 1998,58(3):426-431.
  • 4付欣,杜晓琴,郝权.宫颈鳞癌组织高迁移率族蛋白HMGB1表达及其临床意义的研究[J].中华肿瘤防治杂志,2008,15(5):357-359. 被引量:22
  • 5Evans A, Lennard TW, Davies BR. High-mobility group protein 1 (Y) : metastasis-associated or metastasis-inducing[J]. J Surg Oncol, 2004, 88(2) :86-99.
  • 6Mitola S, P, elleri M, Urbinati C, et al. Cutting edge: extracellular high mobility group box-1 protein is a proangiogenic cytokine[J].J Immunol, 2006, 176(1):12-15.
  • 7Reeves R, Edberg DD, Li Y. Architectural transcription factor HMGI(Y) promotes tumor progression and mesenchymal transition of human epithelial cells[J]. Mol Cell Biol, 2001, 21(2):575-594.
  • 8Taguchi A, Blood DC, del Toro G, et al. Blockade of RAGE-amphoterin signalling suppresses tumour growth and metastases[J].Nature, 2000, 405(6 784):354-360.
  • 9黄庆先,王国斌,孙念峰,王春友.高迁移率族蛋白框1反义核酸抑制人胰腺癌细胞系PCNA-1侵袭的研究[J].癌症,2004,23(9):1036-1040. 被引量:16

二级参考文献18

  • 1郭社珂,乔玉环,赵先兰.宫颈癌广泛子宫全切及盆腔淋巴结清除术后血清蛋白质变化[J].中华肿瘤防治杂志,2006,13(22):1730-1733. 被引量:3
  • 2Taguchi A, Blood DC, del Toro G, et al. Blockage of RAGE amphoterin signalling suppresses tumour growth and metastasis [J]. Nature, 2000, 405(6784): 354- 360.
  • 3Rauvala H, Huttunen HJ, Fages C, et al. Heparin binding proteins HB GAM (pleiotrophin) and amphoterin in the regulation of cell mobility [J]. Matrix Biol, 2000, 19(5): 377- 387.
  • 4J萨姆布鲁克 E F 弗里奇 T 曼尼阿蒂斯 16-392.分子克隆实验指南 [M](第 2版)[M].北京:科学出版社,1999..
  • 5Zi X, Grasso AW, Kung HJ, et al. A flavonoid antioxidant, silymarin, inhibits activation of erbB1 signaling and induces cyclin dependent kinase inhibitors, G1 arrest, and anticarcinogenic effects in human prostate carcinoma DU145 cells[J]. Cancer Res, 1998, 58(9): 1920 1929.
  • 6Heussen C, Dowdle EB. Electrophoretic analysis of plasminogen activation in polyacrylamide gels containing sodium dodecyl sulfate and copolymerized substrates [J]. Anal Biochem, 1980, 102(1): 196- 202.
  • 7Albini A, Iwamoto Y, Kleinman HK, et al. A rapid in vitro assay for quantitating the invasion potential of tumor cells [J]. Cancer Res, 1987, 47(12): 3239- 3245.
  • 8Thomas JO, Travers AA. HMG1 and 2, and related architectural DNA binding proteins [J]. Trends Biochem Sci, 2001, 26(3): 167- 174.
  • 9Kuniyasu H, Chihara Y, Kondo H, et al. Differential effects between amphoterin and advanced glycation end products on colon cancer cell [J]. Int J Cancer, 2003, 104(6): 722- 727.
  • 10Sternlicht MD, Werb Z. How matrix metalloproteinases regulate cell behavior [J]. Annu Rev Cell Dev Biol, 2001, 17: 463- 516.

共引文献35

同被引文献96

引证文献11

二级引证文献23

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