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Srx与E-cadherin在宫颈鳞癌组织中的表达及临床意义 被引量:7

The expression and clinical significance of Srx and E-cadherin in cervical squamous cell carcinoma tissue
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摘要 目的探讨硫氧还原蛋白(Sulfiredoxin,Srx)与上皮细胞黏附分子E-钙黏蛋白(E-cadherin)在宫颈鳞癌组织中的表达及临床意义。方法采用免疫组织化学SABC法检测30例正常宫颈上皮组织(NC)、20例重度子宫颈上皮内瘤变(HSIL)及104例宫颈鳞状细胞癌(CSCC)组织中Srx和E-cadherin蛋白的表达情况,分析两者与宫颈鳞癌临床病理特征的关系及两者表达的相关性。结果 Srx在宫颈鳞癌组织中呈现高表达,而E-cadherin在鳞癌组织中表达明显降低,2蛋白阳性表达率在3组中比较差异具有统计学意义(P<0.05),且Srx与E-cadherin蛋白表达呈负相关。宫颈鳞癌组织中Srx的表达与淋巴结转移、肿瘤浸润深度及有无脉管浸润有关(P<0.05),而与患者年龄、临床分期、肿瘤大小及癌组织分化程度无关(P>0.05)。E-cadherin的阳性表达率与肿瘤大小、组织分化程度及淋巴结转移关系密切(P<0.05)。结论宫颈鳞癌组织中Srx的高表达与恶性临床病理特征密切相关,并与Ecadherin蛋白表达呈负相关,提示Srx可能通过调控EMT促进宫颈鳞癌进展。 This study designed to investigate the expression and clinical significance of Sulfiredoxin(Srx) and E-cadherin in cervical squamous cell carcinoma tissues. Immunohistochemical SABC method was used to detect the expression levels of Srx and E-cadherin in specimens from 30 cases from normal cervical squamous cell epithelium(NC), 20 cases of high-grade squamous intraepithelial lesions(HSIL) and 104 cases of cervical squamous cell carcinoma(CSCC). The correlation between Srx expression and E-cadherin expression and the correlation between the two proteins and clinicopathological characteristics of cervical squamous cell carcinoma were analyzed. Data showed that the expression of Srx was up regulated but E-cadherin was obviously decreased in CSCC tissues; the differences of the positive expression rate of Srx and E-cadherin in three groups were statistically significant(P〈0.05); Srx and E-cadherin expression were negatively correlated in CSCC tissues. Srx was signifiantly correlated with cervical squamous cell carcinoma of lymph node metastasis, cancer invasion depth and haemal tube infiltration(P〈0.05), but Srx expression did not correlate with age, clinical stage(FIGO), volume of primarily tumor and degree of differentiation(P〈0.05). E-cadherin was closely correlated with cervical squamous cell carcinoma of primarily tumor volume, differentiation degree and lymph node metastasis(P〈0.05). In conclusion, the overexpression of Srx in cervical squamous cell carcinoma is correlated with malignant clinicopathological characteristics, and negatively correlated with E-cadherin expression, which indicates that Srx may promote the development of cervical squamous cell carcinoma by regulating EMT.
出处 《免疫学杂志》 CAS CSCD 北大核心 2015年第12期1067-1071,共5页 Immunological Journal
关键词 硫氧还原蛋白 E-钙黏蛋白 宫颈鳞癌 免疫组组化学 Sulfiredoxin E-cadherin Cervical squamous cell carcinoma Immunohistochemistry
作者简介 通信作者:王辉.E—mail:15310918845@163.com
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参考文献20

  • 1Biteau B, Labarre J, Toledano MB. ATP-dependent reduction of cysteine-sulphinic acid by S. cerevisiae sulphiredoxin [J]. Nature, 2003, 425(6961): 980-984.
  • 2Hartikainen JM, Tengstrom M, Kosma VM, et al. Genetic polymorphisms and protein expression of NRF2 and Sulfiredoxin predict survival outcomes in breast cancer [J]. Cancer Res, 2012, 72(21): 5537-5546.
  • 3Wei Q, Jiang H, Xiao Z, et al. Sulfiredoxin-Peroxiredoxin IV axis promotes human lung cancer progression through modulation of specific phosphokinase signaling[J]. Proe Natl Acad Sei USA, 2011, 108(17): 7004-7009.
  • 4Gao Q, Liu W, Cai J, et al. EphB2 promotes cervical cancer progression by inducing epithelial--mesenchymal transition [J]. Hum Pathol, 2014, 45(2): 372-381.
  • 5Wang WS, Yu SL, Yang XS, et al. Expression and significance of twist and E-cadherin in ovarian cancer tissues[J]. Asian Pac J Cancer Pre, 2013, 14(2): 669-672.
  • 6Fulga V, Rudico L, Balica AR, et al. Differential expression of e-cadherin in primary breast cancer and corresponding lymph node metastases[J]. Anticancer Res, 2015, 35(2): 759-765.
  • 7Ha B, Kim EK, Kim JH, et al. Human peroxiredoxin 1 modulates TGF-betal-induced epithelial-mesenchymal transition through its peroxidase activity[J]. Biochem Biophys Res Commun, 2012, 421(1): 33-37.
  • 8王凤杰,王科坤,陈显兵,向海付,桑才艺,刘锦红,刘昕.宫颈癌组织中DCR3表达与外周血T细胞亚群的相关性研究[J].免疫学杂志,2015,31(3):246-249. 被引量:8
  • 9Kwak MK, Wakabayashi N, Itoh K, et al. Modulation of gene expression by cancer chemopreventive dithiolethionesthrough the Keapl-Nrf2 pathway. Identification of novel gene clusters for cell survival[J]. J Biol Chem, 2003, 278(10): 8135-8145.
  • 10Wei Q, Jiang H, Baker A, et al. Loss of sulfiredoxin renders mice resistant to azoxymethane/dextran sulfate sodium- induced colon carcinogenesis[J]. Carcinogenesis, 2013, 34(6): 1403-1410.

二级参考文献47

  • 1刘瑞振,张长弓,何琼,苏金华,陈彩霞,陈福,庄国洪.抗人DcR3单克隆抗体的制备、鉴定及应用[J].免疫学杂志,2009(1):34-38. 被引量:8
  • 2何春年,刘贵香,翟金萍,徐翠清,赵焕芬,孙金海.子宫颈鳞癌组织中T、B、NK淋巴细胞浸润与肿瘤免疫[J].免疫学杂志,2005,21(B06):115-118. 被引量:4
  • 3陈莉,李德春,朱远源.NET-1蛋白表达与肝癌临床病理因素相关性探讨[J].中华病理学杂志,2005,34(9):596-597. 被引量:23
  • 4Yang CR, Hsieh SL, Ho FM, et al. Decoy receptor 3 increases monocyte adhesion to endothelial cells via NF- Kappa B dependent up-regulation of intercellular adhesion molecule-l, VCAM-1 and IL-8 expression[J]. J Immunol, 2005, 174(3): 1647-1656.
  • 5Chang YC, Chan YH, Janckson DG, et al. The glycosamuoglycan-binding domain of decoy receptor is essential for induction monocyte adhesion[J]. J Immunol, 2006, 176(1): 173-180.
  • 6Gill RM, Coleman NM, Hunt JS. Differential cellular expression of LIGHT and its receptors in early gestation human placentas[J]. J Reprod Immunol, 2007, 74(1/2): 1-6.
  • 7Connolly K,Cho YH, Duan R, et al. In vivo inhibition of Fas ligand-mediated killing by TR6, a Fas ligand decoy receptor[J]. J Pharmacol Exp Ther, 2001, 298(1): 25-33.
  • 8Nedergaard BS, Ladekarl M, Thomsen HF. Iw density of CD3, CD4 and CD8 cells is associated with increased risk of relapse in squamous cell cervical cancer[J]. Br J Cancer, 2007, 97(8): 1135-1138.
  • 9Passmore JA,Milner M,Denny L. Comparison of cervical and blood T cell responses to human papillomavirus 16 in women with human papillomavirus associated cervical intraepithelial neoplasia[J]. Immunology, 2006, 119(4): 507- 514.
  • 10Gill RM, Huntr JS. Soluble receptor (DCR3) and cellular inhibitor of apoptosis - 2 (cIAP - 2 ) protect human cytotrophoblast cells against LIGHT-mediated apoptosis[J]. Am J Pathol, 2004, 165(1): 309-317.

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