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非小细胞肺癌组织中ZO-1的表达及其临床意义 被引量:5

Expression and Clinical Significance of ZO-1 in Patients with Non-small Cell Lung Cancer
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摘要 背景与目的已有的研究表明紧密连接蛋白-1(zonula occluden-1,ZO-1)表达和肿瘤细胞的生长和转移存在密切联系。本研究旨在探讨非小细胞肺癌(non-small cell lung cancer,NSCLC)组织中ZO-1表达的临床意义。方法应用实时荧光定量PCR、Western blot和免疫组化检测101例NSCLC癌组织及癌旁组织中ZO-1mRNA和蛋白表达,以61例肺部良性病变患者作为对照。结果 ZO-1mRNA在癌组织和肺良性病变组织间差异具有统计学意义(P<0.01)。Western blot显示:ZO-1蛋白在癌组织、癌旁组织、肺良性病变组织的相对表达量之间均存在明显差异(P<0.01或P<0.05)。免疫组化显示:ZO-1平均光密度在癌组织、癌旁组织和肺良性病变组织中分别为69.55±17.13、246.39±83.15、330.93±72.44,组间差异均具有统计学意义(P<0.01)。伴有淋巴结转移与不伴淋巴结转移肺癌组织ZO-1mRNA表达水平比较有显著性差异(t=-5.07,P<0.01),肺癌患者术后2年内生存组和2年内死亡组间ZO-1mRNA表达水平比较差异具有统计学意义(t=5.61,P<0.01)。结论 ZO-1mRNA和蛋白在NSCLC癌组织中表达降低,并与淋巴结转移的术后生存有密切关系。 Background and objective It has been proven that the expression of ZO-1 (zonula occluden-1) was correlated with the growth and metastasis of cancer. The aim of this study is to investigate the relationship between ZO-1 gene expression and clinicopathologic parameters and the survival rates in the patients with non-small cell lung cancer (NSCLC). Methods The expression levels of ZO-1 gene in 101 patients with NSCLC and lung tissues of 61 patients with benign lung disease were detected by real-time PCR, Western blot and immunohistochemical techniques. Results There was a significant statistic difference of ZO-1 mRNA expression levels between carcinoma group and control group (P〈0.01). In carcinoma group, adjacent group and control group, ZO-1 protein expression levels were with significantly statistic difference between each other (P〈0.01 or P〈0.05). There was a significantly statistic difference between ZO-1 mRNA expression levels in survival during 2 years follow-up group and death during 2 years follow-up group (t=-5.61, P〈0.01). Conclusion ZO-1 is a valuable predictive marker for NSCLC patients.
出处 《中国肺癌杂志》 CAS 2011年第2期146-150,共5页 Chinese Journal of Lung Cancer
基金 舟山市卫生局医药科研计划项目(No.2008B005)资助~~
关键词 ZO-1蛋白 肺肿瘤 免疫组织化学 ZO-1 protein Lung neoplasms Immunohistochemistry
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参考文献17

  • 1Ding GR, Qju LB, Wang XW, et al. EMP-induced alterations of tight junc- tion protein expression and disruption of the blood-brain barrier. Toxicol Lett, 2010, 196(3): 154-160.
  • 2Zhang JB, Du XG, Zhang H, et al. Breakdown of the gut barrier in patients with multiple organ dysfunction syndrome is attenuated by continuous blood purification: effects on tight junction structural proteins. Int J Artif Organs, 2010, 33(1): 5-14.
  • 3Fanning AS, Ma TY, Anderson JM. isolation and functional characteriza- tion of the actin binding region in the tight junction protein ZO-1. FASEB J, 2002, 16(13): 1835-1837.
  • 4Yu D, Marchiando AM, Weber CR, et al. MLCK-dependent exchange and actin binding region-dependent anchoring of ZO-1 regulate tight junction barrier function. Proc Natl Acad Sci USA, 2010, 107(18): 8237-8241.
  • 5Jinn Y, Inase N. Connexin 43, E-cadherin, beta-catenin and ZO-1 expression,and aberrant methylation of the connexin 43 gene in NSCLC. Anticancer Res, 2010, 30(6): 2271-2278.
  • 6Fiorini C, Gilleron J, Carette D, et al. Accelerated internalization of junctional membrane proteins (connexin 43, N-cadherin and ZO-1) within endocytic vacuoles: an early event of DDT carcinogenicity. Biochim Biophys Acta, 2008, 1778(1): 56-67.
  • 7Orban E, Szabo E, Lotz G, et al. Different expression of occludin and ZO-1 in primary and metastatic liver tumors. Pathol Oncol Res, 2008, 14(3): 299-306.
  • 8Tsukita S, Yamazaki Y, Katsuno T, et al. Tight junction-based epithelial mi- croenvironment and cell proliferation. Oncogene, 2008, 27(55): 6930-6938.
  • 9Severson EA, Kwon M, Hilgarth RS, et al. Glycogen synthase kinase 3 (GSK-3) influences epithelial barrier function by regulating Occludin, Clau- din-1 and E-cadherin expression. Biochem Biophys Res Comrnun, 2010, 397(3): 592-597.
  • 10Ko JA, Murata S, Nishida TS. Up-regulation of the tight-junction protein ZO-1 by substance P and IGF-1 in A431 ceils. Cell Biochem Funct, 2009, 27(6): 388-394.

同被引文献50

  • 1Furuse M,Hirase T,Itoh M,et al.Occludin:a novel integralmembrane protein localizing at tight junctions[J].J Cell Biol,1993,123(6):1777-88.
  • 2Fanning A S,Jameson B J,Jesaitis L A,et al.The tight junctionprotein ZO-1 establishes a link between the transmembrane proteinoccludin and the actin cytoskeleton[J].Biol Chem,1998,273(45):29745-53.
  • 3Al-Sadi R M,Ma T Y.IL-1 beta causes an increase in intestinalepithelial tight junction permeability[J].J Immunol,2007,178(7):4641-9.
  • 4Kaihara T,Kawamata H,Imura J,et al.Rediffereniation and ZO-1reexpression in liver-metastasized colorectal cancer:possible associ-ation with epidermal growth factor receptor-induced tyrosine phos-phorylation of ZO-1[J].Cancer Sci,2003,94(2):166-72.
  • 5Youakim A,Ahdieh M.Interferon-gamma decreases barrier func-tion in T84 cells by reducing ZO-1 levels and disrupting apical ac-tin[J].Am J Physiol,1999,276(5):1279-88.
  • 6Tobioka H,Isomura H,Kokai Y,et al.Occludin expression de-creases with the progression of human endometrial carcinoma[J].Hum Pathol,2004,35(2):159-64.
  • 7Tobioka H,Tokunaga Y,Isomura H,et al.Expression of occludin,atight-junction-associated protein,in human lung carcinomas[J].Virchows Arch,2004,445(5):472-6.
  • 8Tokunaga Y,Tobioka H,Isomura H,et al.Expression of occlu-din in human rectal carcinoid tumours as a possible marker forglandular differentiation[J].Histopathology,2004,44(3):247-50.
  • 9Busch C,Hanssen T A,Wagener C,et al.Down-regulation ofCEACAM1 in human prostate cancer:correlation with loss of cellpolarity,increased proliferation rate,and Gleason grade 3 to 4 tran-sition[J].Hum Pathol,2002,33(3):290-8.
  • 10Osanai M,Murata M,Nishikiori N,et al.Occludin-mediated pre-mature senescence is a fail-safe mechanism against tumorigenesisin breast carcinoma cells[J].Cancer Sci,2007,98(7):1027-34.

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