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Connexin 43和E-cadherin在非小细胞肺癌中表达及相关性研究 被引量:4

Expressions of connexin 43 and E-cadherin and their correlation in non-small cell lung cancer
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摘要 背景与目的 由连接蛋白(connexin,Cx)构成的细胞间隙连接(gap junction)对细胞的增殖和分化起着重要的调控作用,Cx表达下降将导致细胞恶化。上皮钙粘蛋白(E cadherin)为上皮细胞与细胞之间及细胞与细胞外基质粘附的跨膜糖蛋白分子,其功能抑制或表达下降可使细胞间粘附能力下降,细胞易于分离。本研究旨在探讨连接蛋白43(Connexin 43,Cx43)和E cadherin在非小细胞肺癌中的表达及两者的相互关系。方法 采用免疫组织化学S P法检测85例原发性非小细胞肺癌组织的Cx43和E cadherin蛋白表达,并进行两者的相关性分析。结果 Cx43和E cadherin蛋白在非小细胞肺癌中表达显著下降,其下降程度与肺癌的细胞分化程度、pTNM分期和有无淋巴结转移均有密切关系,而与组织学分型无明显关系。Cx43 和E cad herin蛋白表达之间存在明显的相关性。结论 Cx43和E cadherin蛋白在非小细胞肺癌中表达显著下降,且两者存在着明显的相关性,可能是肺癌发生和发展过程中的共同事件。 Background and objective Connexin (Cx), a transmembranous protein, makes up of gap junction, which induces the communication of cells and plays an important role in proliferation and differentiation of cells. The directly or indirectly reduced expression of connexin protein may induce a malignant tendency of cells. E-cadherin is a transmembranous glycoprotein and induces the adhesion of epitheliums and extracellular matrix. The reduced expression or dysfunction of E-cadherin will impair the ability of adhesion and make cells easy to be isolated. The aim of this study is to examine the expressions of Connexin 43 (Cx43) and E-cadherin in non-small cell lung cancer (NSCLC), and to analyze their correlation. Methods The expressions of Cx43 and E-cadherin proteins were detected in 85 primary NSCLC samples by immunohistochemistry S-P method, and their correlation was then analyzed. Results The expressions of Cx43 and E-cadherin were remarkably decreased in NSCLC tissues. Cx43 and E-cadherin expressions were related to cell differentiation, pTNM stage and lymphatic metastasis of NSCLC. The expression of Cx43 significantly correlated with the expression of E-cadherin. Conclusion The expressions of Cx43 and E-cadherin significantly decrease in NSCLC and they correlate with each other. It might be common affairs in carcinogenesis and development of NSCLC.
出处 《中国肺癌杂志》 CAS 2005年第2期103-106,共4页 Chinese Journal of Lung Cancer
基金 国家自然科学基金(No.30470764)资助~~
关键词 非小细胞肺癌 CONNEXIN 43 E—cadherin 免疫组织化学 Non-small cell lung cancer Connexin 43 E-cadherin Immunohistochemistry
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  • 1邱雪杉,杨秀,李庆昌,王恩华.上皮性钙黏附蛋白和β-连环素的表达与非小细胞肺癌预后的关系[J].中华病理学杂志,2002,31(4):318-321. 被引量:24
  • 2范松青,周鸣,向秋,王洁如,熊伟,王蓉,魏启幼,周金平,李桂源.细胞间隙连接蛋白在多种类型癌组织中的原位表达研究[J].癌症,2003,22(7):686-690. 被引量:16
  • 3Nemeth L, Rolle U, Puri P. Altered cytoskeleton in smooth muscle of aganglionic bowel. Arch Pathol Lab Med,2002,126(6):692-696.
  • 4杨秀,李庆昌,邱雪杉,王恩华.非小细胞肺癌中E-cadherin表达及与临床病理因素的关系[J].中国医科大学学报,2000,29(5):323-324. 被引量:2
  • 5Chen JT, Cheng YW, Chou MC, et al. The correlation between aberrant connexin 43 mRNA expression induced by promoter methylation and nodal micrometastasis in non-small cell lung can-cer. Clin Cancer Res,2003,9(11):4200-4204.
  • 6Chen Y, Huhn D, Knosel T, et al. Downregulation of connexin 26 in human lung cancer is related to promoter methylation. Int J Cancer,2005,113(1):14-21.
  • 7Zhang YW, Kaneda M, Morita I. The gap junction-independent tumor-suppressing effect of connexin 43. J Biol Chem,2003,278(45):44852-44856.
  • 8Ko K, Arora P, Lee W, et al. Biochemical and functional characterization of intercellular adhesion and gap junctions in fibroblasts. Am J Physiol Cell Physiol,2000,279(1):C147-C157.
  • 9Hernandez-Blazquez FJ, Joazeiro PP, Omori Y, et al. Control of intracellular movement of connexins by E-cadherin in murine skin papilloma cells. Exp Cell Res,2001,270(2):235-247.
  • 10Yano T, Yamasaki H. Regulation of cellular invasion and matrix metalloproteinase activity in HepG2 cell by connexin 26 transfection. Mol Carcinog,2001,31(2):101-109.

二级参考文献9

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同被引文献27

  • 1安君岭,徐正顺,张天一,张朝晖.肝细胞癌中间隙连接蛋白Cx43和E-钙粘附素的表达[J].实用肿瘤学杂志,2005,19(4):257-260. 被引量:5
  • 2TSAI H, WERBER L, DAVIA M O, et al. Reduced connexin 43 expression in high grade, human prostatic adenocarcinoma cells[J]. Biochem Biophys Res Commum , 1996,227:64-67.
  • 3HIROHASHI S. Inactivation of the E-cadherin-mediated cell adhesion system in human cancers[J]. Am J Pathol, 1998, 153 : 333-335.
  • 4OYAMADA M, KIMURA H, OYAMADA Y, et al. The expression, phosphorylation, and localization of connexin 43 and gap junctional intercellular communication during the establishment of a synchronized contraction of cultured neonatal rat cardiac myocytes[J]. Ezp Cell Res, 1994,212:351.
  • 5HIRSCHI K K, XU C E, TSUKAMOTO T, et al. Gap junc tion genes Cx26 and Cx43 individually suppress the cancer phenotype of human mammary caicinoma cells and restore differentiation potential[J]. Cell Growth Differ, 1996,7:861.
  • 6HERNAND E Z, BLAZQUEZ F J, JOAZEIRO P P, et al. Control of intracellular movement of connexins by E-eadherin in murine skin papilloma cells[J]. Exp Cell Res, 2001,270 : 235.
  • 7YANO T, YAMASAKI H. Regulation of cellular invasion and matrix metalloproteinase activity in Hep G2 cell by connexin 26 transfection[J]. Mol Carcinog, 2001,31 : 101-109.
  • 8Abbaci M, Barberi - Heyob M, Stines JR, et al. Gap junctional intercellular communication capacity by gap-FRAP technique: a comparative study[ J]. Biotechnol J ,2007,2( 1 ) :50-61.
  • 9Baumgart E, Cohen MS, Nero BS, et al. Identification and prognostic significance of an epithelial - mesenchymal transition expression profile in human bladder tumors[J]. Clin Cancer Res, 2007, 13 (6) : 1685- 1694.
  • 10Gao FH,Wang Q, Wu YL,et al. c- Jun N- terminal kinase mediates AML1 - ETO protein - induced connexin- 43 expression[J]. Biochem Biophys Res Commun,2007,356(2) :505-511.

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