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E-cadherin、β-catenin、FAK在大肠癌的表达及其意义 被引量:11

Expression of E-cadherin,β-catenin and FAK in Colorectal Carcinoma and Their Signi-ficances
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摘要 目的探讨β连环素(βcat)、上皮钙黏附素(Ecad)和黏着斑激酶(FAK)在大肠癌发生、发展中的作用。方法采用免疫组织化学方法检测了12例正常大肠黏膜,28例大肠腺瘤及49例大肠癌组织的βcat、Ecad和FAK表达情况。结果大肠癌βcat异位表达率61.2%,显著高于大肠腺瘤(35.7%P<0.05)。大肠癌βcat、Ecad膜表达缺失率分别为67.3%,57.1%,显著高于正常大肠黏膜和大肠腺瘤(P<0.01,P<0.01)。大肠癌FAK阳性率65.3%,高于大肠腺瘤和正常大肠黏膜(P<0.01)。βcat异位表达、βcat和Ecad膜表达缺失、FAK表达与大肠癌的浸润程度、淋巴结转移和Dukes分期等因素有关。大肠癌中,FAK表达与βcat、Ecad膜表达缺失及βcat异位表达呈正相关。结论βcat异位表达可能参与了大肠癌的发生、发展。βcat和Ecad膜表达缺失、βcat异位表达、FAK表达可能与大肠癌的侵袭和转移有关,此过程中,FAK可能抑制了癌细胞之间的黏附。 Objective To investing ate the role of β-catenin, Kcadherin and FAK in the carcinogenesis and progression of colorectal carcinoma. Methods Expression of β-catenin, E-cadherin and FAK was exam- ined immunohistochemically in 12 cases of normal colorectal mucosa,28 cases of colorectal adenoma,49 cases of colorectal carcinoma. Results The rate of cytoplasmic and/or nuclear expression of β-catenin was 61.2% in coloretal carcinoma,which was significantly higher than that in colorectal adenoma(35. 7%, P (0. 05). The rate of the reduced membranous expression of β-catenin and E-cadherin was 67. 30/00, 57. 1% respectively in colorectal carcinoma, which was significantly higher than that in the colorectal adenoma and normal colorectal epithelium. The rate of FAK expression was 65. 3% in colorectal carcinoma, which was significantly higher than that in the colorectal adenoma and in the normal colorectal epithelium (P〈0. 01 ). In addition, the last four kinds of expression was associated with degree of soakage, lymph node metastasis and Dukes stage. There was a positive correlation between FAK expression and the re duced membranous expression of β-catenin might play a role in the carcinogenesis and progression of colorectal carcinoma. Conclusion The cytoplasmic and/or nuclear expression of β-catenin, the reduced membranous expression of β-catenin and E-cadherin and FAK expression might be related to the invasion and metastasis of colorectal carcinoma, In which FAK might restrain the adhesion among carcinoma cells.
出处 《肿瘤防治研究》 CAS CSCD 北大核心 2005年第9期542-544,共3页 Cancer Research on Prevention and Treatment
关键词 Β-连环素 上皮钙黏附素 黏着斑激酶 大肠癌 β-cat E-cad FAK Colorectal Carcinoma
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参考文献9

  • 1Maruyama K, Ochiai A, Akimoto S, et al. Cytoplasmic betacatenin accmnulation as a predictor of hematogenous metastasis in human colorectal cancer[J]. Oncology, 2000,59 (4) : 302-309.
  • 2NigamAK, SavageFJ, Boulos PB, et al. Loss of cell-cell and cellmatrix adhesion molecules in colorectal cancer[J]. Br Cancer,1993,68(3) :507-514.
  • 3Gunther K,Brabletz T,Kraus C, et al. Predictive value of nuclear beta - catenin expression for the occurrence of distant metastases in rectal cancer [J ]. Dis Colon Rectum, 1998, 41(10): 1256-1261.
  • 4Dorudi S, Hanby AM,Poulsom R,et al. Level of expression of E-cadherin mRNA in colorectal cancer correlates with clinical outcome[J]. Br J cancer, 1995,71 (3) :614-616.
  • 5向德兵,吴晓华,李增鹏,刘友生.大肠癌β-连环素和上皮钙黏附素表达及其意义[J].肿瘤防治杂志,2002,9(1):39-42. 被引量:8
  • 6倪俊,陈玉林.粘着斑激酶[J].生理科学进展,1999,30(4):367-372. 被引量:4
  • 7Withers BE, Hanks SK, Fry DW. Correlations between the expression phosphotyosine content and enzymatic activity of focal adhesion kinase, PP125FAK, in tumor and nontransformed cell[J]. Cancer Biochem Biophys, 1996,15(3): 127-139.
  • 8Ayaki M, Komastu K, Mukai M, et al. Reduced expression of FAK in liver metastases compared with matched primary human colorectal adenocarcinoma [J ]. Clin Cancer Res, 2001,7(100) :3106-3112.
  • 9Avizienyte E,Wyke AW. Scr-induced deregulation of E-cadherin in colon cancer cdlls requires integrin signaling[J]. Nat Cell Biol, 2002,4 (8) : 632-638.

二级参考文献11

  • 1Zheng C,J Biol Chem,1998年,273卷,2384页
  • 2Park BH,Vogelstein B,Kinzler KW.Genetic disruption of PPARdelta decreases the tumorigenicity of human colon cancer cells[].Proceedings of the National Academy of Sciences of the United States of America.2001
  • 3Jawhari AU,Farthing MJ,Pignatelli M.The E-cadherin epidermal growth factor receptor interaction: a hypothesis of reciprocal and reversible control of intercellular adhesion and cell proliferation[].Journal of Paleopathology.1999
  • 4Rashid A,Gao YT,Bhakta S,et al.Beta-catenin mutations in biliary tract cancers: a population-based study in China[].Cancer Research.2001
  • 5Shun CT,Wu MS,Lin MT,et al.Immunohistochemical evaluation of cadherin and catenin expression in earlygastric carcinomas: correlation with clinicopathologic characterstics and Helicobacter pylori infection[].Oncology.2001
  • 6Wong CM,Fan ST,Ng IO.beta-Catenin mutation and overexpression in hepatocellular carcinoma: clinicopathologic and prognostic significance[].Cancer.2001
  • 7Hugh TJ,Dillon SA,Taylor BA,et al.Cadherin-catenin expression in primary colorectal cancer: a survial analysis[].British Journal of Cancer.1999
  • 8Shih IM,Yu J,He TC,et al.The β-catenin binding domain of adenomatous polyposis coli is sufficient for tumor suppression[].Cancer Research.2000
  • 9Brabletz,T,Herrmann K,Jung A,et al.Expression of nuclear betacatenin and cmyc is correlated with tumor size but not with proliferative activity of colorectal adenomas[].American Journal of Pathology.2000
  • 10Saegusa M,Okayasu I.Frequent nuclear beta-catenin accumulation and associated mutations in endometrioid-type endometrial and ovarian carcinomas with squamous differentiation[].Journal of Paleopathology.2001

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