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β-catenin和COX-2在大肠癌中的表达及临床意义 被引量:5

Expression and Clinical Significance of β-catenin and COX-2 in Human Colorectal Carcinoma
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摘要 目的探讨β-catenin和COX-2在大肠癌中的表达及临床意义。方法采用免疫组化技术检测153例大肠组织标本中β-catenin和COX-2的表达水平,并对其临床意义和相互关系进行统计学分析。结果β-catenin在细胞膜上的丢失与腺癌的分化程度、Dukes分期及淋巴结转移具有相关性(P<0.05);COX-2的过表达与腺癌的Dukes分期、淋巴结转移和浸润程度具有相关性(P<0.05);β-catenin的异位表达与COX-2的过表达没有相关性。结论细胞膜上β-catenin的表达减少在分化程度低、Dukes分期晚及有淋巴结转移的患者中更明显。COX-2的表达水平在Dukes分期晚、浸润程度及有淋巴结转移的患者中增高更明显。腺癌中β-catenin的异位表达可能不是COX-2过表达的主要原因。β-catenin和COX-2可能是Dukes分期和判断淋巴结转移风险的一个较好的指标。 Objective To investigate the expression and clinical significance of β-catenin and COX-2 in human colorectal carcinoma. Methods [WTBZ]The expression of β-catenin and COX-2 in 153 colorectal tissue specimens was examined by immunohistochemical technique, and their clinical significance and correlation were statistically analyzed. Results In colorectal adenocarcinoma, the loss of β-catenin in the cytomembrane was significantly correlated with the differentiated degree, lymph node metastasis and Dukes' stages, while COX-2 overexpression was associated with the Dukes' stages,lymph node metastasis and infiltrating depth. The ectopic expression of β-catenin was not associated with the COX-2 overexpression. [WTHZ] Conclusion COX-2 and β-catenin may play a role in the pathogenesis of colorectal adenocarcinoma. The ectopic expression of β-catenin may be not the main reason of the COX-2 overexpression in colorectal adenocarcinoma. Detection of β-catenin and COX-2 expression may be helpful for Dukes' staging and evaluating the risk of lymph node metastasis in colorectal adenocarcinoma.
出处 《中国医师杂志》 CAS 2005年第7期889-891,共3页 Journal of Chinese Physician
关键词 Β-CATENIN COX-2 大肠癌 表达 免疫组化 Colorectal neoplasms/pathology β-catenin Cyclooxygenase-2 Wnt signal pathway Immunohistochemistry
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  • 1来茂德.β-catenin and related factors in colorectal tumorigenesis [J].Chinese Journal of Clinical and Experimental Pathology (临床与实验病理学杂志),2000,16(5):412-414. 被引量:1
  • 2黄智达 来茂德.Molecular mechanisms of colorectal adenomagenesis [J].Chinese Journal of Clinical and Experimental Pathology (临床与实验病理学杂志),1999,15(3):235-237. 被引量:1
  • 3[4]Harris RE, Kasbari S, Farrar WB. Prospective study of nonsteroidal anti-inflammatory drugs and breast cancer [ J]. Oncol Rep, 1999, 6(1):71-73. 被引量:1
  • 4[5]Harris RE, Alshafie GA, Abou Issa H, et al. Chemoprevention of breast cancer in rats by celecoxib, a cyclooxygenase-2 inhibitor [J].Cancer Res, 2000, 60(8) :2101-2103. 被引量:1
  • 5[6]Ristimaki A, Sivula A, Lundin J, et al. Prognostic significance of elevated cyclooxygenase-2 expression in breast cancer [J].Cancer Res, 2002, 62(3):632-635. 被引量:1
  • 6[7]DiGiovanna MP, Chu P, Davison TL, et al. Active signaling by HER-2/neu in a subpopulation of HER-2/neu-overexpressing ductal carcinoma in situ: clinicopathological correlates [J].Cancer Res, 2002, 62(22) :6667-6673. 被引量:1
  • 7[8]Subbaramaiah K, Norton L, Gerald W, et al. Cyclooxygenase-2 is overexpressed in her-2/neu-positive breast cancer. Evidence for involvement of AP-1 and PEA3 [J]. J Biol Chem, 2002, 277(21): 18649- 18657. 被引量:1
  • 8[1]Parrett ML, Harris RE, Joarder FS, et al. Cyclooxygenase-2 expression in human breast cancer [J]. Int J Oncol, 1997,10(6):503-507. 被引量:1
  • 9[2]Eli Y, Przedecki F, Levin G, et al. Comparative effects of indomethacin on cell proliferation and cell cycle progression in tumor cells grown in vitro and in vivo [J]. Biochem Pharmacol, 2001,61(5):565-571. 被引量:1
  • 10[3]Soslow RA, Dannenberg AJ, Rush D, et al. COX-2 is expressed in human pulmonary, colonic, and mammary tumors [J]. Cancer, 2000, 89(12):2637- 2645. 被引量:1

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