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程序性细胞死亡因子4在胃癌组织中的表达及临床病理学意义 被引量:16

Expression of programmed cell death factor 4 and its pathological significance in gastric cancer
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摘要 目的:探讨胃癌组织中程序性细胞死亡因子4(programmed cell death 4,PDCD4)的表达及其临床病理学意义。方法:应用免疫组织化学和Western印迹杂交研究方法检测61例胃癌组织中PDCD4的表达,观察其与胃癌临床病理学参数之间的关系。结果:免疫组化染色显示,在正常胃组织中,阳性细胞比例均在80%以上。61例胃癌中,PDCD4低表达者(阳性细胞比例〈30%)占65.6%(40/61),高表达(阳性细胞比例介于30%~80%)者占34.4%(21/61)。Western印迹分析结果显示,同癌旁正常组织相比,所有胃癌组织PDCD4蛋白表达均明显下调。相关分析表明,PDCD4表达下调或缺失与肿瘤的不良分化相关,P〈0.01,而与性别、年龄厦肿瘤的TNM分期无关。结论:PDCD4蛋白在胃癌中多呈低表达,并与胃癌的分化程度有关,在胃癌的发生、发展过程中起重要作用。 OBJECTIVE: To investigate the expression of programmed cell death factor 4 (PDCD4) protein and its clinicopathological significance in gastric cancer. METHODS:PDCD4 expression in 5 fresh specimens of gastric cancer and relevant adjuvant non-cancerous tissue were detected by Western blot with PDCD4 specific antibody; immunohistochemistry was used to examine the expression of PDCD4 in 61 paraffin embedded specimens of gastric cancer, among which 26 specimens had adjacent normal gastric tissue. Correlations of PDCD4 expression with clinico-pathological data were analyzed. RESULTS: The expression of PDCD4 was significantly lower in all 5 fresh gastric cancer tissues than in non-cancerous tissues detected by Western blot. Compared with adjuvant normal gastric tissue (〉80% of positive cells), low PDCD4 expression was shown in 61 gastric cancer tissues (〈30% of positive cells in 40 cases and 30%-80% of positive cells in 21 cases). In the 21 cases that positive cells was between 30% and 80%, the rates of well, moderately, and poorly differentiated patients were 57.1%, 33.3% and 9.6%, respectively. However, in the 40 cases that positive cells was less than 30%, the rates of well, moderately, and poorly differentiated patients were 2.5%, 37.5% and 60%, respectively. In moderately and poorly differentiated patients, 68. 2% and 92. 3% showed positive cells less than 30%, however, only 7.7% well differentiated patients showed positive cells less than 30 %, indicating low PDCD4 level was associated with histological grade, P〈0. 01. There is no relationship between PDCD4 expression and other clinicopathological parameters including sex, age and TNM status. CONCLUSION: Progressive down-regulation of PDCD4 in gastric cancer is correlated with histological grade. PDCD4 may play an important role in occurrence and development of gastric cancer.
出处 《中华肿瘤防治杂志》 CAS 2006年第7期481-484,共4页 Chinese Journal of Cancer Prevention and Treatment
基金 国家自然科学基金资助(30371625)
关键词 胃肿瘤/病理学 免疫组织化学 肿瘤蛋白质类/分析 stomach neoplasms/pathology immunohistochemistry neoplasm proteins/analytical
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参考文献10

  • 1Chen Y, Knosel T, Kristiansen G, et al. Loss of PDCD4 expression in human lung cancer correlates with tumor progression and prognosis[J]. J Pathol, 2003, 200(5): 640-646.
  • 2Yoshinaga H, Matsuhashi S, Fujiyama C, et al. Novel human PDCD4 (H731) gene expressed in proliferative cells is expressed in the small duct epithelial cells of the breast as revealed by an anti-H731 antibody[J]. Pathol Int, 1999, 49(12): 1067-1077.
  • 3李连弟,鲁凤珠,张思维,牧人,孙秀娣,皇甫小梅,孙杰,周有尚,欧阳宁慧,饶克勤,陈育德,孙爱明,薛志福,夏毅.中国恶性肿瘤死亡率20年变化趋势和近期预测分析[J].中华肿瘤杂志,1997,19(1):3-9. 被引量:869
  • 4吕有勇.多基因变异的累积与肿瘤发生发展的关系[J].中华医学杂志,1997,77(11):877-880. 被引量:17
  • 5Soejima H, Miyoshi O, Yoshinaga H, et al. Assignment of the programmed cell death 4 gene (PDCD4) to human chromosome band 10q24 by in situ hybridization[J]. Cytogenet Cell Genet,1999, 87(1-2): 113-114.
  • 6Matsuhashi S, Yoshinaga H, Yatsuki H, et al. Isolation of a novel gene from a human cell line with Pr-28 mAb which recognizes a nuclear antigen involved in the cell cycle[J]. Res Comm Biochem Cell Mol Biol, 1997, 1(1): 109-120.
  • 7Yoshinaga H, Matsuhashi S, Ahanek J, et al. Expression and identification of H731 gene product in HeLa cells[J]. Res Commun Biochem Cell Mol Biol, 1997, 1(1): 121-131.
  • 8Lankat-Buttgereit B, Goke R. Programmed cell death protein 4 (pdcd4): a novel target for antineoplastic therapy? [J]. Biol Cell, 2003, 95(8): 515-519.
  • 9Yang H S, Knies J L, Stark C, et al. Pded4 suppresses tumor phenotype in JB6 cells by inhibiting Ap-1 transactivation[J].Oncogene, 2003, 22(24): 3712-3720.
  • 10Goke A, Goke R, Knolle A, et al. DUG is a novel homologue of translation initiation factor 4G that binds eIF4A[J]. Bioehem Biophys Res Commun, 2002, 297(1): 78-82.

二级参考文献24

  • 1崔建涛,北京医科大学学报,1995年,27卷,33页
  • 2高崇峰,中华医学杂志,1995年,75卷,558页
  • 3吕有勇,中华医学杂志,1995年,75卷,679页
  • 4张青云,中华医学杂志,1995年,75卷,679页
  • 5李诤,中华肿瘤杂志,1995年,17卷,增刊,33页
  • 6吕有勇,Chin J Cancer Res,1994年,6卷,149页
  • 7吕有勇,Gemes Chromosom Cancer,1994年,9卷,76页
  • 8Deng G R,Semin Surg Oncol,1994年,10卷,83页
  • 9Li J Y,Semin Surg Oncol,1994年,10卷,95页
  • 10杨定成,北京医科大学学报,1994年,26卷,102页

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