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基质金属蛋白酶-9、血管内皮生长因子和增殖细胞核抗原在胃腺癌表达的相关性及临床意义 被引量:4

The relationship of MMP-9, VEGF and PCNA expressions and their clinical significance in gastric adenocarcinoma
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摘要 目的研究胃腺癌中基质金属蛋白酶-9(MMP-9)及其相关因子血管内皮生长因子(VEGF)和增殖细胞核抗原(PCNA)蛋白的表达,并分析其临床意义。方法利用组织芯片技术,通过免疫组化法检测45例胃腺癌组织及其相应的45例癌旁组织和10例正常胃黏膜组织中MMP-9、VEGF和PCNA蛋白的表达,并分析它们的相关性及其与胃腺癌的分化程度和发生发展的关系。结果本研究中MMP-9、VEGF和PCNA分别在胃腺癌、癌旁组织、正常胃黏膜中检出的阳性率为:MMP-9,82.2%(37/45)、64.4%(29/45)、30.0%(3/10),差异有统计学意义(P=0.019);VEGF,73.3%(33/45)、62.2%(28/45)、30.0%(3/10),差异有统计学意义(P=0.029);PCNA,84.4%(38/45)、71.1%(32/45)、10.0%(1/10),差异有统计学意义(P=0.001)。MMP-9、VEGF和PCNA分别在高、中、低分化胃腺癌组织中的阳性率为:MMP-9,70.0%(7/10)、80.0%(8/10)、88.0%(22/25),差异有统计学意义(P=0.015);VEGF,50.0%(5/10)、60.0%(6/10)、88.0%(22/25),差异有统计学意义(P=0.000);PCNA,60.0%(6/10)、90.0%(9/10)、92.0%(23/25),差异有统计学意义(P=0.004)。等级相关分析表明MMP-9、VEGF和PCNA呈两两正相关(P〈0.05)。结论组织芯片技术是胃腺癌中各种蛋白表达的一种强有力的分析工具。MMP-9、VEGF和PCNA蛋白参与胃腺癌的发生发展过程,可以成为临床上评价预后的指标。 Objective To investigate abnormal protein expression of matrix metalloproteinase-9 (MMP-9) , vascular endothelial growth factor (VEGF) and proliferating cell nuclear antigen ( PCNA ) in human gastric adenocarcinoma, and further reveal the clinical significance. Method The MMP-9, VEGF and PCNA proteins expression was determined by immunohistochemistry staining in 45 gastric adenocarcinoma tissues, 45 adjacent specimens and 10 normal gastric mucosa tissues via tissue arrays accordingly. The relationship of these protein expression with differentiation degree, development and progression of gastric adenocarcinoma were also analyzed. Results Positive rates of MMP-9, VEGF and PCNA in gastric adenocarcinoma, adjacent specimens and gastric normal mueosa were as follows: MMP-9, 82. 2% (37/45), 64.4% (29/45), 30. 0% (3/10) (P =0.019); VEGF, 73.3% (33/45), 62. 2% (28/45), 30. 0% (3/10) ( P = 0. 029 ) ; PCNA, 84.4% ( 38/45 ), 71.1% ( 32/45 ), 10.0% ( 1/10 ), there were statistically significant difference( P = 0. 001 ). The positive rates of MMP-9, VEGF and PCNA in well- differentiated adenocarcinoma, moderately differentiated adenocarcinoma and poorly differentiated were as follows : MMP-9,70. 0% (7/10), 80. 0% ( 8/10 ), 88.0% (22/25), there were statistically significant difference (P =0. 015) ;VEGF, 50.0% (5/10), 60. 0% (6/10), 88. 0% (22/25), there were statistically significant difference ( P = 0. 000 ) ; PCNA, 60. 0% (6/10) ,90.0% (9/10), 92.0% (23/25) ,the difference is significant statistically (P = 0. 004 ). The expression of MMP-9, VEGF and PCNA showed positive relationship with each other by rank correlation analysis ( P 〈 0.05 ). Conclusion Tissue arrays technology is effective tool to analyze the expression of cancer related proteins in gastric adenocareinoma. The expression of MMP-9, VEGF and PCNA proteins participates in the tumorigenesis and development process of gastric adenocarcinoma, and these can be used as indexes to evaluate prognosis in clinical.
出处 《中华内科杂志》 CAS CSCD 北大核心 2009年第2期114-117,共4页 Chinese Journal of Internal Medicine
基金 天津市基础重点资助项目(07JCZDJC07700)
关键词 胃肿瘤 基质金属蛋白酶9 血管内皮生长因子类 增殖细胞核抗原 组织芯片技术 Stomach neoplasms Matrix metalloproteinase 9 Vascular endothelial growth factors Proliferating cell nuclear antigen Tissue arrays technology
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参考文献8

  • 1胡伟国,王春友,刘涛,熊炯邤,杨智勇.SHH、EGFR和PCNA蛋白在胰腺癌组织中的表达及其意义[J].癌症,2007,26(9):947-951. 被引量:7
  • 2Hamacher S, Matern S, Roeb E. Extracellular matrix from basic research to clinical significance. An overview with special consideration of matrix metalloproteinases. Dtsch Med Wochensehr, 2004 , 129 : 1976-1980.
  • 3Illemann M, Bird N, Majeed A, et al. MMP-9 is differentially expressed in primary human colorectal adenocarcinomas and their metastases. Mol Cancer Res, 2006,4:293-302.
  • 4Sun WH, Sun YL, Fang RN, et al. Expression of cyclooxygenase- 2 and matrix metalloproteinase-9 in gastric carcinoma and its correlation with angiogenesis. Jpn J Clin Oncol,2005 ,35 :707-713.
  • 5梁启廉,陈小东,王三明,李建文,黄冰,许燕云,陈雪松.VEGF和metastin在大肠癌组织中的表达[J].南方医科大学学报,2007,27(10):1584-1587. 被引量:15
  • 6Hollbom M, Stathopoulos C, Steffen A, et al. Positive feedback regulation between MMP-9 and VEGF in human RPE cells. Invest Ophthalmol Vis Sei ,2007,48:4360-4367.
  • 7Pregel P, Bollo E, Cannizzo FT, et al. Effect of anabolics on bovine granulosa-luteal cell primary cultures. Folia Histochem Cytobiol, 2007,45:265-271.
  • 8Czyzewska J, Guzinska-Ustymowicz K, Lebelt A, et al. Evaluation of proliferating markers Ki-67, PCNA in gastric cancers. Rocz Akad Med Bialymst, 2004,49:64-66.

二级参考文献24

  • 1郭桂芳,谢汝华,杨安奎,陈直华,吴秋良,刘巍巍,区深明,夏良平,陈明远,张晋昕.晚期上颌窦鳞癌组织中GST-π和PCNA的表达与预后的关系[J].癌症,2005,24(10):1267-1271. 被引量:2
  • 2Thayer S P, Di Magliano M P, Heiser P W, et al. Hedgehog is an early and late mediator of pancreatic cancer tumorigenesis [ J ]. Nature, 2003,425 (6960) : 851-856.
  • 3Buck E, Eyzaguirre A, Brown E, et al. Rapamycin synergizes with the epidermal growth factor receptor inhibitor erlotinib in non-small-cell lung, pancreatic, colon, and breast tumors [J]. Mol Cancer Ther, 2006,5( 11 ) :2676-2684.
  • 4Wang Z, Sengupta R, Banerjee S, et al. Epidermal growth factor receptor-related protein inhibits cell growth and invasion in pancreatic cancer [J]. Cancer Res, 2006,66(15):7653- 7660.
  • 5Sui G, Bonde P, Dhara S, et al. Epidermal growth factor receptor and hedgehog signaling pathways are active in esophageal cancer cells from rat reflux model [J]. J Surg Res, 2006, 134( 1 ) : 1-9.
  • 6Mimeault M, Moore E, Moniaux N, et al. Cytotoxic effects induced by a combination of cyclopamine and gefitinib, the selective hedgehog and epidermal growth factor receptor signaling inhibitors, in prostate cancer cells [J]. Int J Cancer, 2006, 118(4) : 1022-1031.
  • 7Amin A, Li Y, Finkelstein R. Hedgehog activates the EGF receptor pathway during Drosophila head development [J]. Development, 1999,126(12) :2623-2630.
  • 8Ahaba A, Stecca B, Sanchez P. Hedgehog-Gli signaling in brain tumors: stem cells and paradevelopmental programs in cancer [J]. Cancer Lett, 2004,204(2) : 145-157.
  • 9Beachy P A, Karhadkar S S, Berman D M. Tissue repair and stem cell renewal in carcinogenesis [J]. Nature, 2004,432 (7015) : 324-331.
  • 10Ruizi Altaba A, Sanchez P, Dahmane N. Gli and hedgehog in cancer: tumours, embryos and stem cells [J]. Nat Rev Cancer, 2002,2(5) :361-372.

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