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胰腺癌组织中血管内皮生长因子mRNA与尿激酶型纤溶酶原激活物mRNA定量表达的临床意义分析

席鹏程 时开网 朱响 杨坤兴 刘子君 卞建民 赵有财

引用本文:
Citation:

胰腺癌组织中血管内皮生长因子mRNA与尿激酶型纤溶酶原激活物mRNA定量表达的临床意义分析

DOI: 10.3969/j.issn.1001-5256.2014.08.014
基金项目: 

南京市卫生局资助课题(YKK09067); 

详细信息
  • 中图分类号: R735.9

Analysis of clinical significance of quantitative expression of VEGF mRNA and uPA mRNA in pancreatic cancer tissue

Research funding: 

 

  • 摘要: 目的探讨胰腺癌组织中血管内皮生长因子(VEGF)mRNA、尿激酶型纤溶酶原激活物(uPA)mRNA定量表达的临床意义。方法自2008年1月至2011年12月于本科行胰头癌根治术的患者中筛选出经病理证实为导管腺癌的30例患者的完整资料,采用荧光定量PCR(qPCR)检测其胰腺癌组织及6例正常胰腺组织中VEGF mRNA、uPA mRNA定量表达,分析其与临床病理因素之间的关系。结果 VEGF mRNA、uPA mRNA的表达与胰腺癌的组织分化程度、神经侵犯有关。VEGF mRNA在淋巴结转移阳性组中的定量表达高于淋巴结转移阴性组,两组比较差异有统计学意义(t=20.007,P=0.000);uPA mRNA在直径≤2 cm的肿瘤组织中定量水平小于直径>2 cm的肿瘤组织,两组比较差异有统计学意义(t=7.539,P=0.000)。uPA mRNA在伴有十二指肠侵犯组中的定量表达高于无十二指肠侵犯组,两组比较差异有统计学意义(t=-2.089,P=0.037)。uPA mRNA在Ⅲ期肿瘤组织中的定量表达高于Ⅰ、Ⅱ期肿瘤组织中的定量表达,两组比较差异有统计学意义(t=-9.450,P=...

     

  • [1]XU KC.Investigation of treatment strategy for advanced cancer according to treatment of pancreatic cancer[J].J Clin Hepatol, 2013, 29 (7) :484-488. (in Chinese) 徐克成.从胰腺癌治疗探讨进展期癌症治疗策略[J].临床肝胆病杂志, 2013, 29 (7) :484-488.
    [2] JEMAL A, SIEGEL R, XU J, et al.Cancer statistics, 2010[J].CA Cancer J Clin, 2010, 60 (5) :277-300.
    [3]LEUNG DW, CACHIANES G, KUANG WJ, et al.Vascular endothelial growth factor is a secreted angiogenic mitogen[J].Science, 1989, 246 (4935) :1306-1309.
    [4]ZORGETTO VA, SILVEIRA GG, OLIVEIRA-COSTA JP, et al.The relationship between lymphatic vascular density and vascular endothelial growth factor A (VEGF-A) expression with clinicalpathological features and survival in pancreaticadenocarcinomas[J].Diagn Pathol, 2013, 8:170.
    [5]WEIDNER N.Tumoral vasculary as a prognostic factor in cancer patients:the evendence continues to grow[J].J Pathol, 1998, 184 (2) :119-122.
    [6]ROGERS A, SMITH MJ, DOOLAN P, et al.Invasive markers identified by gene expression profiling in pancreatic cancer[J].Pancreatology, 2012, 12 (2) :130-140.
    [7]HILDENBRAND R, NIEDERGETHMANN M, MARX A, et al.Amplification of theurokinasetype plasm inogen activator receptor (uPAR) gene in ductal pancreatic carcinomas identifies a clinically highrisk group[J].Am J Pathol, 2009, 174 (6) :2246-2253.
    [8]DOBRILA-DINTINJANA R, VANIS N, DINTINJANA M, et al.Etiology and oncogenesis of pancreatic carcinoma[J].Coll Antropol, 2012, 36 (3) :1063-1067.
    [9]ASUTHKAR S, STEPANOVA V, LEBEDEVA T, et al.Multifunctional roles of urokinase plasminogen activator (uPA) in cancer stemness and chemoresistance of pancreatic cancer[J].Mol Biol Cell, 2013, 24 (17) :2620-2632.
    [10]SCHLAEPI JM, WOOD JM.Targeting vascular endothelial growth factor (VEGF) for anti-tumor therapy, by anti-VEGF neutralizing monoclonal antibodies or by VEGF receptor tyrosine-kinase inhibitors[J].Cancer Metastasis Res, 1999, 18 (4) :473-481.
    [11]NIETHAMMER AG, LUBENAU H, MIKUS G, et al.Doubleblind, placebo-controlled first in human study to investigate an oral vaccine aimed to elicit an immune reaction against the VEGFReceptor 2 in patients with stage IV and locally advanced pancreatic cancer[J].BMC Cancer, 2012, 12:361.
    [12]HBEL S, KOBURGER I, JOHN M, et al.Polyethylenimine/small interfering RNA-mediated knockdown of vascular endothelial growth factor in vivo exerts anti-tumor effects synergistically with Bevacizumab[J].J Gene Med, 2010, 12 (3) :287-300.
    [13]MARTIN LK, LI X, KLEIBER B, et al.VEGF remains an interesting target in advanced pancres cancer (APCA) :results of a multi-institutional phase II study of bevacizumab, gemicitabine, and infusional 5-fluorouracil in patients with APCA[J].Ann Oncol, 2012, 23 (11) :2812-2820.
    [14]HILEY CT, CHARD LS, GANGESWARAN R, et al.Vascular endothelial growth factor A promotes vaccinia virus entry into host cells via activation of the Akt pathway[J].J Virol, 2013, 87 (5) :2781-2790.
    [15]KINDLER HL, NIEDZWIECKI D, HOLLIS D, et al.Gemcitabine plus bevacizumab compared with gemcitabine plus placebo in patients with advanced pancreatic cancer:phaseⅢtrial of the Cancer and Leukemia Group B (CALGB 80303) [J].J Clin Oncol, 2010, 28 (22) :3617-3622.
    [16]VAN CUTSEM E, VERVENNE WL, BENNOUNA J, et al.PhaseⅢtrial of bevacizumab in combination with gemcitabine and erlotinib in patients with metastatic pancreatic cancer[J].J Clin Oncol, 2009, 27 (13) :2231-2237.
    [17]LU JD.Novel therapeutic strategies for advanced pancreatic cancer:targeting the epidermal growth factor and vascular endothelial growth factor pathways[J].China Oncol, 2009, 19 (8) :590-596. (in Chinese) 陆嘉德.晚期胰腺癌的分子靶向治疗[J].中国癌症杂志, 2009, 19 (8) :590-596.
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  • 收稿日期:  2014-05-16
  • 出版日期:  2014-08-20
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