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胃癌肝转移患者治疗过程中血管内皮细胞生长因子水平的变化 被引量:2

Change of plasma VEGF level in gastric cancer patients with liver metastasis after chemotherapy
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摘要 目的:检测胃癌肝转移患者治疗前后的血浆可溶性血管内皮细胞生长因子(VEGF)水平,并探讨其临床意义。方法:采用定量酶联免疫吸附试验双抗体夹心法检测43例胃癌肝转移患者治疗前后和20例浅表性胃炎患者(对照组)的血浆可溶性VEGF水平。结果:胃癌肝转移患者血浆可溶性VEGF水平显著高于对照组。经治疗后病情好转的胃癌肝转移患者[疗效评价为完全缓解(CR)或部分缓解(PR)],其血浆可溶性VEGF水平较治疗前明显下降,两者之间的差异有统计学意义(P<0.05)。治疗后病情进展的胃癌肝转移患者[疗效评价为疾病进展(PD)],其血浆可溶性VEGF水平较治疗前明显升高,两者之间的差异有统计学意义(P<0.05)。在经治疗后病情稳定的胃癌肝转移患者[疗效评价为疾病稳定(SD)],其血浆可溶性VEGF水平与治疗前的差异无统计学意义。结论:用ELISA方法检测血浆可溶性VEGF浓度对于评价胃癌肝转移的治疗疗效有一定的参考价值。 Objective: To detect plasma vascular endothelial growth factor(VEGF) in gastric carcinoma patients with liver metastasis and investigate its significance in chemotherapy.Methods: Plasma levels of VEGF in 43 gastric cancer patients and 20 superficial gastritis patients were detected by ELISA test.Results: Plasma levels of VEGF in gastric carcinoma patients were found to be higher than those in gastritis patients.The plasma levels of VEGF in complete response(CR) or partial response(PR) gastric cancer patients decreased significantly after chemotherapy(P 0.05).However,the plasma VEGF did not differ significantly in stable disease(SD) gastric cancer patients although they were given the same treatment.In progressive disease(PD) patients,the plasma VEGF increased after the treatment.Conclusion: The plasma VEGF level determined by ELISA could be a reference for evaluating the efficacy of treatment and progression of illness for gastric cancer patients with liver metastasis.
出处 《南京医科大学学报(自然科学版)》 CAS CSCD 北大核心 2011年第11期1653-1655,共3页 Journal of Nanjing Medical University(Natural Sciences)
关键词 胃癌 血管内皮细胞生长因子 酶联免疫吸附试验双抗体夹心法 化疗 stomach neoplasms vascular endothelial growth factor ELISA chemotherapy
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  • 1王文欢,伍仁毅,孙国瑛,李新华,袁伟建,唐丽安.VEGF-C和VEGF-D在胃癌组织中的表达与淋巴结转移的关系[J].中南大学学报(医学版),2010,35(4):335-340. 被引量:18
  • 2Iordache S,Saftoiu A,Georgescu CV,et al. Vascular endothelial growth factor expression and microvessel density-two useful tools for the assessment of prognosis and survival in gastric cancer patients[J]. Gastrointestin Liver Dis, 2010,19(2) : 135-139.
  • 3Hanahan D,Weinberg RA. The hallmarks of cancer[J].Cell, 2000,100( 1 ) : 57-70.
  • 4Robbins PF,Morgan RA, Feldman SA,et al. Comparison of doxorubicin-eluting bead transarterial chemoembolization (DEB-TACE) with conventional transarterial chemo- embolization (TACE) for the treatment of hepatoeellular carcinoma[J]. Radioloqia,2011,53(3) :246-253.
  • 5Hicklin DJ,Ellis LM. Role of the vascular endothelial growth factor pathway in tumer growth and angiogenesis [J]. J Clin Oncol,2005,23(5): 1011-1027.
  • 6Pan Q, Chanthery Y,Liang WC,et al. Blocking neropilin - 1 function has an additive effect with anti-VEGF to inhibit tumor growth[J]. Cancer Cell, 2007, 11 ( 1 ) : 53-67.
  • 7Robert R Jr. Vascular endothelial growth factor (VEGF) signaling in tumor progression[J]. Crit Rev Oncol Hematol, 2007,62(3) : 179-213.
  • 8Lieto E, Ferraccio F, Orditura M, et al. Expression of vascular endothelial growth factor (VEGF) and epidermal growth factor receptor(EGFR) is an independent prognostic indicator of worse outcome ingastric cancer patients [J]. An Surg Oncol,2007,15(1) :69-79.
  • 9Ma J,Sawai H,Matsuo Y,et al. Interleukin - lα enhances angiogenesis and is associated with liver matastatic potential in human gastric cancer cell lines, [J]. J Surg Res, 2008,148(2) : 197-204.
  • 10Zhang J, JI J,Yuan F, et al. Cyclooxygenase-2 expression is associated with VEGF-C and lymph node metastases in gastric cancrer patients [J]. Biomed Pharma,2005,59 (Suppl 2) :$285-288.

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  • 1Filipowicz W,Bhattachary. ya SN,Sonenberg N. Mecha- nisms of post-transcriptional regulation by microRNAs: are the answers in sight? [J]. Nat Rev Genet,2008,9 (2) : 102-114.
  • 2Zhang Y, Li M, Wang H, et al. Profiling of 95 microRNAs in pancreatic cancer cell lines and surgical specimens by real-time PCR analysis [Jl- World J Surg,2009,33(4): 698-709.
  • 3Liu B,Peng XC,Zheng XL,et al. MiR-126 restoration down-regulate VEGF and inhibit the growth of lung can- cer cell lines in vitro and in vivo [J]. Lung Cancer, 2009,66(2) : 169-175.
  • 4Li JM,Zhao RH,Li ST,et al. Down-regulation of fecal miR-143 and miR-145 as potential markers for colorectal cancer[J]. Saudi Med J, 2012,33 (1) : 24-29.
  • 5Ventura A, Jacks T. MicroRNAs and cancer:short RNAs go a long way[J]. Cell,2009,136(4) :586-591.
  • 6Murakami Y,Yasuda T,Saigo K,et al. Comprehensive analysis of microRNA expression patterns in hepatocellu- lar carcinoma and non-tumorous tissues [J]. Oncogene, 2006,25 (17) : 2537-2545.
  • 7Law PT, Wong N. Emerging roles of microRNA in the in- tracellular signaling networks of hepatocellular carcinoma [ J ]. J Gastroenterol Hepatol, 2011,26 (3) : 437-449.
  • 8Guan Y,Yao H,Zheng Z,et al. MiR-125b targets BCL3 and suppresses ovarian cancer proliferation [J]. Int J Cancer, 2011,128(10) : 2274-2283.
  • 9Liang L,Wong CM,Ying Q,et al. MicroRNA-125b sup- pressesed human liver cancer cell proliferation and metastasis by directly targeting oncogene LIN28B2 [J]. Hepatology,2010,52(5) : 1731-1740.
  • 10Heneghan HM, Miller N, Kerin MJ. MiRNAs as biomark- ers and therapeutic targets in cancer[J]. Curr Opin Phar- maeol, 2010,10(5) : 543-550.

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