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1.
目的 探讨血清血管内皮生长因子(vascular endothelial growth factor,VEGF)、血小板衍生生长因子(platelet-derived growth factor,PDGF)和表皮生长因子受体(epidermal growth factor receptor,EGFR)测定在非小细胞肺癌(non-small cell lung cancer,NSCLC)诊断和预后判定中的意义.方法 采用双抗体夹心ABC-ELISA法测定31例NSCLC患者及30名健康者血清VEGF、PDGF和EGFR的含量.结果 NSCLC患者血清VEGF、PDGF和EGFR测定值均高于健康对照组(P值均<0.01).血清VEGF、PDGF和EGFR测定值与NSCLC病理分型无关(P值均>0.05),与远处转移有关,远处转移组的测定值高于未转移组(P<0.05~0.01).NSCLC患者血清VEGF与PDGF测定值之间呈显著正相关(r=0.641,P<0.01),血清VEGF和EGFR测定值呈正相关(r=0.369,P<0.05).结论 检测血清VEGF、PDGF和EGFR水平对NSCLC的诊断和预后判定具有一定价值.  相似文献   

2.
目的探讨分泌转化生长因子-β、血小板衍生生长因子、血管内皮生长因子在特发性肺纤维化(IPF)患者支气管肺泡灌洗液(BALF)和血清中的表达水平及评估病情进展的临床意义。 方法选择2014年1月至2018年12月在我院呼吸科诊治的35例IPF患者作为观察组,18例肺结节病患者(Ⅰ期)作为对照组;采用免疫印迹观察TGFβ1、PDGF、VEGF在IPF患者血清中是否存在表达;用酶联免疫吸附法(ELISA)观察2组患者BALF和血清中TGFβ1、PDGF、VEGF的表达水平;最后分析IPF患者BALF和血清中TGFβ1、PDGF、VEGF表达水平与肺功能及血氧饱和度的相关性。 结果TGFβ1、PDGF、VEGF细胞印在IPF患者血清存在表达;与对照组相比,BALF及血清中的TGFβ1、PDGF、VEGF表达上调(P<0.05);IPF组患者BALF及血清中TGFβ1、PDGF、VEGF表达水平与肺功能中FVC%、FEV1%和DLCO%呈负性相关(P<0.05);与血氧饱和度也呈显著负相关(P<0.05)。 结论IPF患者BALF和血清中TGFβ1、PDGF、VEGF的表达水平明显升高;TGFβ1、PDGF、VEGF与患者的肺功能及血氧饱和度呈负相关,可作为评估IPF患者病情的临床评价指标。  相似文献   

3.
目的 观察风湿性心脏病心房颤动患者心房组织中肝细胞生长因子(HGF)、结缔组织生长因子(CTGF)、转化生长因子(TGF)-β1基因表达的变化.方法 35例行心脏手术者于术中获取的右心耳(约200 mg)分为3组,风湿性心脏病27例,其中窦性心律者8例,慢性持续性心房颤动者19例(≥16个月),分别列为风湿性心脏病窦性心律组和风湿性心脏病心房颤动组,另先天性心脏病患者8例(均为窦性心律)作为对照组,以β-肌动蛋白为内参照基因,通过实时荧光定量聚合酶链反应(real time PCR)技术,测定各组心房组织中HGF、CTGF、TGF-β1与Ⅰ型和Ⅲ型胶原mRNA的含量,苏木素-伊红(HE)和Massom病理染色观察右心耳组织纤维化程度.结果 与对照组比较,CTGF、TGF-β1、Ⅰ型胶原、Ⅲ型胶原mRNA表达在风湿性心脏病窦性心律组和风湿性心脏病心房颤动组均显著增加(P<0.05),且风湿性心脏病心房颤动组与风湿性心脏病窦性心律组比较也明显增加(P<0.05);HGF在风湿性心脏病窦性心律组较对照组增加,但比较差异无统计学意义,而在风湿性心脏病心房颤动组HGF下降明显,与对照组和风湿性心脏病窦性心律组比较差异均有统计学意义(P<0.05);相关性分析显示风湿性心脏病心房颤动患者心房组织Ⅰ型胶原、Ⅲ型胶原、TGF-β1和CTGF的mRNA表达与左房直径和组织纤维化面积有相关性.结论 风湿性心脏病患者Ⅰ型胶原和Ⅲ型胶原mRNA表达增加,CTGF、TGF-β1mRNA表达上调.具有抗纤维化作用的HGF mRNA表达在心房颤动时下降,可能是使得风湿性心脏病患者心房颤动易于发生和维持的重要原因.  相似文献   

4.
胃癌组织与血清中VEGF和bFGF的表达意义   总被引:1,自引:3,他引:1  
目的:研究胃癌患者血清和组织中VEGF,bFGF的表达与胃癌临床特征之间的关系,研究二者的相关性及组织和血清之间的相关性,探讨VEGF,bFGF在胃癌的发生、发展、侵袭和转移中的作用方法:应用酶联免疫技术(ABC-ELISA方法)检测73例胃癌患者术前血清和20例健康体检者血清中的VEGF,bFGF的表达水平,同时应用免疫组织化学染色方法检测癌组织和癌旁组织中VEGF,bFGF的表达.结果:胃癌患者术前血清VEGF,bFGF表达水平均明显高于健康体检者(YEGF:101.8±53.3 ng/L vs 16.1±22.5ng/L,P<0.05;bFGF:152.9±42.7ng/L vs 25.0±11.4ng/L,P<0.05).胃癌患者术前血清VEGF,bFGF的表达水平均随胃癌的浸润深度、TNM分期、淋巴结转移、远处转移而增高(P<0.05),而与年龄、性别及病理类型无关.胃癌组织VEGF的阳性表达率为71.2%,癌旁组织中VEGF均未见阳性表达,二者之间有显著性差异(X~2=32.1,P<0.05);胃癌组织中bFGF的阳性表达率为63.0%、癌旁组织中bFGF阳性表达率为(10%),二者之间亦有显著性差异(X~2=17.7,P<0.05).胃癌患者组织VEGF,bFGF的表达水平均与胃癌的浸润深度、TNM分期、淋巴结转移、远处转移有关(P<0.05),而与年龄、性别及病理类型无关.胃癌患者血清VEGF的表达水平与血清bFGF的表达水平呈明显正相关(r=0.439,P<0.01),胃癌患者组织VEGF的表达水平与组织bFGF的表达水平呈明显正相关(r=0.391,P<0.01);胃癌患者术前血清VEGF的表达水平与组织VEGF的表达呈正相关(r=0.346,P<0.01),术前血清bFGF的表达水平与组织bFGF的表达呈正相关(r=0.304,P<0.01),均有显著性差异.结论:VEGF,bFGF在胃癌的发生、发展、转移及预后起着重要的作用,有望成为胃癌术前诊断、术后随访、复发转移监测、评价抗血管生成药物疗效和化疗效果判定的新的肿瘤标志物.  相似文献   

5.
Summary The in vitro growth requirements of three human embryonal carcinoma cell lines (H 12.7, 2102 EP, 1428 A) were investigated. The basal medium DME/F12 supplemented with insulin, transferrin, and low-density and high-density lipoproteins was sufficient to support substantial multiplication of all three lines. The most efficient attachment factor was either fibronectin (for 2102 EP and 1428 A) or collagen type I (H 12.7). In a serum-free system the influence of epidermal growth factor (EGF), insulin-like growth factor I, multiplication stimulating activity (MSA), a platelet extract, and the glucocorticoids dexamethasone and hydrocortisone, as determined by the DNA synthesis rate of the cells, was generally minimal. However, the DNA synthesis rate of cell lines H 12.7 and 2102 EP was increased by MSA, and the line with the highest potential to differentiate (H 12.7) was stimulated by EGF. All three cell lines secreted growth factors in a heterologous stimulation assay. Insulin-like growth factors I and II were not part of the growth promoting activity. The inhibitory effect of a monoclonal anti-EGF antibody on the 3H-thymidine incorporation of cell line 2102 EP might indicate autocrine secretion of EGF or an EGF-like factor by this cell line.  相似文献   

6.
ABSTRACT— Expression of epidermal growth factor (EGF) and fibroblast growth factor (FGF) was examined in 56 patients with hepatocellular carcinoma (HCC) using an immunohistochemical method. EGF and FGF were expressed on carcinoma cells in 14 (25%) and 23 cases (41%), respectively. In the 23 FGF-positive cases, 11 cases were positive for both acidic and basic FGF, while 18 were positive for acidic FGF, and 16 were positive for basic FGF. In non-cancerous hepatic tissues, FGF was weakly positive in macrophages, hepatocytes and vascular endothelial cells in some cases, while EGF was totally negative. There were no significant correlations between the expression of EGF or FGF on carcinoma cells and the various clinicopathologic factors examined. These data suggest that EGF and FGF are produced by human HCC cells in vivo. The roles of the expression of these growth factors in the development and progression of HCC remain only speculative.  相似文献   

7.
Angiogenesis is a crucial process in the progression of multiple myeloma (MM). Vascular endothelial growth factor (VEGF) and hepatocyte growth factor (HGF) are multifunctional cytokines that potently stimulate angiogenesis including tumour neovascularization. Serum levels of VEGF and HGF were measured in 52 patients with MM by enzyme-linked immunosorbent assay (ELISA). Serum levels of VEGF and HGF were elevated in MM patients compared with healthy controls (VEGF: mean 0.31 ng/ml and 0.08 ng/ml respectively, P < 0.01; HGF: mean 2.17 ng/ml and 0.45 ng/ml, respectively, P < 0.001). In serial samples taken after chemotherapy, serum VEGF and HGF levels were correlated with M-protein levels. Serum levels of VEGF were higher in patients with extramedullary plasmacytomas than in patients without them (P < 0.05). They were also significantly higher in a group of patients who showed poor response to chemotherapy (P < 0.01). Serum levels of HGF were higher in patients with complications such as anaemia, hypercalcaemia and amyloidosis than in patients without these complications (P < 0.01, P < 0.05, P < 0.05 respectively). Both serum VEGF and HGF levels were significant predictors of mortality (P = 0.01, P = 0.02, respectively, log-rank test). The present study demonstrated that serum levels of VEGF and HGF are significantly elevated and dependent on the severity of MM, suggesting that measurement of VEGF and HGF may be useful for assessing disease progression and for predicting the response to chemotherapy in MM patients.  相似文献   

8.
目的:研究非霍奇金淋巴瘤(NHL)患者血清血管内皮生长因子(sVEGF)及血清碱性成纤维细胞生长因子(sbFGF)水平与临床特征的关系,探索其临床意义.方法:ELISA法检测36例不同病期NHL患者sVEGF、sbFGF水平,并收集临床资料,进行统计分析.结果:NHL患者sVEGF、sbFGF水平明显高于对照组(均P<...  相似文献   

9.
目的 观察碱性成纤维细胞生长因子 (b FGF)和血管内皮生长因子 (VEGF)与动脉粥样硬化 (AS)的关系 ,以及卡托普利 (captopril)对 AS和 b FGF、VEGF表达的影响。方法  36只兔随机分为 3组 :空白对照组 ( 组 )动物喂饲普通颗粒饲料 ;实验对照组 ( 组 )动物喂饲含 1g/d胆固醇和 3%猪油的饲料 ;实验组 ( 组 )喂饲含 1g/d胆固醇和 3%猪油的饲料 ,同时给予卡托普利 10 mg.kg- 1 .d- 1 。于 12周后处死动物 ,取出主动脉做 b FGF和 VEGF免疫组化定性和定量观察。结果 光镜下 组和 组有明显 AS形成。定量研究 :与 I组相比 , 组和 组 b FGF在主动脉内中膜的表达面积 (μm2 ) (2 6 999.6 8± 9931.82 ,2 4 0 75 .6 2± 2 4 787.6 8对 1386 8.14± 3180 .13)、密度 (5 .4 3±1.6 5 ,3.33± 1.15对 2 .0 7± 0 .78)和密度指数 (15 7886 .4 6± 113340 .0 5 ,73348.6 0± 4 6 0 4 8.81对 2 92 90 .78±15 0 16 .5 8)均有非常显著性增加 (P<0 .0 1) ,但 组与 组相比 ,其 b FGF表达的面积、密度和密度指数均有非常显著性降低 (P<0 .0 1)。与 组相比 , 组和 组 VEGF在主动脉内中膜的表达面积 (30 4 2 5 .4 3± 11114 .14 ,2 55 2 9.31± 10 30 5 .88对 1386 8.14± 3180 .13)、密度 (6 .10± 2 .0 9,6 .10± 2 .  相似文献   

10.
神经生长因子(nerve growth factor,NGF)对神经细胞的生长、分化、存活、维持均起着重要作用,NGF还通过调节多种免疫细胞,促进炎性介质释放,导致气道炎症,诱导神经元可塑性.NGF水平在支气管哮喘患者血清、痰液、支气管肺泡灌洗液、支气管黏膜中均有明显升高.本文就NGF的生物学特征、调节以及与支气管哮喘的3个主要特征气道炎症、气道高反应性和气道重塑的关系作一综述.  相似文献   

11.
目的:探讨碱性成纤维细胞生长因了(bFGF)和转化生长因子β1(TGFβ1)在人体超负荷性心肌肥厚发生机制中的作用。方法:用天狼猩红、免疫组织化学及原位杂交技术检测了32例肥大心肌(左、右心室心肌各16例)组织中胶原、bFGF和TGFβ1mRNA和蛋白的表达情况。结果:压力和容量超负荷都可使心肌组织胶原增生,bFGF、TGFβ1 mRNA和蛋白表达水平显著增加。bFGF、TGFβ1 mRNA和蛋白表达水平与心肌细胞横径增加呈显著正相关,TGFβ1 mRNA和蛋白表达水平与心肌胶原总量也呈显著正相关。结论:bFGF和TGFβ1表达可能是介导人体超负荷性心肌肥厚发生的因素之一。  相似文献   

12.
OBJECTIVES: To assess the association between total insulinlike growth factor (IGF)‐1, IGF binding protein‐1 (IGFBP‐1), and IGFBP‐3 levels and functioning and mortality in older adults. DESIGN: Cohort study. SETTING/PARTICIPANTS: One thousand one hundred twenty‐two individuals aged 65 and older without prior cardiovascular disease events participating in the Cardiovascular Health Study. MEASUREMENTS: Baseline fasting plasma levels of IGF‐1, IGFBP‐1, and IGFBP‐3 (defined as tertiles, T1‐T3) were examined in relationship to handgrip strength, time to walk 15 feet, development of new difficulties with activities of daily living (ADLs), and mortality. RESULTS: Higher IGFBP‐1 predicted worse handgrip strength (P‐trendT1‐T3<.01) and slower walking speed (P‐trendT1‐T3=.03), lower IGF‐1 had a borderline significant association with worse handgrip strength (P‐trendT1‐T3=.06), and better grip strength was observed in the middle IGFBP‐3 tertile than in the low or high tertiles (P=.03). Adjusted for age, sex, and race, high IGFBP‐1 predicted greater mortality (P‐trendT1‐T3<.001, hazard ratio (HR)T3vsT1=1.48, 95% confidence interval (CI)=1.15–1.90); this association was borderline significant after additional confounder adjustment (P‐trendT1‐T3=.05, HRT3vsT1=1.35, 95% CI=0.98–1.87). High IGFBP‐1 was associated with greater risk of incident ADL difficulties after adjustment for age, sex, race, and other confounders (P‐trendT1‐T3=.04, HRT3vsT1=1.40, CI=1.01–1.94). Neither IGF‐1 nor IGFBP‐3 level predicted mortality or incident ADL difficulties. CONCLUSION: In adults aged 65 and older, high IGFBP‐1 levels were associated with greater risk of mortality and poorer functional ability, whereas IGF‐1 and IGFBP‐3 had little association with these outcomes.  相似文献   

13.
目的:观察并分析肝细胞生长因子(HGF)及其受体c-Met与表皮生长因子受体(EGFR)在溃疡性结肠炎(UC)活动和非活动阶段患者结肠黏膜的表达情况,探讨其表达的临床意义.方法:根据改良Williams疾病活动指数(DAI) 将42例UC患者分为活动期(n=25)和非活动期(n=17)2组,对照组(n=20)为门诊健康体检者或肠易激综合征患者.结肠镜下活检各组患者结肠黏膜组织,采用免疫组化SABC法检测各组患者结肠黏膜HGF及c-Met表达;SP法检测EGFR及增殖细胞核抗原(PCNA)表达.结果:对照组、活动期UC患者、非活动期 UC患者HGF阳性表达率分别为22%,88%, 100%(X2=62.84,P<0.01);c-Met阳性表达率分别为25%,92%,100%(X2=62.34,P<0.01); EGFR阳性表达率分别为25%,92%,1 00%(X2 =54.34,P<0.01);PCNA过表达率分别为0, 36%,100%(X2=67.50,P<0.01),组间比较差异显著.HGF,c-Met和EGFR在UC患者结肠黏膜表达与PCNA过表达正相关(r=0.648,0.645, 0.565,P<0.01).结论:HGF,c-Met,EGFR及PCNA在非活动期UC患者结肠黏膜中的表达较活动期UC患者和对照组明显增加.HGF及其受体c-Met与 EGFR在UC患者结肠炎症黏膜修复过程中可能起一定作用.  相似文献   

14.
Vascular endothelial growth factor (VEGF) and hepatocyte growth factor (HGF) are thought to stimulate endothelial cell proliferation and induce angiogenesis in vivo. However, the precise mechanism responsible for VEGF and HGF release in patients with coronary artery disease is still unknown. We studied serum concentrations of VEGF and HGF in 20 patients with acute myocardial infarction (AMI), 20 patients with stable angina pectoris (AP) who had reversible perfusion defects on stress myocardial scintigraphy, and 16 patients with old myocardial infarction (OMI) who had no reversible defects on stress myocardial scintigraphy. The control group consisted of 20 patients with atypical chest pain who had angiographically normal coronary arteries. Serum VEGF and HGF concentrations were measured by enzyme-linked immunosorbent assay. Both the serum VEGF and HGF concentrations in the early stage of myocardial infarction in the patients with AMI were higher than those in the patients with AP and with OMI, and control patients. The VEGF concentration in the patients with AP was higher than in the patients with OMI, whereas the HGF concentration did not differ in the patients with AP and OMI. The VEGF concentration in AMI patients who had had preinfarction angina on admission was higher than that of patients who had had no preinfarction angina, whereas the HGF concentration did not differ between the two groups of patients. These results suggest that the serum VEGF concentration may reflect myocardial ischemia to a greater degree than the serum HGF concentration. Received June 9, 2000 / Accepted September 30, 2000  相似文献   

15.
Objective:To observe the preventive and control effect of matrine on transforming growth factor(TCF- β1) and hepatocyte.growth factor(HCF) of liver fibrosis tissue in rals.Methods:A total of48 SD rats were randomly divided into A,B,C,D groups with 12 in each,group A as the normal control group and groups B.C,D as liver fibrosis models using composite modulus method with carbon tetrachloride(CCL_4).Group B was the model group,group C adopted γ— interferon lavage therapy in the second day of modeling,and group D adopted matrine lavage treatment,at 4 and8 weeks after treatment.Six rats were executed for detection of TGF- β1 and HGF,liver tissue histology and comparison fibrosis degree changes of rat liver tissue between groups.Results:Croups B,C,D showed a more significantly increased TCF- β1 at each time point compared with group A(P0.05);Group B showed a more significantly increased TGF- β1 than groups C and D at weeks 4 and 8(P0.05);group D showed a lowest level of TGF-β1,followed by groups C and B.HGF of group B decreased more significantly than A group at weeks 4 and 8(P0.05);HGF of groups C and D was significantly elevated at 4 and 8 weeks than groups A and B(P0.05),in which the group D showed the highest level of HGF.According to tissue histologic observation,rat liver tissue structure of group A was clear and normal,tissue structure of group B was destroyed with obvious fibrous tissue hyperplasia and fatty change of hepatic cells;groups C and D showed a slighter liver tissue damage,cell necrosis and connective tissue hyperplasia in collect abbacy than group B with a trend of obvious improvement.Conclusions:Matrine can reduce TGF- β1expression and enhance the activity of HGF,so as to realize the inhibition effect on liver fibrosis in rats.  相似文献   

16.
17.
TO THE EDITOR Angiogenesis consists of the sprouting of capillaries from pre-existing vessels[1]. It is well-known that tumor growth is angiogenesis-dependent. Vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF)stimulated vascular endothelial cell proliferation and are involved in the neoplastic angiogenesis of several types of tumors including those of the intestinal tract[1-5].  相似文献   

18.
血管内皮细胞生长因子与治疗性血管新生   总被引:3,自引:0,他引:3  
本文概述了血管内皮细胞生长因子(VEGF)家族及其受体的组成,介绍了调控VEGF表达的因素及VEGF信号传导途径。着重阐述了VEGF促血管新生的作用机制,以及VEGF在治疗性血管新生中的研究与应用现状、存在问题及未来发展前景。还简要介绍了VEGF其他的生物学作用。  相似文献   

19.
Cholangiocarcinoma is a hepatic biliary cancer of high morbidity and mortality, whose molecular pathogenesis is unknown. However, there is increasing evidence to suggest that alterations in selected growth factor pathways, including an overexpression of the growth factor receptor tyrosine kinases c-ErbB-2/c-Neu and c-Met, together with possible aberrant autocrine expression of hepatocyte growth factor/scatter factor, the ligand for c-Met, may be playing important roles associated with the development of cholangiocarcinoma in both the human liver and in the furan rat model of cholangiocarcinogenesis. Cyclo-oxygenase-2, whose regulation has been experimentally related to c-ErbB-2/c-Neu as well as to hepatocyte growth factor/scatter factor, and which has been demonstrated to be overexpressed in other cancers of the gastrointestinal tract, has also been observed in preliminary studies to be upregulated in human biliary cancers and in cholangiocarcinoma induced in the furan rat model. Moreover, new data from our laboratory have demonstrated the cyclo-oxygenase-2 inhibitor NS-398 to produce a significant dose-dependent growth inhibition of rat cholangiocarcinoma cells in vitro, as well as to suppress anchorage-independent growth of these cells in soft agar. Based on the data reviewed, we propose that the selective therapeutic targeting of aberrant growth factor receptor tyrosine kinase signaling and of cyclo-oxygenase-2, alone or in combination, has potential to become a useful new approach for the treatment and/or chemoprevention of cholangiocarcinoma. We further propose that the furan rat model may serve as a powerful preclinical model for testing therapeutic and chemopreventative strategies that selectively target c-ErbB-2/c-Neu, cyclo-oxygenase-2, and/or autocrine hepatocyte growth factor/c-Met, aberrantly expressed in cholangiocarcinogenesis.  相似文献   

20.
碱性成纤维细胞生长因子(basic fibroblast growth factor,b-FGF)是一种肝素黏合多肽,具有促进细胞增殖、分化和黏附作用等多种细胞生物学活性.近年来研究表明b-FGF与支气管哮喘(简称哮喘)气道重塑的关系密切.目前,哮喘的发病机制仍不是很清楚,治疗方法也在探索中,b-FGF的研究有可能为研究哮喘发病机制及治疗提供新的亮点.  相似文献   

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