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首页> 外文期刊>Journal of Hainan Medical University >Effect of continuous recombinant human endostatin pumping combined with TP chemotherapy on serum malignant molecules and angiogenesis molecules in patients with advanced ovarian cancer
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Effect of continuous recombinant human endostatin pumping combined with TP chemotherapy on serum malignant molecules and angiogenesis molecules in patients with advanced ovarian cancer

机译:连续重组人内皮抑素联合TP化疗对晚期卵巢癌患者血清恶性分子和血管生成分子的影响

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Objective: To study the effect of continuous recombinant human endostatin pumping combinedwith TP chemotherapy on serum malignant molecules and angiogenesis molecules in patientswith advanced ovarian cancer. Methods: 78 patients with advanced ovarian cancer who weretreated in our hospital between July 2011 and December 2015 were selected and divided intoobservation group and control group (n=39) according to the single-blind randomized controlmethod. Before treatment and after 4 cycles of treatment, electrochemical luminescenceimmunity analyzer was used to detect serum tumor marker levels; RIA method was used todetermine serum apoptosis molecule levels; enzyme-linked immunosorbent assay (ELISA)was used to detect the serum angiogenesis molecule levels. Results: Before treatment,differences in serum levels of tumor markers, apoptosis molecules and angiogenesis moleculeswere not statistically significant between two groups of patients (P0.05). After 4 cycles oftreatment, serum carbohydrate antigen 125 (CA125), carbohydrate antigen 153 (CA153),human epididymis protein 4 (HE4), carcinoembryonic antigen (CEA), human chorionicgonadotropin (β-HCG), Bcl-2, Survivin, Bag-1, angiogenin-2 (Ang-2), vascular endothelialgrowth factor (VEGF) and basic fibroblast growth factor (bFGF) levels of observation groupwere significantly lower than those of control group (P0.05) while Bax level was significantlyhigher than that of control group (P0.05). Conclusions: Continuous recombinant humanendostatin pumping combined with TP chemotherapy can decrease the malignant degree ofadvanced ovarian cancer and inhibit angiogenesis.
机译:目的:研究连续重组人内皮抑素联合TP化疗对晚期卵巢癌患者血清恶性分子和血管生成分子的影响。方法:选择2011年7月至2015年12月在我院接受治疗的78例晚期卵巢癌患者,按照单盲随机对照方法分为观察组和对照组(n = 39)。治疗前及治疗4个周期后,用电化学发光免疫分析仪检测血清肿瘤标志物水平。用RIA法测定血清细胞凋亡分子水平。酶联免疫吸附法(ELISA)用于检测血清血管生成分子水平。结果:两组患者治疗前血清肿瘤标志物,凋亡分子和血管生成分子水平差异无统计学意义(P> 0.05)。治疗4个周期后,血清碳水化合物抗原125(CA125),碳水化合物抗原153(CA153),人附睾蛋白4(HE4),癌胚抗原(CEA),人绒毛膜促性腺激素(β-HCG),Bcl-2,Survivin,Bag- 1,观察组的血管生成素2(Ang-2),血管内皮生长因子(VEGF)和碱性成纤维细胞生长因子(bFGF)水平显着低于对照组(P <0.05),而Bax水平显着高于对照组组(P <0.05)。结论:连续重组人内皮抑素联合TP化疗可降低晚期卵巢癌的恶性程度并抑制血管生成。

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