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Serum levels of VEGF-C, VEGF-D, and sVEGF-R2 in patients with lung cancer during chemotherapy.

机译:肺癌患者化疗期间的血清VEGF-C,VEGF-D和sVEGF-R2水平。

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The aim of this study was to assess serum levels of vascular endothelial growth factor C and D (VEGF-C, VEGF-D) and soluble VEGF receptor 2 (sVEGFR-2) in patients with lung cancer during chemotherapy. The study included 80 patients (64 men and 16 women; mean age 61.1) diagnosed histologically with lung cancer. Forty-four (55%) had non-small cell lung cancer (NSCLC) and 36 (45%) had small cell lung cancer (SCLC). Squamous cell carcinoma was established in 56% (25 patients) of all patients with NSCLC, adenocarcinoma in 20% (9 patients), and non-small cell lung cancer in 23% (10 patients). The control group consisted of 20 healthy volunteers. Peripheral blood samples were taken before and after four cycles of chemotherapy. VEGF-C, VEGF-D, and sVEGFR-2 levels were assessed by ELISA method. Serum levels of VEGF-C and VEGF-D were significantly higher in both NSCLC and SCLC groups in comparison with controls. VEGF-C concentration decreased after chemotherapy, whereas VEGF-D concentration was at the same level. No correlation was found between VEGF-C and VEGF-D concentrations and the effect of treatment. Patients with lung cancer and progression after chemotherapy (PD) had the higher concentration of sVEGFR-2 than patients with partial remission (PR). The levels of sVEGFR-2 were lower before and after treatment than in controls. No relation was found between VEGF-C, VEGF-D, and sVEGFR-2 concentrations and the histological type and staging of lung cancer. Summing up, serum concentrations of VEGF-C and VEGF-D were higher in patients with lung cancer both before and after chemotherapy than in healthy controls, whereas sVEGFR-2 concentration was lower than in healthy controls. An increase in concentration of sVEGFR-2 during chemotherapy may suggest progression of the disease. However, it requires further examination.
机译:这项研究的目的是评估化疗期间肺癌患者的血管内皮生长因子C和D(VEGF-C,VEGF-D)和可溶性VEGF受体2(sVEGFR-2)的血清水平。该研究包括组织学诊断为肺癌的80例患者(64例男性和16例女性;平均年龄61.1)。四十四(55%)人患有非小细胞肺癌(NSCLC),三十六(45%)人患有小细胞肺癌(SCLC)。在所有NSCLC患者中,有56%(25名患者)建立了鳞状细胞癌,在20%(9名患者)中建立了腺癌,在23%(10名患者)中建立了非小细胞肺癌。对照组由20名健康志愿者组成。在化疗的四个周期之前和之后采集外周血样品。通过ELISA方法评估VEGF-C,VEGF-D和sVEGFR-2水平。与对照组相比,NSCLC和SCLC组的血清VEGF-C和VEGF-D的水平明显更高。化疗后VEGF-C浓度降低,而VEGF-D浓度处于相同水平。在VEGF-C和VEGF-D浓度与治疗效果之间未发现相关性。肺癌和化疗后进展(PD)患者的sVEGFR-2浓度高于部分缓解(PR)患者。治疗前后sVEGFR-2水平低于对照组。 VEGF-C,VEGF-D和sVEGFR-2的浓度与肺癌的组织学类型和分期之间没有关系。综上所述,肺癌患者化疗前后的血清VEGF-C和VEGF-D的浓度均高于健康对照组,而sVEGFR-2的浓度则低于健康对照组。化疗期间sVEGFR-2的浓度升高可能提示疾病进展。但是,它需要进一步检查。

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