Serum levels of Golgi protein 73 before and after TACE in patients with primary liver cancer and its clinical significance
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摘要: 目的 探讨原发性肝癌(PHC)患者行经导管肝动脉化疗栓塞术(TACE)前后血清高尔基体蛋白73(GP73)变化的临床意义,进一步明确GP73对PHC患者TACE治疗疗效评估、预后监测的意义。 方法 选择2015年1月-12月在蚌埠医学院第一附属医院利用酶联免疫吸附测定法(ELISA)分别检测40例PHC患者TACE术前及术后1 d,术后4~6周血清GP73和AFP值;将40例PHC患者根据TACE治疗疗效分为好转组(28例)和恶化组(12例),分析术前和术后第1天,术后4~6周GP73和AFP的变化与TACE治疗疗效及预后的关系。 结果 好转组患者术前、术后1 d,术后4~6周血清GP73浓度分别为(0.390±0.161)IU/ml,(0.385±0.165)IU/ml,(0.187±0.125)IU/ml,术后1 d血清GP73水平较术前无明显变化(P>0.05),术后4~6周血清GP73水平较术前明显降低(P<0.01);恶化组术前、术后1 d,术后4~6周血清GP73浓度分别(0.373±0.134)IU/ml,(0.372±0.130)IU/ml,(0.604±0.121)IU/ml,恶化组患者术后1 d血清GP73水平较术前无明显变化(P>0.05),术后4~6周血清GP73水平较术前明显升高(P<0.01)。AFP<400 ng/ml时,PHC患者术前与术后1 d、术后4~6周AFP均无明显改变(P>0.05),好转组术后4~6周血清GP73水平较术前下降(P<0.05),恶化组术后4~6周血清GP73水平较术前升高(P<0.05)。 结论 GP73可以作为PHC患者TACE术疗效判断的指标,尤其是在AFP较低或AFP阴性时GP73作为疗效的评价比AFP更有优势。Abstract: Objective To explore the clinical significance of serum Golgi protein 73 (GP73) levels before and after transcatheter arterial chemoembolization (TACE) in patients with primary hepatocellular carcinoma (PHC), and discuss the role of GP73 in the curative effect evaluation and prognosis monitoring among the PHC patients undergoing TRAC. Methods The Enzyme-link immunosorbent assay (ELISA) was used to detect the serum levels of GP73 and AFP in 40 cases of HPC before TACE, D1 after TRAC and 4 to 6 weeks after TACE. Based on the result of TRAC, 40 patients were assigned into the improved group(28 cases) and progression group (12 cases). The relationship between the dynamic levels of GP73 and AFP and the curative effect and prognosis of the patients were analyzed. Results In the improved group, the serum GP73 level before TACE, on the first day and in four to six weeks after TACE were (0.390±0.161) IU/ml, (0.385±0.165) IU/ml and (0.187±0.125) IU/ml, respectively. The serum GP73 level on the first day after TRAC were not significantly improved(P>0.05), however, in the four to six weeks after TRAC it decreased significantly as compared with the preoperative levels (P<0.05). In the progression group, the serum GP73 level before TACE, on the first day after TACE and in the four to six weeks after TACE were (0.373±0.134) IU/ml, (0.372±0.130) IU/ml and (0.604±0.121) IU/ml, respectively. The serum GP73 level did not change significantly on the first day after TRAC(P>0.05), however, it elevated significantly in the four to six weeks after TACE (P<0.05). For the HPC patients with AFP level less than 400 ng/ml, the serum GP73 level in the four to six weeks after TACE significantly decreased in the improved group (P<0.05), but significantly increased in the progression group (P<0.05); however, the AFP level did not change significantly before and after TACE (P>0.05). Conclusion The serum GP73 could be taken as an effective indicator in monitoring the therapeutic effect of TACE in patients with PHC. The GP73 has more advantages than AFP in the monitoring the therapeutic effect of TACE while the serum AFP level is less than 400 ng/ml.
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