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晚期非小细胞肺癌患者血清酸性谷胱甘肽-S转移酶的表达及临床意义[J]. 肿瘤防治研究, 2007, 34(05): 336-339. DOI: 10.3971/j.issn.1000-8578.1706
引用本文: 晚期非小细胞肺癌患者血清酸性谷胱甘肽-S转移酶的表达及临床意义[J]. 肿瘤防治研究, 2007, 34(05): 336-339. DOI: 10.3971/j.issn.1000-8578.1706
Expression of the Serum GST-π Level in Patients with Advanced NSCLC and Its Clinical Significance[J]. Cancer Research on Prevention and Treatment, 2007, 34(05): 336-339. DOI: 10.3971/j.issn.1000-8578.1706
Citation: Expression of the Serum GST-π Level in Patients with Advanced NSCLC and Its Clinical Significance[J]. Cancer Research on Prevention and Treatment, 2007, 34(05): 336-339. DOI: 10.3971/j.issn.1000-8578.1706

晚期非小细胞肺癌患者血清酸性谷胱甘肽-S转移酶的表达及临床意义

Expression of the Serum GST-π Level in Patients with Advanced NSCLC and Its Clinical Significance

  • 摘要: 目的 通过测定非小细胞肺癌(Nonsmall cell lung cancer,NSCLC)患者血清中酸性谷胱甘肽-S转移酶(GST-π)的含量,探讨GST-π在临床的应用价值。方法 应用ELISA法检测46例NSCLC,19例肺良性病变者(Benign lung diseases,BLD)及60例健康人血清GST-π含量,对46例NSCLC患者行诺维本加顺铂方案化疗两周期并判断疗效。结果 非小细胞肺癌患者血清中GST-π含量明显高于肺良性病变者(P〈0.05)及健康对照者(P〈0.05)。以正常对照组(X^-±2s,166.14ng/ml)为正常上限,NSCLC患者阳性率为54.34%,明显高于肺良性病变组36.84%(P〈0.05)及正常对照组3.33%,4(P〈0.05)。血清GST-π含量在鳞癌中的阳性表达率为57.14%,腺癌为52.00%,两者间的差别无统计学意义(P〉0.05)。血清GST-π表达与NSCLC组织学类型、分期、性别无关(P〉0.05)。46例接受了以顺铂为基础的化疗的NSCLC中,19例对化疗有效,总有效率41.30%。其中25例GST-π表达阳性的NSCLC患者中5例对含铂方案化疗有效,有效率20%。21例GST-π表达阴性的NSCLC患者中14例对含铂方案化疗有效,有效率66.67%。两组间化疗效果的差别有统计学意义(P〈0.05)。结论 血清GST-π可作为NSCLC的肿瘤标志物,血清GST-π表达与NSCLC组织学类型、分期、性别无关。NSCLC患者血清中GST-π的表达阳性者对含铂化疗方案的敏感性低于GST-π的表达阴性者。GST-π的含量是一个有价值的可预测患者对含铂化疗方案的敏感性的指标。

     

    Abstract: Objective  To detect the expression of serum glutathione S-t ransferase-π ( GST-π) level in patients with NSCLC, and to investigate it s clinical significance. Methods  GST-π levels in serum of 46 patients with NSCLC, 19 patients with benign lung diseases and 60 health subjects were detected with ELISA. Forty-six NSCLC patients were given 2 cycles of NVB + DDP chemotherapy and clinical response was evaluated. Results  The mean serum GST-π level was significantly higher in patient s with NSCLC than in those with benign lung disease and health subject s ( P < 0. 05) . Twenty-five of 46 patients with NSCLC (54. 34 %) showed elevated serum GST-π levels above a cutoff value of 166. 14 ng/ml (mean +two standard deviations in 60 healthy control subjects) . The positive rate was significantly higher in patients with NSCLC than in those with benign lung disease 36. 84 % and heavy subjects 3. 33 % ( P <0. 05) . The positive rate of serum GST-π were 57. 14 % in squamous cell carcinoma and 52. 00 % in adenocarcinoma ( P > 0. 05) . No correlation was observed between the GST-πlevel and stage, sex, pathohistology. Of the 46 patient s treated with NVB + DDP chemotherapy, 19 patients responded to chemotherapy (overall response rate, 41. 30 %) . For the 25 patients with positive GST-πexpression, 5 patients responded to chemotherapy, response rate was 20 %. In the 21 patient s with negative GST-πexpression, 14 patients responded to chemotherapy, respone rate was 66. 67 %. This difference was statistically significant ( P < 0. 05) . Conclusion  The serum GST-π level may be a valuable tumor marker for NSCLC, There was no correlation between expression of serum GST-π and stage, sex, pathohistology. The response rate of NSCLC patients with GST-π-negative expression was higher than those with GST-π-positive. GST-2π may be a useful predictor of chemotherapy response.

     

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