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A panel of protein markers for the early detection of lung cancer with bronchial brushing specimens.

一组支气管刷检肺癌早期筛查标本中的蛋白标记物

Liu YZ,Jiang YY,Wang BS,Hao JJ,Shang L,Zhang TT,Cao J,Xu X,Zhan QM,Wang MR

Abstract

To date, no robust biomarkers have been available in clinical practice that can provide an early diagnostic evaluation of lung cancer. The objective of this study was to identify potential biomarkers for the early detection of lung cancer using bronchial brushing specimens.
Immunocytochemistry was used to investigate the expression of 35 proteins in 880 bronchial brushing specimens from both outpatients and inpatients who had either lung cancer or benign lung lesions. An optimal panel was identified that had high sensitivity and considerable specificity for detecting lung cancer. Associations between protein expression and clinicopathologic parameters were assessed.
Tumor protein 53 (TP53), TP63, Ki67, epidermal growth factor receptor (EGFR), minichromosome maintenance complex component 6 (MCM6), MCM7, uncharacterized proteins KIAA1522 and KIAA0317, and ubiquitin-protein ligase UHR1 (ICBP90) frequently presented high expression in bronchial brushing specimens from patients who had lung cancer compared with patients who had benign lung lesions. A 6-protein panel consisting of TP53, Ki67, MCM6, MCM7, KIAA1522, and KIAA0317 was identified as the best combination, with sensitivity of 81.1% (309 of 381 specimens) for detecting nonsmall cell lung cancer (NSCLC) and 86.8% (145 of 167 specimens) for detecting small cell lung cancer (SCLC) (specificity, 83.3%; 65 of 78 specimens). The combination of cytology and the protein panel significantly improved the sensitivity of bronchial brushing examination for detecting lung cancer (P<.00001), which increased from 49.1% to 81% in early stage NSCLC (stage I and II). In combined analyses, the protein panel was positively associated with patient sex (P=.00033), tumor type (P<.00001), tumor location (P<.00001), and lymph node metastasis (P=.028).
The 6-protein panel is a potential biomarker for the early detection of lung cancer in bronchial brushings. Cancer (Cancer Cytopathol) 2014;122:833-841. © 2014 American Cancer Society.

摘要

迄今为止,在临床实践中尚没有用于肺癌早期诊断评估的生物标志物。本文研究目的是为支气管刷检肺癌早期筛查标本寻找潜在生物标记物。
对门诊和住院的肺癌或肺良性病变患者的880例支气管刷检标本进行免疫组化检测,共检测35种蛋白。确定一组对肺癌筛查高度敏感、并认为具有特异性的指标,评估蛋白表达和临床病理特征的相关性。
相比较肺部良性病变患者的支气管刷检样本蛋白表达来说,肿瘤蛋白53(TP53)﹑TP63﹑Ki67﹑表皮生长因子受体(EGFR)﹑微小染色体维持组合蛋白6(MCM6)﹑MCM7﹑非特征性蛋白KIAA1522和KIAA0317﹑泛素蛋白链接酶UHR1(ICBP90)在肺癌患者的支气管刷检样本中常出现高表达。其中,包含TP53﹑Ki67﹑MCM6﹑MCM7﹑KIAA1522和KIAA0317六种蛋白的组合是最佳组合,其检测非小细胞肺癌(NACLC)的敏感性是81.1%(309/381);检测小细胞肺癌的敏感性是86.8%(145/167),特异性是83.3%(65/78)。细胞学和蛋白组合检测可显着提高支气管刷检样本检测肺癌的敏感性(P<.00001),可将早期NSCLC(分期I和II)的检出率从49.1%提高到81%。在综合分析中,蛋白组合表达的阳性率和患者性别(P=.00033)﹑肿瘤类型(P<.00001)﹑肿瘤位置(P<.00001)及淋巴结转移(P=.028)相关。
肺癌支气管刷检样本的早期检测中,这6种蛋白组合是潜在的生物标志物。

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