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应用两步反转录 PCR 技术检测非小细胞肺癌中枢神经系统转移中 ALK 基因重排。

Evaluation of ALK gene rearrangement in central nervous system metastases of non-small-cell lung cancer using two-step RT-PCR technique.

机构信息

Department of Pneumonology, Oncology and Allergology, Medical University of Lublin, Jaczewskiego 8, Lublin, 20-954, Poland.

Department of Neurosurgery and Pediatric Neurosurgery, Medical University of Lublin, Lublin, 20-954, Poland.

出版信息

Clin Transl Oncol. 2017 Dec;19(12):1447-1453. doi: 10.1007/s12094-017-1676-4. Epub 2017 May 22.

Abstract

PURPOSE

RT-PCR technique has showed a promising value as pre-screening method for detection of mRNA containing abnormal ALK sequences, but its sensitivity and specificity is still discussable. Previously, we determined the incidence of ALK rearrangement in CNS metastases of NSCLC using IHC and FISH methods.

MATERIALS

We evaluated ALK gene rearrangement using two-step RT-PCR method with EML4-ALK Fusion Gene Detection Kit (Entrogen, USA). The studied group included 145 patients (45 females, 100 males) with CNS metastases of NSCLC and was heterogeneous in terms of histology and smoking status.

RESULTS

21% of CNS metastases of NSCLC (30/145) showed presence of mRNA containing abnormal ALK sequences. FISH and IHC tests confirmed the presence of ALK gene rearrangement and expression of ALK abnormal protein in seven patients with positive result of RT-PCR analysis (4.8% of all patients, 20% of RT-PCR positive patients). RT-PCR method compared to FISH analysis achieved 100% of sensitivity and only 82.7% of specificity. IHC method compared to FISH method indicated 100% of sensitivity and 97.8% of specificity. In comparison to IHC, RT-PCR showed identical sensitivity with high number of false positive results.

CONCLUSION

Utility of RT-PCR technique in screening of ALK abnormalities and in qualification patients for molecularly targeted therapies needs further validation.

摘要

目的

RT-PCR 技术作为检测含有异常 ALK 序列的 mRNA 的初筛方法显示出良好的应用价值,但它的灵敏度和特异性仍存在争议。在此之前,我们使用免疫组化(IHC)和荧光原位杂交(FISH)方法检测 NSCLC 脑转移患者中 ALK 重排的发生率。

材料

我们使用两步 RT-PCR 方法和 EML4-ALK 融合基因检测试剂盒(Entrogen,美国)来评估 ALK 基因重排。研究组包括 145 例 NSCLC 脑转移患者(45 例女性,100 例男性),其组织学和吸烟状态具有异质性。

结果

21%的 NSCLC 脑转移患者(30/145)的检测结果显示存在含有异常 ALK 序列的 mRNA。FISH 和 IHC 检测结果证实了 7 例 RT-PCR 分析阳性患者中 ALK 基因重排和异常 ALK 蛋白的表达(20%的 RT-PCR 阳性患者,所有患者的 4.8%)。与 FISH 分析相比,RT-PCR 方法的灵敏度为 100%,特异性仅为 82.7%。与 FISH 方法相比,IHC 方法的灵敏度为 100%,特异性为 97.8%。与 IHC 相比,RT-PCR 虽然具有高假阳性率,但也具有相同的灵敏度。

结论

RT-PCR 技术在 ALK 异常筛选和有针对性治疗的患者资格鉴定方面的应用价值需要进一步验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e7a/5700214/88a84316d675/12094_2017_1676_Fig1_HTML.jpg

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