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1.400038 重庆,第三军医大学西南医院检验科,全军检验医学中心
2.400016 重庆,重庆医科大学公共卫生与管理学院
[府伟灵,E-mail:fwl@tmmu.edu.cnFU Weiling, E-mail:fwl@tmmu.edu.cn
收稿:2017-09-13,
修回:2017-10-12,
纸质出版:2017-12-30
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王贵宇, 张晓莉, 杨翔, 等. 循环肿瘤细胞分型检测在非小细胞肺癌中的应用[J]. 第三军医大学学报, 2017,39(24):2399-2405.
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王贵宇, 张晓莉, 杨翔, 等. 循环肿瘤细胞分型检测在非小细胞肺癌中的应用[J]. 第三军医大学学报, 2017,39(24):2399-2405. DOI: 10.16016/j.1000-5404.201709095.
Guiyu WANG, Xiaoli ZHANG, Xiang YANG, et al. Typing of circulating tumor cells for non-small cell lung cancer[J]. Journal of Third Military Medical University, 2017, 39(24): 2399-2405. DOI: 10.16016/j.1000-5404.201709095.
目的
2
探讨非小细胞肺癌患者外周血中循环肿瘤细胞(circulating tumor cells
CTCs)的数量和型别分布,分析其与临床病理特征之间的关系。
方法
2
采用最新CanPatrol
TM
CTCs分型检测技术,基于滤膜法收集221例非小细胞肺癌患者外周血中的CTCs,通过RNA原位杂交、分支DNA技术对循环肿瘤细胞内的上皮、间质标志物mRNA进行荧光检测,将CTCs分成上皮型、混合型、间质型,分析其与年龄、性别、临床病理分期和是否远处转移的关系。
结果
2
90.05%非小细胞肺癌患者检出CTCs,3个型别里混合型CTCs检出比例最高。总CTCs,上皮型、混合型、间质型CTCs数量与临床分期和远处转移有关(
P
<0.05),与年龄和性别无关(
P
>
0.05)。Logistic回归分析结果显示,间质型CTCs是临床分期和远处转移的危险因素。
结论
2
在外周血循环肿瘤细胞检测中,数量和分型均有重要价值,其中间质型CTCs可能为非小细胞肺癌患者肿瘤分期及远处转移提供重要线索。
Objective
2
To investigate the number and distribution of circulating tumor cells(CTCs) in peripheral blood of non-small cell lung cancer(NSCLC) patients
and analyze their correlation with clinical pathological features.
Methods
2
The CanPatrol
TM
CTCs enrichment technique was used to isolate and classify CTCs from the peripheral blood samples of 221 NSCLC patients. RNA
in situ
hybridization and branched DNA technology were employed to detect the epithelial and mesenchymal markers of CTCs at mRNA level by fluorescence detection. Based on the results
there were 3 phenotypes identified
that is
epithelial CTCs
biophenotypic (epithelial/mesenchymal) CTCs
and mesenchymal CTCs. And the number and type were analyzed for the correlation with sex
age
clinical stage and distant metastasis.
Results
2
CTCs were detected in 90.05% of NSCLC patients
and of the 3 types
the biophenotypic CTCs took the first rank.The numbers of total CTCs
epithelial CTCs
biophenotypic CTCs
and mesenchymal CTCs were associated with clinical stage and distant metastasis(
P
<
0.05)
but were irrelevant with sex and age(
P
>
0.05). Logistic regression analysis showed that mesenchymal type of CTCs was a risk factor for clinical stage and distant metastasis.
Conclusion
2
Both number and phenotype are important in the detection of CTCs. Mesenchymal CTCs may offer valuable insights for tumor staging and metastatic evaluation in the NSCLC patients.
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