首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Detection of occult tumor cells in lymph nodes from non-small cell lung cancer patients using reverse transcription-polymerase chain reaction for carcinoembryonic antigen mRNA with the evaluation of its sensitivity.
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Detection of occult tumor cells in lymph nodes from non-small cell lung cancer patients using reverse transcription-polymerase chain reaction for carcinoembryonic antigen mRNA with the evaluation of its sensitivity.

机译:应用逆转录聚合酶链反应检测癌胚抗原mRNA,检测非小细胞肺癌患者淋巴结中隐匿性肿瘤细胞,并对其敏感性进行评估。

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摘要

We evaluated the usefulness of a real-time quantitative reverse transcription-polymerase chain reaction (RT-PCR) method for detecting occult tumor cells in histologically malignant-negative lymph nodes resected from patients with non-small cell lung cancer. First, we examined the relationship between tumor cell number and carcinoembryonic antigen (CEA) mRNA copy number using a PCR method with a cancer cell line (A549) in a serial dilution study. Next, we evaluated the relationship between nodal metastatic area size and CEA mRNA copy number using lymph nodes with histologically proven metastasis in a serial slice study. On the basis of those results, we performed RT-PCR analyses with 28 primary tumors and 211 lymph nodes from 28 patients who underwent a lobectomy with systematic node dissection. Our results in the serial dilution study showed that the detectable limitation by quantitative RT-PCR was 25-100 neoplastic cells and 20-100 CEA mRNA copy numbers. In the serial slice study, we found a correlation between CEA mRNA copy number and nodal metastatic area. In the clinical samples, amplification of CEA mRNA was obtained with all 28 primary tumors and 13 of the lymph nodes with metastasis shown by hematoxylin-eosin staining. Furthermore, 52 (25%) of 211 histologically negative lymph nodes and the specimens from 14 (64%) of the 22 pN0 patients revealed a significant level of CEA mRNA. These results indicate that micrometastases, which are not detectable with conventional examinations, can be detected by the present method of RT-PCR for CEA mRNA in a proportion of patients with resected pN0 non-small cell lung cancer.
机译:我们评估了实时定量逆转录聚合酶链反应(RT-PCR)方法在从非小细胞肺癌患者切除的组织学恶性阴性淋巴结中检测隐匿性肿瘤细胞的有用性。首先,在系列稀释研究中,我们使用带有癌细胞系(A549)的PCR方法检查了肿瘤细胞数量与癌胚抗原(CEA)mRNA复制数量之间的关系。接下来,我们在系列切片研究中使用经组织学证实为转移的淋巴结评估了淋巴结转移区域大小与CEA mRNA拷贝数之间的关系。在这些结果的基础上,我们对28例行系统性淋巴结清扫的患者的28例原发肿瘤和211淋巴结进行了RT-PCR分析。我们在系列稀释研究中的结果表明,定量RT-PCR的可检测限为25-100个肿瘤细胞和20-100个CEA mRNA拷贝数。在连续切片研究中,我们发现CEA mRNA拷贝数与淋巴结转移区域之间存在相关性。在临床样品中,苏木精-曙红染色显示,所有28例原发肿瘤和13例有转移的淋巴结均获得CEA mRNA扩增。此外,在211例组织学阴性的淋巴结中,有52例(25%)和22例pN0患者中的14例(64%)的标本显示出显着水平的CEA mRNA。这些结果表明,通过本发明的RT-PCR对CEA mRNA的本发明RT-PCR方法可以在一部分切除的pN0非小细胞肺癌患者中检测到微转移,这是常规检查无法检测到的。

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