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检测转移性头颈部鳞状细胞癌的分子检测法

Molecular assay to detect metastatic head and neck squamous cell carcinoma.

作者信息

Becker Marta T, Shores Carol G, Yu Kathy K, Yarbrough Wendell G

机构信息

Department of Otolaryngology/Head and Surgery, University of North Carolina at Chapel Hill, USA.

出版信息

Arch Otolaryngol Head Neck Surg. 2004 Jan;130(1):21-7. doi: 10.1001/archotol.130.1.21.

Abstract

BACKGROUND

The presence or absence of metastatic disease in cervical lymph nodes is the single most important determinant of therapy and prognosis for patients with head and neck squamous cell carcinoma (HNSCC). However, histologic examination fails to detect metastatic disease in a subset of neck dissection specimens. The accuracy of neck staging may be improved by the use of molecular techniques. Cytokeratins 5, 14, and 20 may be appropriate markers for HNSCC because they are expressed in HNSCC but not in lymphatic tissue.

DESIGN

To test the sensitivity of detection of cytokeratin 5, 14, and 20 messenger RNA by quantitative reverse transcription polymerase chain reaction (RT-PCR), full-length coding DNA sequences were cloned and transcribed. The expression of cytokeratin 5, 14, and 20 messenger RNA was quantified in 4 HNSCC cell lines and 11 tumors. A cell culture lymph node model was created.

RESULTS

As few as 32 molecules of cytokeratin 14 could be detected using quantitative RT-PCR. Cytokeratins 5 and 14 were easily detected in all 4 HNSCC cell lines and almost all tumors. Cytokeratin 20 was not a useful marker, as expression was absent or significantly reduced in cell lines and tumors. In the lymph node model, cytokeratin 14 quantitative RT-PCR was able to detect 1 cancer cell in a background of 10 million lymphatic cells.

CONCLUSIONS

Quantitative RT-PCR detection of cytokeratin 5 or 14 is a sensitive new molecular technique that may be used for detection of cervical micrometastases in head and neck cancer.

摘要

背景

颈部淋巴结转移疾病的存在与否是头颈部鳞状细胞癌(HNSCC)患者治疗和预后的唯一最重要决定因素。然而,组织学检查未能在一部分颈部清扫标本中检测到转移疾病。使用分子技术可能会提高颈部分期的准确性。细胞角蛋白5、14和20可能是HNSCC的合适标志物,因为它们在HNSCC中表达,但在淋巴组织中不表达。

设计

为了通过定量逆转录聚合酶链反应(RT-PCR)测试细胞角蛋白5、14和20信使核糖核酸检测的敏感性,克隆并转录了全长编码DNA序列。在4种HNSCC细胞系和11个肿瘤中对细胞角蛋白5、14和20信使核糖核酸的表达进行了定量。建立了细胞培养淋巴结模型。

结果

使用定量RT-PCR可检测到低至32个细胞角蛋白14分子。在所有4种HNSCC细胞系和几乎所有肿瘤中都很容易检测到细胞角蛋白5和14。细胞角蛋白20不是一个有用的标志物,因为在细胞系和肿瘤中其表达缺失或显著降低。在淋巴结模型中,细胞角蛋白14定量RT-PCR能够在1000万个淋巴细胞的背景中检测到1个癌细胞。

结论

细胞角蛋白5或14的定量RT-PCR检测是一种敏感的新分子技术,可用于检测头颈部癌中的颈部微转移。

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