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基于聚合酶链反应的横纹肌肉瘤诊断:胎儿型乙酰胆碱受体亚基与肌细胞生成素的比较

Polymerase chain reaction-based diagnosis of rhabdomyosarcomas: comparison of fetal type acetylcholine receptor subunits and myogenin.

作者信息

Gattenlöhner S, Müller-Hermelink H K, Marx A

机构信息

Institute of Pathology, University of Wuerzburg, Germany.

出版信息

Diagn Mol Pathol. 1998 Jun;7(3):129-34. doi: 10.1097/00019606-199806000-00001.

Abstract

The diagnosis of rhabdomyosarcoma (RMS) is usually straight-forward when light microscopy and immunohistochemistry are used. However, tumors that exhibit a low degree of differentiation and small biopsies can lead to confusion. In such patients and for the detection of minimal (residual) disease, a polymerase chain reaction (PCR)-based approach would be a valuable diagnostic adjunct. This type of approach would be highly sensitive and should be free from the risk for contamination of the tumor sample with normal tissue. Because myogenin and the alpha and gamma subunit of the fetal type acetylcholine receptor (AChR) are specific immunohistochemical markers for RMS, their expression on the mRNA level in RMS, other childhood and adult tumors, and normal tissues was studied. Although the sensitivity of both approaches was 100% in embryonal and alveolar RMS, detection of myogenin mRNA was not specific for RMS but occurred in normal muscle and the majority of the other normal tissues and childhood tumors. Conversely, detection of fetal AChR mRNA as defined by an alpha/tau ratio of < 1 was encountered only in RMS and denervated muscle. The authors conclude that mRNA of the fetal type AChR but not myogenin is a highly specific and sensitive target for the PCR-based diagnosis of RMS.

摘要

当采用光学显微镜检查和免疫组织化学方法时,横纹肌肉瘤(RMS)的诊断通常很直接。然而,分化程度低的肿瘤和小活检标本可能会导致诊断混淆。对于此类患者以及检测微小(残留)疾病,基于聚合酶链反应(PCR)的方法将是一种有价值的诊断辅助手段。这种方法灵敏度很高,且应不存在肿瘤样本被正常组织污染的风险。由于生肌调节因子以及胎儿型乙酰胆碱受体(AChR)的α和γ亚基是RMS的特异性免疫组织化学标志物,因此研究了它们在RMS、其他儿童和成人体肿瘤以及正常组织中的mRNA水平表达。尽管在胚胎型和肺泡型RMS中两种方法的灵敏度均为100%,但生肌调节因子mRNA的检测并非RMS所特有,在正常肌肉以及大多数其他正常组织和儿童肿瘤中也会出现。相反,仅在RMS和失神经肌肉中检测到α/τ比率<1所定义的胎儿型AChR mRNA。作者得出结论,胎儿型AChR的mRNA而非生肌调节因子是基于PCR诊断RMS的高度特异性和敏感的靶点。

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