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通过多种mRNA标志物检测乳腺癌患者前哨淋巴结中的转移灶。

Detection of metastases in sentinel lymph nodes of breast cancer patients by multiple mRNA markers.

作者信息

Weigelt B, Verduijn P, Bosma A J, Rutgers E J, Peterse H L, van't Veer L J

机构信息

Division of Experimental Therapy, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.

出版信息

Br J Cancer. 2004 Apr 19;90(8):1531-7. doi: 10.1038/sj.bjc.6601659.

Abstract

Disseminated breast tumour cells in sentinel lymph nodes (SNs) were evaluated by quantitative real-time PCR and the sensitivity of this assay was compared to the routine histological analysis. First, several candidate marker genes were tested for their specificity in axillary lymph nodes (ALN) of 50 breast cancer patients and 43 women without breast cancer. The marker gene panel selected, designed to detect the mRNA of CK19, p1B, EGP2 and SBEM, was subsequently applied to detect metastases in 70 SNs that were free of metastases as determined by standard histological evaluation. Remarkably, seven negative SNs showed increased marker gene expression, suggesting the presence of (micro) metastases. Four of these seven SNs positive by real-time PCR proved to contain tumour deposits after careful review of the slides or further sectioning of the paraffin-embedded material. In three PCR positive SNs, however, no tumour cells were found by haematoxylin and eosin staining (H&E) and immunohistologically analysis. The quantitative real-time PCR assay with multiple mRNA markers for the detection of disseminated breast cancer cells in SNs thus resulted in an upstaging of SNs containing metastastic disease of 10% compared to the routine histological analysis. The application of this technique may be of clinical relevance, as it is suggested that micrometastatic disease in SNs are associated with further nodal non-SN metastases in breast cancer.

摘要

通过定量实时聚合酶链反应(PCR)评估前哨淋巴结(SNs)中的播散性乳腺肿瘤细胞,并将该检测方法的敏感性与常规组织学分析进行比较。首先,对50例乳腺癌患者和43例无乳腺癌的女性腋窝淋巴结(ALN)中的几种候选标记基因进行特异性检测。随后,将选定的用于检测细胞角蛋白19(CK19)、p1B、上皮糖蛋白2(EGP2)和乳腺丝束蛋白(SBEM)mRNA的标记基因组合应用于检测70个经标准组织学评估确定无转移的SNs中的转移灶。值得注意的是,7个阴性SNs显示标记基因表达增加,提示存在(微)转移。在仔细复查玻片或对石蜡包埋材料进行进一步切片后,这7个经实时PCR检测为阳性的SNs中有4个被证实含有肿瘤沉积物。然而,在3个PCR阳性的SNs中,苏木精-伊红染色(H&E)和免疫组织学分析均未发现肿瘤细胞。因此,与常规组织学分析相比,用于检测SNs中播散性乳腺癌细胞的多种mRNA标记物的定量实时PCR检测使含有转移性疾病的SNs分期上调了10%。该技术的应用可能具有临床意义,因为有研究表明SNs中的微转移疾病与乳腺癌中进一步的非前哨淋巴结转移有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f001/2409726/288889f2a69c/90-6601659f1.jpg

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