Inokuchi M, Ninomiya I, Tsugawa K, Terada I, Miwa K
Department of Gastroenterologic Surgery, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa 920-8641, Japan.
Br J Cancer. 2003 Nov 3;89(9):1750-6. doi: 10.1038/sj.bjc.6601248.
We have established a highly sensitive and quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) method to detect axillary lymph node metastases of breast cancer. Amplifying cytokeratin 19 (CK19) mRNA transcripts using real-time TaqMan PCR made it possible to quantify axillary metastatic burden. Metastases in 358 axillary lymph nodes obtained from 23 breast cancers of 22 patients were investigated by conventional haematoxylin and eosin (H&E) staining, immunohistochemical staining and quantitative RT-PCR assay. The detection rates of axillary lymph node metastasis using H&E staining, immunohistochemistry and RT-PCR assay were 4.5, 5.9 and 13.1%, respectively. RT-PCR assay was the most sensitive of these three methods for detecting lymph node metastases. Cytokeratin 19 mRNA expression values of both histologically and immunohistochemically positive lymph nodes were significantly higher than the values for lymph nodes judged to be negative by both histological and immunohistochemical methods (P<0.0001), and those of histologically negative, but immunohistochemically positive lymph nodes were significantly higher than the values for lymph nodes judged to be negative by both histological and immunohistochemical methods (P<0.0001). Furthermore, metastatic rates of sentinel nodes were higher than the rates of nonsentinel lymph nodes as measured by all three methods. These results indicate that quantitative RT-PCR assay is a sensitive and reliable method for detecting lymph node metastasis. Furthermore, quantification of metastases in sentinel lymph nodes by quantitative RT-PCR assay may be useful to assess the entire axillary burden of breast cancer patients.
我们建立了一种高灵敏度定量逆转录聚合酶链反应(RT-PCR)方法,用于检测乳腺癌腋窝淋巴结转移。使用实时TaqMan PCR扩增细胞角蛋白19(CK19)mRNA转录本,使得量化腋窝转移负荷成为可能。通过常规苏木精和伊红(H&E)染色、免疫组织化学染色和定量RT-PCR检测,对22例患者的23例乳腺癌所获取的358枚腋窝淋巴结中的转移情况进行了研究。H&E染色、免疫组织化学和RT-PCR检测腋窝淋巴结转移的检出率分别为4.5%、5.9%和13.1%。RT-PCR检测是这三种检测淋巴结转移方法中最灵敏的。组织学和免疫组织化学均呈阳性的淋巴结中细胞角蛋白19 mRNA表达值显著高于组织学和免疫组织化学均判定为阴性的淋巴结(P<0.0001),组织学阴性但免疫组织化学阳性的淋巴结中细胞角蛋白19 mRNA表达值也显著高于组织学和免疫组织化学均判定为阴性的淋巴结(P<0.0001)。此外,通过这三种方法测量,前哨淋巴结的转移率均高于非前哨淋巴结。这些结果表明,定量RT-PCR检测是一种检测淋巴结转移的灵敏且可靠的方法。此外,通过定量RT-PCR检测对前哨淋巴结中的转移灶进行量化,可能有助于评估乳腺癌患者的整个腋窝负荷情况。