Zebisch Michael, Kölbl Alexandra C, Andergassen Ulrich, Hutter Stephan, Neugebauer Julia, Engelstädter Verena, Günthner-Biller Maria, Jeschke Udo, Friese Klaus, Rack Brigitte
Department of Obstetrics and Gynaecology, Ludwig-Maximilians University of Munich, Munich, Germany.
Biomed Rep. 2013 Mar;1(2):231-234. doi: 10.3892/br.2012.45. Epub 2012 Dec 5.
Circulating tumour cells were detected and quantified by real-time polymerase chain reaction (PCR) in peripheral blood, based on the fact that the expression of certain genes is upregulated in tumour tissues in comparison to surrounding blood cells. Calibration curves showing gene expression as functions of the number of tumour cells within a blood sample were prepared. Blood samples were therefore spiked with cells of breast cancer cell lines, RNA was extracted, transcribed to complementary DNA (cDNA) and used in real-time PCR reaction on the Cytokeratins (CK) 8, 18 and 19. Calibration curves were generated by Microsoft™ Excel®. Relative quantification curves of gene expression in different breast cancer cell lines showed no unitary tendencies. The oscillations in the relative quantification curves of gene expression suggested an occurrence of immunological effects, leading to an apparent agglutination of added tumour cells together with the blood cells of the sample. Thus, strategies to obtain evaluable results should be considered.
基于某些基因在肿瘤组织中相对于周围血细胞表达上调这一事实,通过实时聚合酶链反应(PCR)在外周血中检测和定量循环肿瘤细胞。制备了显示基因表达与血样中肿瘤细胞数量关系的校准曲线。因此,向血样中加入乳腺癌细胞系的细胞,提取RNA,转录为互补DNA(cDNA),并用于细胞角蛋白(CK)8、18和19的实时PCR反应。校准曲线由Microsoft™ Excel®生成。不同乳腺癌细胞系中基因表达的相对定量曲线没有单一趋势。基因表达相对定量曲线的波动表明存在免疫效应,导致添加的肿瘤细胞与样品中的血细胞明显凝集。因此,应考虑获得可评估结果的策略。