| Literature DB >> 24648925 |
Michael Zebisch1, Alexandra C Kölbl1, Ulrich Andergassen1, Stephan Hutter1, Julia Neugebauer1, Verena Engelstädter1, Maria Günthner-Biller1, Udo Jeschke1, Klaus Friese1, Brigitte Rack1.
Abstract
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.Entities:
Keywords: breast cancer; circulating tumour cells; detection; mRNA; quantification; real-time polymerase chain reaction
Year: 2012 PMID: 24648925 PMCID: PMC3956213 DOI: 10.3892/br.2012.45
Source DB: PubMed Journal: Biomed Rep ISSN: 2049-9434