Effect of short-term storage of blood samples on gene expression in lung cancer patients

肺癌 基因表达 同源盒蛋白纳米 循环肿瘤细胞 癌症 基因 生物 癌症研究 分子生物学 男科 肿瘤科 医学 转移 遗传学 胚胎干细胞 诱导多能干细胞
作者
Eva Obermayr,Nina Koppensteiner,Nicole Heinzl,Eva Schuster,Barbara Holzer,Hannah Fabikan,Christoph Weinlinger,Oliver Illini,Maximilian J. Hochmair,Robert Zeillinger
出处
期刊:Clinical Chemistry and Laboratory Medicine [De Gruyter]
卷期号:61 (2): 294-301 被引量:3
标识
DOI:10.1515/cclm-2022-0738
摘要

Abstract Objectives The stability of gene transcripts associated with the presence of circulating tumor cells (CTCs) has been predominantly studied in cultured cancer cell lines added to blood samples under artificial conditions. In the present study the effect of storage on CTC-related transcripts was assessed in blood samples taken from patients with non-small lung cancer (n=58). Methods The blood samples were split in two equal parts to compare the gene expression with and without storage for 24 h at ambient temperature without preservative added. After enrichment using the microfluidic Parsortix ® technology, the expression levels of selected genes were assessed using quantitative PCR following a gene-specific pre-amplification. The prognostic relevance of each gene in fresh and stored blood samples was evaluated using the R-package Survminer. Results Some genes were either not affected ( TWIST 1, CDH5 , CK19 ) or upregulated upon storage ( NANOG , MET , UCHL1 ) but still associated with poor prognosis. In contrast, ERBB3 , PTHLH , EpCAM , and TERT were no longer associated with the overall survival of the patients. Conclusions The study demonstrates the surprising stability of CTC-related transcripts, which makes overnight shipping of native blood samples possible. Careful verification is required when using model systems – such as normal blood spiked with tumor cells – or other CTC-related markers, as individual transcripts may respond differently to storage.
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