Identification of Endogenous Controls for Use in miRNA Quantification in Human Cancer Cell Lines

Cancer Genomics - Proteomics

RUNE ANDREASSEN¹  KARI FURU²  TRINE B. HAUGEN¹  MRINAL K. DAS¹ 

[1] aculty of Health Sciences, Oslo and Akershus University College of Applied Sciences, Oslo, Norwayaculty of Health Sciences, Oslo and Akershus University College of Applied Sciences, Oslo, Norwayaculty of Health Sciences, Oslo and Akershus University College of Applied Sciences, Oslo, Norway;aculty of Health Sciences, Oslo and Akershus University College of Applied Sciences, Oslo, Norwayepartment of Research, Cancer Registry of Norway, Oslo, Norwayaculty of Health Sciences, Oslo and Akershus University College of Applied Sciences, Oslo, Norwayaculty of Health Sciences, Oslo and Akershus University College of Applied Sciences, Oslo, Norwayepartment of Research, Cancer Registry of Norway, Oslo, Norwayepartment of Research, Cancer Registry of Norway, Oslo, Norwayaculty of Health Sciences, Oslo and Akershus University College of Applied Sciences, Oslo, Norwayepartment of Research, Cancer Registry of Norway, Oslo, Norway

关键词: miRNA;    endogenous control;    qPCR;    human cancer cell lines;    quantification of gene expression;   

DOI  :  

来源: Delinasios GJ CO

【 摘 要 】

Background: miRNAs play important roles in multiple biological processes, and deregulation has been linked to several human diseases, including cancer. Studying changes in miRNA expression in cancer development is commonly performed in vitro in human cancer cell lines using quantitative polymerase chain reaction (qPCR), a method requiring the use of a robust reference gene that displays stable expression across all samples. Materials and Methods: Using the NormFinder software, a selection of commonly used endogeneous controls and miRNAs were tested in six human cancer cell lines to identify for the most suitable gene for use as a reference. Results: The frequently used endogenous control U6B small nuclear RNA (RNU6B) was found to be an unsuitable reference for normalization. The most suitable single endogeneous control identified was miR-25-3p, whereas the best combination of two endogeneous controls was miR-25-3p and miR-93-5p. Conclusion: We identified a single and a pair of miRNAs suitable for use as endogenous controls when performing qPCR-based miRNA expression analyses in human cancer cell lines.

【 授权许可】

Unknown