A quantitative PCR method to detect blood microRNAs associated with tumorigenesis in transgenic mice

被引:10
作者
Fan, Alice C. [2 ,3 ]
Goldrick, Marianna M. [1 ,5 ]
Ho, Jennifer [1 ]
Liang, Yu [4 ]
Bachireddy, Pavan [2 ,3 ]
Felsher, Dean W. [2 ,3 ]
机构
[1] Amb Appl Biosyst Inc, Austin, TX 78744 USA
[2] Stanford Univ, Sch Med, Div Oncol, Dept Med, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Div Oncol, Dept Pathol, Stanford, CA 94305 USA
[4] Appl Biosyst Inc, Div Mol Cell Biol Assay R&D, Foster City, CA 94404 USA
[5] BIOO Sci, Austin, TX 78744 USA
关键词
D O I
10.1186/1476-4598-7-74
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNA (miRNA) dysregulation frequently occurs in cancer. Analysis of whole blood miRNA in tumor models has not been widely reported, but could potentially lead to novel assays for early detection and monitoring of cancer. To determine whether miRNAs associated with malignancy could be detected in the peripheral blood, we used real-time reverse transcriptase-PCR to determine miRNA profiles in whole blood obtained from transgenic mice with c-MYC-induced lymphoma, hepatocellular carcinoma and osteosarcoma. The PCR-based assays used in our studies require only 10 nanograms of total RNA, allowing serial mini-profiles (20 - 30 miRNAs) to be carried out on individual animals over time. Blood miRNAs were measured from mice at different stages of MYC-induced lymphomagenesis and regression. Unsupervised hierarchical clustering of the data identified specific miRNA expression profiles that correlated with tumor type and stage. The miRNAs found to be altered in the blood of mice with tumors frequently reverted to normal levels upon tumor regression. Our results suggest that specific changes in blood miRNA can be detected during tumorigenesis and tumor regression.
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页数:8
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