Technical Stability and Biological Variability in MicroRNAs from Dried Blood Spots: A Lung Cancer Therapy-Monitoring Showcase.

BACKGROUND: Different work flows have been proposed to use miRNAs as blood-borne biomarkers. In particular, the method used for collecting blood from patients can considerably influence the diagnostic results. METHODS: We explored whether dried blood spots (DBSs) facilitate stable miRNA measurements...

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Publicado en:Clinical Chemistry Vol. 63; no. 9; pp. 1476 - 1489
Autores principales: Kahraman, Mustafa, Laufer, Thomas, Backes, Christina, Schrörs, Hannah, Fehlmann, Tobias, Ludwig, Nicole, Kohlhaas, Jochen, Meese, Eckart, Wehler, Thomas, Bals, Robert, Keller, Andreas
Formato: Journal Article
Publicado: Oxford University Press / USA 2017
Acceso en línea:Ver este registro en EBSCOhost
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      pub: Oxford University Press / USA
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        10.1373/clinchem.2017.271619
        125352821
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        atl: Technical Stability and Biological Variability in MicroRNAs from Dried Blood Spots: A Lung Cancer Therapy-Monitoring Showcase.
      aug:
        au:
          Kahraman, Mustafa
          Laufer, Thomas
          Backes, Christina
          Schrörs, Hannah
          Fehlmann, Tobias
          Ludwig, Nicole
          Kohlhaas, Jochen
          Meese, Eckart
          Wehler, Thomas
          Bals, Robert
          Keller, Andreas
        affil: Clinical Bioinformatics, Saarland University, Homburg, Germany.
      sug:
      ab: BACKGROUND: Different work flows have been proposed to use miRNAs as blood-borne biomarkers. In particular, the method used for collecting blood from patients can considerably influence the diagnostic results. METHODS: We explored whether dried blood spots (DBSs) facilitate stable miRNA measurements and compared its technical stability with biological variability. First, we tested the stability of DBS samples by generating from 1 person 18 whole-genome-wide miRNA profiles of DBS samples that were exposed to different temperature and humidity conditions. Second, we investigated technical reproducibility by performing 7 replicates of DBS again from 1 person. Third, we investigated DBS samples from 53 patients with lung cancer undergoing different therapies. Across these 3 stages, 108 genome-wide miRNA profiles from DBS were generated and evaluated biostatistically. RESULTS: In the stability analysis, we observed that temperature and humidity had an overall limited influence on the miRNomes (average correlation between the different conditions of 0.993). Usage of a silica gel slightly diminished DBS’ technical reproducibility. The 7 technical replicates had an average correlation of 0.996. The correlation with whole-blood PAXGene miRNomes of the same individual was remarkable (correlation of 0.88). Finally, evaluation of the samples from the 53 patients with lung cancer exposed to different therapies showed that the biological variations exceeded the technical variability significantly (P 0.0001), yielding 51 dysregulated miRNAs. CONCLUSIONS: We present a stable work flow for profiling of whole miRNomes on the basis of samples collected from DBS. Biological variations exceeded technical variations significantly. DBS-based miRNA profiles will potentially further the translational character of miRNA biomarker studies.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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