AI Article Synopsis

  • Liquid biopsy-based biomarkers like microRNAs could enhance patient management for germ cell tumors, but integration into clinical practice faces challenges.
  • Researchers developed a model to identify and validate clinically relevant microRNAs using multiple data sources, including lab experiments and patient samples.
  • The study highlights the importance of controls, sample types, and pre-analytical variables in liquid biopsy studies, ultimately identifying potential microRNAs (miR-885-5p, miR-448, and miR-197-3p) that may better serve as biomarkers than previously thought ones like miR-375.

Article Abstract

Liquid biopsy-based biomarkers, such as microRNAs, represent valuable tools for patient management, but often do not make it to integration in the clinic. We aim to explore issues impeding this transition, in the setting of germ cell tumors, for which novel biomarkers are needed. We describe a model for identifying and validating clinically relevant microRNAs for germ cell tumor patients, using both in vitro, in vivo (mouse model) and patient-derived data. Initial wide screening of candidate microRNAs is performed, followed by targeted profiling of potentially relevant biomarkers. We demonstrate the relevance of appropriate (negative) controls, experimental conditions (proliferation), and issues related to sample origin (serum, plasma, cerebral spinal fluid) and pre-analytical variables (hemolysis, contaminants, temperature), all of which could interfere with liquid biopsy-based studies and their conclusions. Finally, we show the value of our identification model in a specific scenario, contradicting the presumed role of miR-375 as marker of teratoma histology in liquid biopsy setting. Our findings indicate other putative microRNAs (miR-885-5p, miR-448 and miR-197-3p) fulfilling this clinical need. The identification model is informative to identify the best candidate microRNAs to pursue in a clinical setting.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952794PMC
http://dx.doi.org/10.3390/cells8121637DOI Listing

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