TY - JOUR
T1 - Identification and Validation Model for Informative Liquid Biopsy-Based microRNA Biomarkers
T2 - Insights from Germ Cell Tumor In Vitro, In Vivo and Patient-Derived Data
AU - Lobo, João
AU - Gillis, Ad J M
AU - van den Berg, Annette
AU - Dorssers, Lambert C J
AU - Belge, Gafanzer
AU - Dieckmann, Klaus-Peter
AU - Roest, Henk P
AU - van der Laan, Luc J W
AU - Gietema, Jourik
AU - Hamilton, Robert J
AU - Jerónimo, Carmen
AU - Henrique, Rui
AU - Salvatori, Daniela
AU - Looijenga, Leendert H J
PY - 2019/12/14
Y1 - 2019/12/14
N2 - 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.
AB - 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.
KW - Adult
KW - Animals
KW - Biomarkers, Tumor/blood
KW - Cell Line, Tumor
KW - Disease Models, Animal
KW - Female
KW - Humans
KW - Liquid Biopsy/methods
KW - Male
KW - Mice
KW - Mice, Nude
KW - MicroRNAs/analysis
KW - Middle Aged
KW - Neoplasms, Germ Cell and Embryonal/genetics
KW - Xenograft Model Antitumor Assays
U2 - 10.3390/cells8121637
DO - 10.3390/cells8121637
M3 - Article
C2 - 31847394
SN - 2073-4409
VL - 8
JO - Cells
JF - Cells
IS - 12
M1 - 1637
ER -