Serum-free culture success of glial tumors is related to specific molecular profiles and expression of extracellular matrixassociated gene modules

被引:51
作者
Balvers, Rutger K. [1 ]
Kleijn, Anne [1 ]
Kloezeman, Jenneke J. [1 ]
French, Pim J. [2 ]
Kremer, Andreas [3 ]
van den Bent, Martin J. [2 ]
Dirven, Clemens M. F. [1 ]
Leenstra, Sieger [1 ,4 ]
Lamfers, Martine L. M. [1 ]
机构
[1] Erasmus MC, Dept Neurosurg, Brain Tumor Ctr, Rotterdam, Netherlands
[2] Erasmus MC Cancer Inst, Dept Neurol Neurooncol, Brain Tumor Ctr, Rotterdam Mc, Netherlands
[3] Erasmus MC, Erasmus Ctr Bioinformat, Rotterdam Mc, Netherlands
[4] St Elizabeth Hosp, Dept Neurosurg, Tilburg, Netherlands
关键词
extracellular matrix; glioma; IDH1; molecular subtype; serum-free cultures; CANCER STEM-CELLS; OLIGODENDROGLIAL BRAIN-TUMORS; HUMAN GLIOBLASTOMA; NEUROSPHERE FORMATION; MALIGNANT GLIOMA; SURVIVAL; LINES; SUBTYPES; GROWTH; MULTIFORME;
D O I
10.1093/neuonc/not116
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent molecular characterization studies have identified clinically relevant molecular subtypes to coexist within the same histological entities of glioma. Comparative studies between serum-supplemented and serum-free (SF) culture conditions have demonstrated that SF conditions select for glioma stem-like cells, which superiorly conserve genomic alterations. However, neither the representation of molecular subtypes within SF culture assays nor the molecular distinctions between successful and nonsuccessful attempts have been elucidated. A cohort of 261 glioma samples from varying histological grades was documented for SF culture success and clinical outcome. Gene expression and single nucleotide polymorphism arrays were interrogated on a panel of tumors for comparative analysis of SF (successful cultures) and SF (unsuccessful cultures). SF culture outcome was correlated with tumor grade, while no relation was found between SF and patient overall survival. Copy numberbased hierarchical clustering revealed an absolute separation between SF and SF parental tumors. All SF cultures are derived from tumors that are isocitrate dehydrogenase 1 (IDH1) wild type, chromosome 7 amplified, and chromosome 10q deleted. SF cultures derived from IDH1 mutant tumors demonstrated a fade-out of mutated cells during the first passages. SF tumors were enriched for The Cancer Genome Atlas Classical subtype and intrinsic glioma subtype-18. Comparative gene ontology analysis between SF and SF tumors demonstrated enrichment for modules associated with extracellular matrix composition, Hox-gene signaling, and inflammation. SF cultures are derived from a subset of parental tumors with a shared molecular background including enrichment for extracellular matrixassociated gene modules. These results provide leads to develop enhanced culture protocols for glioma samples not propagatable under current SF conditions.
引用
收藏
页码:1684 / 1695
页数:12
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