Validation and Selection of New Reference Genes for RT-qPCR Analysis in Pediatric Glioma of Different Grades

Author:

Hernández-Ochoa BeatrizORCID,Fernández-Rosario Fabiola,Castillo-Rodríguez Rosa AngelicaORCID,Marhx-Bracho Alfonso,Cárdenas-Rodríguez NoemíORCID,Martínez-Rosas VíctorORCID,Morales-Luna Laura,González-Valdez Abigail,Calderón-Jaimes Ernesto,Pérez de la Cruz VerónicaORCID,Rivera-Gutiérrez SandraORCID,Meza-Toledo Sergio,Wong-Baeza CarlosORCID,Baeza-Ramírez Isabel,Gómez-Manzo SaúlORCID

Abstract

Gliomas are heterogeneous, solid, and intracranial tumors that originate from glial cells. Malignant cells from the tumor undergo metabolic alterations to obtain the energy required for proliferation and the invasion of the cerebral parenchyma. The alterations in the expression of the genes related to the metabolic pathways can be detected in biopsies of gliomas of different CNS WHO grades. In this study, we evaluated the expression of 16 candidate reference genes in the HMC3 microglia cell line. Then, statistical algorithms such as BestKeeper, the comparative ΔCT method, geNorm, NormFinder, and RefFinder were applied to obtain the genes most suitable to be considered as references for measuring the levels of expression in glioma samples. The results show that PKM and TPI1 are two novel genes suitable for genic expression studies on gliomas. Finally, we analyzed the expression of genes involved in metabolic pathways in clinical samples of brain gliomas of different CNS WHO grades. RT-qPCR analysis showed that in CNS WHO grade 3 and 4 gliomas, the expression levels of HK1, PFKM, GAPDH, G6PD, PGD1, IDH1, FASN, ACACA, and ELOVL2 were higher than those of CNS WHO grade 1 and 2 glioma biopsies. Hence, our results suggest that reference genes from metabolic pathways have different expression profiles depending on the stratification of gliomas and constitute a potential model for studying the development of this type of tumor and the search for molecular targets to treat gliomas.

Funder

E022 Program, National Institute of Pediatrics, Mexico City, Mexico

CONACyT

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

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