Novel Molecular Markers in Glioblastoma-Benefits of Liquid Biopsy

Int J Mol Sci. 2020 Oct 12;21(20):7522. doi: 10.3390/ijms21207522.

Abstract

: Glioblastoma is a primary Central Nervous System (CNS) malignancy with poor survival. Treatment options are scarce and despite the extremely heterogeneous nature of the disease, clinicians lack prognostic and predictive markers to characterize patients with different outcomes. Certain immunohistochemistry, FISH, or PCR-based molecular markers, including isocitrate dehydrogenase1/2 (IDH1/2) mutations, epidermal growth factor receptor variant III (EGFRvIII) mutation, vascular endothelial growth factor overexpression (VEGF) overexpression, or (O6-Methylguanine-DNA methyltransferase promoter) MGMT promoter methylation status, are well-described; however, their clinical usefulness and accuracy is limited, and tumor tissue samples are always necessary. Liquid biopsy is a developing field of diagnostics and patient follow up in multiple types of cancer. Fragments of circulating nucleic acids are collected in various forms from different bodily fluids, including serum, urine, or cerebrospinal fluid in order to measure the quality and quantity of these markers. Multiple types of nucleic acids can be analyzed using liquid biopsy. Circulating cell-free DNA, mitochondrial DNA, or the more stable long and small non-coding RNAs, circular RNAs, or microRNAs can be identified and measured by novel PCR and next-generation sequencing-based methods. These markers can be used to detect the previously described alterations in a minimally invasive method. These markers can be used to differentiate patients with poor or better prognosis, or to identify patients who do not respond to therapy. Liquid biopsy can be used to detect recurrent disease, often earlier than using imaging modalities. Liquid biopsy is a rapidly developing field, and similarly to other types of cancer, measuring circulating tumor-derived nucleic acids from biological fluid samples could be the future of differential diagnostics, patient stratification, and follow up in the future in glioblastoma as well.

Keywords: circulating cell-free nucleic acids; glioblastoma; integrated diagnostics; liquid biopsy; prognosis.

Publication types

  • Review

MeSH terms

  • Biomarkers, Tumor*
  • Cell-Free Nucleic Acids
  • Central Nervous System Neoplasms / diagnosis*
  • Central Nervous System Neoplasms / etiology
  • Central Nervous System Neoplasms / metabolism
  • DNA, Neoplasm
  • Disease Susceptibility
  • Extracellular Vesicles
  • Glioblastoma / diagnosis*
  • Glioblastoma / etiology
  • Glioblastoma / metabolism
  • Humans
  • Liquid Biopsy* / methods
  • Liquid Biopsy* / standards
  • Neoplastic Cells, Circulating

Substances

  • Biomarkers, Tumor
  • Cell-Free Nucleic Acids
  • DNA, Neoplasm