Cerebrospinal Fluid Biomarkers in Childhood Leukemias

Involvement of the central nervous system (CNS) in childhood leukemias remains a major cause of treatment failures. Analysis of the cerebrospinal fluid constitutes the most important diagnostic pillar in the detection of CNS leukemia and relies primarily on cytological and flow-cytometry studies. Wi...

Full description

Bibliographic Details
Main Author: Chrysanthy Ikonomidou
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/13/3/438
id doaj-908c9422a49b4c7db49a0fc4ea9c16f9
record_format Article
spelling doaj-908c9422a49b4c7db49a0fc4ea9c16f92021-01-25T00:01:37ZengMDPI AGCancers2072-66942021-01-011343843810.3390/cancers13030438Cerebrospinal Fluid Biomarkers in Childhood LeukemiasChrysanthy Ikonomidou0Department of Neurology, University of Wisconsin Madison, 1685 Highland Avenue, Madison, WI 53705, USAInvolvement of the central nervous system (CNS) in childhood leukemias remains a major cause of treatment failures. Analysis of the cerebrospinal fluid constitutes the most important diagnostic pillar in the detection of CNS leukemia and relies primarily on cytological and flow-cytometry studies. With increasing survival rates, it has become clear that treatments for pediatric leukemias pose a toll on the developing brain, as they may cause acute toxicities and persistent neurocognitive deficits. Preclinical research has demonstrated that established and newer therapies can injure and even destroy neuronal and glial cells in the brain. Both passive and active cell death forms can result from DNA damage, oxidative stress, cytokine release, and acceleration of cell aging. In addition, chemotherapy agents may impair neurogenesis as well as the function, formation, and plasticity of synapses. Clinical studies show that neurocognitive toxicity of chemotherapy is greatest in younger children. This raises concerns that, in addition to injury, chemotherapy may also disrupt crucial developmental events resulting in impairment of the formation and efficiency of neuronal networks. This review presents an overview of studies demonstrating that cerebrospinal fluid biomarkers can be utilized in tracing both CNS disease and neurotoxicity of administered treatments in childhood leukemias.https://www.mdpi.com/2072-6694/13/3/438central nervous systemCNS leukemianeurotoxicitysynaptic plasticitycell deathneurocognitive outcome
collection DOAJ
language English
format Article
sources DOAJ
author Chrysanthy Ikonomidou
spellingShingle Chrysanthy Ikonomidou
Cerebrospinal Fluid Biomarkers in Childhood Leukemias
Cancers
central nervous system
CNS leukemia
neurotoxicity
synaptic plasticity
cell death
neurocognitive outcome
author_facet Chrysanthy Ikonomidou
author_sort Chrysanthy Ikonomidou
title Cerebrospinal Fluid Biomarkers in Childhood Leukemias
title_short Cerebrospinal Fluid Biomarkers in Childhood Leukemias
title_full Cerebrospinal Fluid Biomarkers in Childhood Leukemias
title_fullStr Cerebrospinal Fluid Biomarkers in Childhood Leukemias
title_full_unstemmed Cerebrospinal Fluid Biomarkers in Childhood Leukemias
title_sort cerebrospinal fluid biomarkers in childhood leukemias
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2021-01-01
description Involvement of the central nervous system (CNS) in childhood leukemias remains a major cause of treatment failures. Analysis of the cerebrospinal fluid constitutes the most important diagnostic pillar in the detection of CNS leukemia and relies primarily on cytological and flow-cytometry studies. With increasing survival rates, it has become clear that treatments for pediatric leukemias pose a toll on the developing brain, as they may cause acute toxicities and persistent neurocognitive deficits. Preclinical research has demonstrated that established and newer therapies can injure and even destroy neuronal and glial cells in the brain. Both passive and active cell death forms can result from DNA damage, oxidative stress, cytokine release, and acceleration of cell aging. In addition, chemotherapy agents may impair neurogenesis as well as the function, formation, and plasticity of synapses. Clinical studies show that neurocognitive toxicity of chemotherapy is greatest in younger children. This raises concerns that, in addition to injury, chemotherapy may also disrupt crucial developmental events resulting in impairment of the formation and efficiency of neuronal networks. This review presents an overview of studies demonstrating that cerebrospinal fluid biomarkers can be utilized in tracing both CNS disease and neurotoxicity of administered treatments in childhood leukemias.
topic central nervous system
CNS leukemia
neurotoxicity
synaptic plasticity
cell death
neurocognitive outcome
url https://www.mdpi.com/2072-6694/13/3/438
work_keys_str_mv AT chrysanthyikonomidou cerebrospinalfluidbiomarkersinchildhoodleukemias
_version_ 1724324714866802688