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Biomarkers of the Toxic Effects of Chemotherapeutic Agents: A Focus on Antimalarials

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Biomarkers in Toxicology

Abstract

Malaria continues to inflict unacceptably high levels of sickness and mortality, as reported in the previous editions of the World Malaria Report. Antimalarial drugs are the most common treatment for this condition. The gastrointestinal tract, the eyes, the central nervous system, and the cardiovascular system are all affected by antimalarial toxicity; this literature aims to provide an overview of recent advances relating to biomarkers of the toxic effects of antimalarial drugs. Gene polymorphism of metabolizing enzymes; predominantly Cytochrome P450 (CYP) and UDP Glucuronosyltransferase (UGT), drug Transporter; (P-glycoprotein and Organic anion Transporter 1B1), Glutathione S-transferases and deficiency of Glucose-6-Phosphate dehydrogenase (G6PD) are seen as biomarkers of antimalarial drug toxicity. Individual differences in drug response are linked to polymorphisms in the genes encoding these markers. Despite multiple studies on the potential of biomarkers in antimalarial medications, further study is needed to better characterize biomarkers for specific adverse effects (AEs) associated with the use of antimalarial drugs.

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Abbreviations

ACTs:

Artemisinin-based combination therapies

AEs:

Adverse effects

AL:

Artemether–Lumefantrine

AS+AQ:

Artesunate + Amodiaquine

AS+MQ:

Artesunate + Mefloquine

AS+SP:

Artesunate + Sulfadoxine–Pyrimethamine

BCRP:

Breast Cancer Resistance Protein

CNS:

Central Nervous System

CTs:

Combination therapies

CYT:

Cytochrome P450

DEAQ:

N-desethylamodiaquine

DHA + PQ:

Dihydroartemisinin–Piperaquine

G6PD:

Glucose -6- Phosphate dehydrogenase

GST:

Glutathione S-transferases

HIV:

Human immunodeficiency virus infection

MDR:

Multidrug transporter

OATP:

Organic anion transporting peptide

OCTs:

Organic cation transporters

PfMDR:

P. falciparun Multidrug Transporter

P-gp:

P-glycoprotein

QNM:

Quinoneimine

SLCO1B1:

Solute carrier organic anion transporter

SP:

Sulfadoxine–Pyrimethamine

UGT:

UDP Glucuronosyltransferase

W.H.O:

World Health Organization

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Correspondence to David Audu .

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Audu, D., Petagine, L., Idowu, O.A., Patel, V.B., Idowu, A.B. (2023). Biomarkers of the Toxic Effects of Chemotherapeutic Agents: A Focus on Antimalarials. In: Patel, V.B., Preedy, V.R., Rajendram, R. (eds) Biomarkers in Toxicology. Biomarkers in Disease: Methods, Discoveries and Applications. Springer, Cham. https://doi.org/10.1007/978-3-030-87225-0_73-2

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  • DOI: https://doi.org/10.1007/978-3-030-87225-0_73-2

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-030-87225-0

  • Online ISBN: 978-3-030-87225-0

  • eBook Packages: Springer Reference Biomedicine and Life SciencesReference Module Biomedical and Life Sciences

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Chapter history

  1. Latest

    Biomarkers of the Toxic Effects of Chemotherapeutic Agents: A Focus on Antimalarials
    Published:
    12 November 2022

    DOI: https://doi.org/10.1007/978-3-030-87225-0_73-2

  2. Original

    Biomarkers of the Toxic Effects of Chemotherapeutic Agents: A Focus on Antimalarials
    Published:
    01 October 2022

    DOI: https://doi.org/10.1007/978-3-030-87225-0_73-1