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Parasitologists United Journal
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Volume Volume 18 (2025)
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Volume Volume 15 (2022)
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Abaza, S. (2022). Recent advances in identification of potential drug targets and development of novel drugs in parasitic diseases. Part IV. Plasmodium spp.. Parasitologists United Journal, 15(3), 238-255. doi: 10.21608/puj.2022.171955.1192
Sherif Abaza. "Recent advances in identification of potential drug targets and development of novel drugs in parasitic diseases. Part IV. Plasmodium spp.". Parasitologists United Journal, 15, 3, 2022, 238-255. doi: 10.21608/puj.2022.171955.1192
Abaza, S. (2022). 'Recent advances in identification of potential drug targets and development of novel drugs in parasitic diseases. Part IV. Plasmodium spp.', Parasitologists United Journal, 15(3), pp. 238-255. doi: 10.21608/puj.2022.171955.1192
Abaza, S. Recent advances in identification of potential drug targets and development of novel drugs in parasitic diseases. Part IV. Plasmodium spp.. Parasitologists United Journal, 2022; 15(3): 238-255. doi: 10.21608/puj.2022.171955.1192

Recent advances in identification of potential drug targets and development of novel drugs in parasitic diseases. Part IV. Plasmodium spp.

Article 4, Volume 15, Issue 3, December 2022, Page 238-255  XML PDF (572.85 K)
Document Type: Review Article
DOI: 10.21608/puj.2022.171955.1192
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Author
Sherif Abaza email
Medical Parasitology Department, Faculty of Medicine, Suez Canal University, Ismailia, Egypt
Abstract
In the last two decades, transporters attracted much attention in identification of potential drug targets
against intracellular protozoa. Several membrane molecules exhibit essential roles in trafficking pathways
for nutrients, essential enzymes and virulence factors. In this context, P. falciparum possesses a complex
of genomic plasticity-encoding transporters with high potentiality for aneuploidy, and gene expression
modulation in response to drug exposure. Therefore, it is able to undergo gene mutations in enzymes controlling
drug uptake, and evade host immune response by antigenic variations as well. The genetic mechanism of
antimalarial drug resistance arises early with monotherapy using fast-acting drugs or a single targeting drug.
Accordingly, combined therapy acting on multiple targets would decrease the emergence of drug resistance.
Evolutionary technology on genetic approach enabled researchers to identify and propose novel Plasmodium
drug targets. The main objective of this part is to review potential drug targets for apicomplexans and discuss
recent approaches in identifying Plasmodium targets, as well as advances in the design and development of
novel antimalarial drugs.
Keywords
apicoplast; drug targets; egress; intracellular protozoa; mitochondria; novel drugs; Plasmodium spp
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