TY - JOUR
T1 - Potential drug targets in the pentose phosphate pathway of trypanosomatids
AU - Loureiro, Ines
AU - Faria, Joana
AU - Santarem, Nuno
AU - Smith, Terry K.
AU - Tavares, Joana
AU - Cordeiro-da-Silva, Anabela
PY - 2018/11/30
Y1 - 2018/11/30
N2 - The trypanosomatids, Trypanosoma brucei, Trypanosoma cruzi and Leishmania spp, are causative agents of important human diseases such as African sleeping sickness, Chagas' disease and Leishmaniasis, respectively. The high impact of these diseases on human health and economy worldwide, the unsatisfactory available chemotherapeutic options and the absence of human effective vaccines, strongly justifies the search for new drugs. The pentose phosphate pathway has been proposed to be a viable strategy to defeat several infectious diseases, including those from trypanosomatids, as it includes an oxidative branch, important in the maintenance of cell redox homeostasis, and a non-oxidative branch in which ribose 5-phosphate and erythrose 4-phosphate, precursors of nucleic acids and aromatic amino acids, are produced. This review provides an overview of the available chemotherapeutic options against these diseases and discusses the potential of genetically validated enzymes from the pentose phosphate pathway of trypanosomatids to be explored as potential drug targets.
AB - The trypanosomatids, Trypanosoma brucei, Trypanosoma cruzi and Leishmania spp, are causative agents of important human diseases such as African sleeping sickness, Chagas' disease and Leishmaniasis, respectively. The high impact of these diseases on human health and economy worldwide, the unsatisfactory available chemotherapeutic options and the absence of human effective vaccines, strongly justifies the search for new drugs. The pentose phosphate pathway has been proposed to be a viable strategy to defeat several infectious diseases, including those from trypanosomatids, as it includes an oxidative branch, important in the maintenance of cell redox homeostasis, and a non-oxidative branch in which ribose 5-phosphate and erythrose 4-phosphate, precursors of nucleic acids and aromatic amino acids, are produced. This review provides an overview of the available chemotherapeutic options against these diseases and discusses the potential of genetically validated enzymes from the pentose phosphate pathway of trypanosomatids to be explored as potential drug targets.
KW - Trypanosomatids
KW - Treatment
KW - Pentose phosphate pathway
KW - Drug targets
U2 - 10.2174/0929867325666171206094752
DO - 10.2174/0929867325666171206094752
M3 - Review article
SN - 0929-8673
VL - 25
SP - 5239
EP - 5265
JO - Current Medicinal Chemistry
JF - Current Medicinal Chemistry
IS - 39
ER -