Identification of di-substituted ureas that prevent growth of trypanosomes through inhibition of translation initiation

Author(s)

Machado, Fabricio Castro ^[1] ; Franco, Caio Haddad ^{[2, 1]} ; dos Santos Neto, Jose Vitorino ^[3] ; Dias-Teixeira, Karina Luiza ^[3] ; Moraes, Carolina Borsoi ^{[2, 4]} ; Lopes, Ulisses Gazos ^[3] ; Aktas, Bertal Huseyin ^{[5, 6]} ; Schenkman, Sergio ^[1]

Affiliation

^[1] Univ Fed Sao Paulo, Escola Paulista Med, Dept Microbiol Imunol & Parasitol, BR-04039032 Sao Paulo, SP - Brazil

^[2] Inst Butantan, Sao Paulo, SP - Brazil

^[3] Univ Fed Rio de Janeiro, Inst Biofis Carlos Chagas Filho, Lab Parasitol Mol, Rio De Janeiro, RJ - Brazil

^[4] Univ Sao Paulo, Inst Ciencias Biomed, Dept Microbiol, Sao Paulo, SP - Brazil

^[5] Brigham & Womens Hosp, Dept Med, Hematol Lab Translat Res, 75 Francis St, Boston, MA 02115 - USA

^[6] Harvard Med Sch, 75 Francis St, Boston, MA 02115 - USA

• Document type: Journal article
• Source: SCIENTIFIC REPORTS; v. 8, MAR 20 2018.
• Web of Science Citations: 1

Abstract

Some 1,3-diarylureas and 1-((1,4-trans)-4-aryloxycyclohexyl)-3-arylureas (cHAUs) activate heme-regulated kinase causing protein synthesis inhibition via phosphorylation of the eukaryotic translation initiation factor 2 (eIF2) in mammalian cancer cells. To evaluate if these agents have potential to inhibit trypanosome multiplication by also affecting the phosphorylation of eIF2 alpha subunit (eIF2 alpha), we tested 25 analogs of 1,3-diarylureas and cHAUs against Trypanosoma cruzi, the agent of Chagas disease. One of them (I-17) presented selectivity close to 10-fold against the insect replicative forms and also inhibited the multiplication of T. cruzi inside mammalian cells with an EC50 of 1-3 mu M and a selectivity of 17-fold. I-17 also prevented replication of African trypanosomes (Trypanosoma brucei bloodstream and procyclic forms) at similar doses. It caused changes in the T. cruzi morphology, arrested parasite cell cycle in G1 phase, and promoted phosphorylation of eIF2 alpha with a robust decrease in ribosome association with mRNA. The activity against T. brucei also implicates eIF2 alpha phosphorylation, as replacement of WT-eIF2 alpha with a non-phosphorylatable eIF2 alpha, or knocking down eIF2 protein kinase-3 by RNAi increased resistance to I-17. Therefore, we demonstrate that eIF2 alpha phosphorylation can be engaged to develop trypanosome-static agents in general, and particularly by interfering with activity of eIF2 kinases. (AU)

• FAPESP's process: 14/01577-2 - The role of eIF2 phosphorylation and sirtuins in the multiplication and differentiation of intracellular Trypanosoma cruzi
• Grantee: Fabrício Castro Machado
• Support Opportunities: Scholarships in Brazil - Doctorate