Safety assessment of benzofuroxan derivatives with potential use in antitubercular therapy by toxicological and toxigenomic approaches

• Grant number: 18/12270-6
• Support Opportunities: Scholarships in Brazil - Post-Doctoral
• Start date: October 01, 2018
• End date: March 31, 2021
• Field of knowledge: Biological Sciences - Microbiology - Applied Microbiology
• Principal Investigator: Fernando Rogério Pavan
• Grantee: Isabel Cristiane da Silva
• Host Institution: Faculdade de Ciências Farmacêuticas (FCFAR). Universidade Estadual Paulista (UNESP). Campus de Araraquara. Araraquara , SP, Brazil
• Associated scholarship(s): 18/24783-8 - Molecular toxicology testing of benzofuraxanes, BE.EP.PD

Abstract

Tuberculosis is a contagious disease caused by Mycobacterium tuberculosis, which mainly attacks lungs and other parts of the body like kidneys, eyes and bones. It is a disease of global incidence, infecting one third of the entire world population. With this, tuberculosis is currently responsible for the deaths of 1.7 million people a year; indices greater than those observed for any other infectious disease in the world, overcoming AIDS.The disease has also become gradually more difficult to treat; it is estimated that in 2050, deaths from resistant bacterial infections will be the number one cause of death in the world.During the last 10 years, our group has been working on the study of different strategies for searching new antimicrobials against TB. More than 5.000 compounds from diferent sources were screened in our laboratory and less than 5% displayed promising activity. Among these, we have been able to find a benzofuroxane-derived lead compound showing an excellent activity in vitro and in vivo and also with a possible new mechanism of action. As a leading molecule, it's activity must to be improved. Thus, the present proposal aims to continue the work that has been done in our group, using molecules derived from the class of newly synthesized benzofuroxanes. For this, parameters related to the toxicological safety of such molecules will be investigated. Will be analyzed: the genotoxic and mutagenic potential; cell death profile (apoptosis / necrosis); gene regulation of toxicologically important cellular functions, permeability, transport and measurement of interindividual differences in the absorption of substances.

Scientific publications

(The scientific publications listed on this page originate from the Web of Science or SciELO databases. Their authors have cited FAPESP grant or fellowship project numbers awarded to Principal Investigators or Fellowship Recipients, whether or not they are among the authors. This information is collected automatically and retrieved directly from those bibliometric databases.)

SOLCIA, MARIANA CRISTINA; CAMPOS, DEBORA LEITE; GRECCO, JULIA ARAUJO; PAIVA SILVA, CAIO SANDER; DA SILVA, PATRICIA BENTO; DA SILVA, ISABEL CRISTIANE; BALDUINO DA SILVA, ANA PAULA; SILVA, JOAS; ODA, FERNANDO BOMBARDA; DOS SANTOS, ANDRE GONZAGA; et al. rowth-inhibitory effects of tris-(1,10-phenanthroline) iron (II) against Mycobacterium tuberculosis in vitro and in viv. TUBERCULOSIS, v. 128, MAY 2021. (20/13497-4, 18/12270-6, 17/12419-7, 16/24633-0, 18/21778-3, 18/12135-1, 18/00163-0)

SOLCIA, MARIANA CRISTINA; CAMPOS, DEBORA LEITE; GRECCO, JULIA ARAUJO; PAIVA SILVA, CAIO SANDER; DA SILVA, PATRICIA BENTO; DA SILVA, ISABEL CRISTIANE; BALDUINO DA SILVA, ANA PAULA; SILVA, JOAS; ODA, FERNANDO BOMBARDA; DOS SANTOS, ANDRE GONZAGA; et al. Growth-inhibitory effects of tris-(1,10-phenanthroline) iron (II) against Mycobacterium tuberculosis in vitro and in vivo. TUBERCULOSIS, v. 128, p. 8-pg., 2021-05-19. (18/00163-0, 16/24633-0, 18/21778-3, 17/12419-7, 18/12270-6, 18/12135-1, 20/13497-4)