Letícia M. R. Pescinelli
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Letícia M. R. Pescinelli has a total of 10 co-authors. Here are the top co-authors by number of shared publications:
- Aislan Cristina Rheder Fagundes Pascoal
Research Laboratory of Natural Products and Bioactive Molecules, (Lab Nat—UFF) Nova Friburgo Health Institute, Fluminense Federal University—UFF, Nova Friburgo 28625-650, RJ, Brazil
1 shared publication - Giovana G. F. V. de Oliveira
Research Laboratory of Natural Products and Bioactive Molecules, (Lab Nat—UFF) Nova Friburgo Health Institute, Fluminense Federal University—UFF, Nova Friburgo 28625-650, RJ, Brazil
1 shared publication - Ivo José Curcino Vieira
Universidade Estadual do Norte Fluminense Darcy Ribeiro (UENF)
1 shared publication - Júlio César Thurler Júnior
Laboratório de Rastreamento Biológico de Novas Drogas Contra o Câncer (CancerBioScreen), Departamento de Ciências Básicas, Instituto de Saúde de Nova Friburgo (ISNF), Universidade Federal Fluminense (UFF), Nova Friburgo CEP 28625-650, RJ, Brazil
1 shared publication - Lucas Silva Abreu
Fluminense Federal University
1 shared publication - Mariana Toledo Martins Pereira
Research Laboratory of Natural Products and Bioactive Molecules, (Lab Nat—UFF) Nova Friburgo Health Institute, Fluminense Federal University—UFF, Nova Friburgo 28625-650, RJ, Brazil
1 shared publication
Latest Publications
- Open Access
- 14 August 2025
- Published by MDPI AG in Pharmaceuticals
- Vol. 18 (8) , 1199
Eugenia uniflora L.: Analysis of Chemical Profile and Cytotoxic Action on Tumor (HeLa) and Non-Tumor Cells (NIH/3T3)
Objectives: This study analyzed the antiproliferative potential of Eugenia uniflora L. leaf extracts against cervical cancer and non-cancerous cell lines. Methods: The extracts were prepared by maceration using hexane (EUH), dichloromethane (EUD), and ethyl acetate (EUA). Their cytotoxic potential was evaluated through MTT assays, wound healing assays, and flow cytometry. To identify classes of secondary metabolites, total phenolic and flavonoid contents were quantified using spectrophotometric methods, and individual metabolites were tentatively identified by LC-MS/MS. Results: EUH, EUD. and EUA exhibited cytotoxicity in HeLa cells, with IC50 values of 63.03 μg/mL, 33.79 μg/mL, and 38.38 μg/mL, respectively. Due to their lower IC50 values, the EUD and EUA fractions were selected for further investigation. EUA and EUD inhibited cell migration at all the time points tested and altered the cell cycle. Twenty-eight compounds were tentatively identified in E. uniflora L. leaf extracts based on the interpretation of their fragmentation patterns and molecular formulas obtained from mass spectrometry. Conclusions: The EUD and EUA extracts appear to modulate the metabolism of cervical cancer cells, leading to cell cycle arrest and inhibition of cell migration. Flavonoids and other phenolic compounds are likely responsible for these observed biological effects.
- 14 August 2025
- Published by MDPI AG in Pharmaceuticals
- Vol. 18 (8) , 1199
Open AccessEugenia uniflora L.: Analysis of Chemical Profile and Cytotoxic Action on Tumor (HeLa) and Non-Tumor Cells (NIH/3T3)
Objectives: This study analyzed the antiproliferative potential of Eugenia uniflora L. leaf extracts against cervical cancer and non-cancerous cell lines. Methods: The extracts were prepared by maceration using hexane (EUH), dichloromethane (EUD), and ethyl acetate (EUA). Their cytotoxic potential was evaluated through MTT assays, wound healing assays, and flow cytometry. To identify classes of secondary metabolites, total phenolic and flavonoid contents were quantified using spectrophotometric methods, and individual metabolites were tentatively identified by LC-MS/MS. Results: EUH, EUD. and EUA exhibited cytotoxicity in HeLa cells, with IC50 values of 63.03 μg/mL, 33.79 μg/mL, and 38.38 μg/mL, respectively. Due to their lower IC50 values, the EUD and EUA fractions were selected for further investigation. EUA and EUD inhibited cell migration at all the time points tested and altered the cell cycle. Twenty-eight compounds were tentatively identified in E. uniflora L. leaf extracts based on the interpretation of their fragmentation patterns and molecular formulas obtained from mass spectrometry. Conclusions: The EUD and EUA extracts appear to modulate the metabolism of cervical cancer cells, leading to cell cycle arrest and inhibition of cell migration. Flavonoids and other phenolic compounds are likely responsible for these observed biological effects.