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Background: Eight plant species from Oaxaca, some of them used in traditional medicine, were subjected to screening of several biological activities to provide data regarding their anticancer potential, although no scientific information is available about their pharmacological effects.
Materials And Methods: Methanol extracts from stems or roots of the eight plants were tested for antioxidant activity by the DPPH- method. Antimicrobial activity was determined using the agar diffusion method and the minimal inhibitory concentration (MIC) was obtained by broth dilution method. Antitopoisomerase activity was assessed using mutant strains of JN362a, JN394, JN394t, JN394t. and JN394t. The mutagenic activity was evaluated using the Ames test ( TA1535).
Results: No extract showed significant antioxidant activity. The best antimicrobial activity was observed for (MIC 56.25 μg/mL) and (MIC 78.12 μg/mL) against . Extracts of , and stems showed antitopoisomerase II activity with JN394 growth of -30.88±0.0%, -38.11±4.95%, and -70.97±12.02% respectively. stem extract showed antitopoisomerase I activity with growth of 35.31±6.36% on the same mutant strain. All plant extracts were non-mutagenic. Fractionation of extract led to identification of two subfractions with antitopoisomerase I and II activity at 154μg/mL (Positive controls 50 and 100μg/mL).
Conclusion: Methanol extracts of , , , and stems showed antitopoisomerase and non-mutagenic activities, and consequently could be promising as a source of anticancer drugs.
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http://dx.doi.org/10.21010/ajtcam.v14i3.7 | DOI Listing |
Toxicol In Vitro
December 2025
Departamento de Ingenierías Química y Bioquímica, Tecnológico Nacional de México/I.T. Morelia, Av. Tecnológico 1500, Col. Lomas de Santiaguito, Morelia CP 58120, Michoacán, Mexico.
Lupeol (LP), a bioactive triterpene, has been extensively studied for its chemoprotective, anti-inflammatory, and anti-arthritic properties. To enhance its bioavailability, lupeol-loaded polylactic-co-glycolic acid (PLGA) nanoparticles, designated T14, were developed using the emulsification-evaporation method. These nanoparticles exhibited an average size of 339.
View Article and Find Full Text PDFRSC Adv
July 2025
Chemistry Department, Faculty of Science, Port-Said University Port-Said Egypt
[This corrects the article DOI: 10.1039/D5RA00889A.].
View Article and Find Full Text PDFMolecules
June 2025
Univ. Limoges, LABCiS, UR 22722, Faculty of Pharmacy, F-87000 Limoges, France.
Cancer remains one of the leading causes of morbidity and mortality worldwide, driving the search for innovative and selective therapeutic agents. Topoisomerases I and II are essential enzymes involved in key cellular processes such as DNA replication and transcription. They have emerged as valuable anticancer targets; thus, many inhibitors of topoisomerases have been designed and some of them are considered to be major anticancer agents such as anthracyclines, etoposide or irinotecan.
View Article and Find Full Text PDFClin Exp Rheumatol
August 2025
Clinical and Research Section of Rheumatology and Clinical Immunology, Fondazione Policlinico Campus Biomedico, Rome; and Rheumatology and Clinical Immunology, Department of Medicine, University of Rome Campus Biomedico, School of Medicine, Rome, Italy.
Objectives: To evaluate the clinical, and serological features and treatments in two independent cohorts of Italian and Egyptian systemic sclerosis (SSc) patients, according to geographic areas.
Methods: 3 Italian and 5 Egyptian centres participated in patient recruitment in 2017. The demographic, clinical, and serological data were collected and defined according to the previously developed severity score and activity index.
RSC Adv
June 2025
Chemistry Department, Faculty of Science, Port-Said University Port-Said Egypt
A new ligand, benzylidene-phenol-thiazole (HBHTP), and its M(ii) complexes (M = Co, Ni, Cu, or Zn) were synthesized using a hybrid pharmacophore approach. The structures were optimized using density functional theory (DFT) calculations. MTT cytotoxicity assay showed that CuBHTP was the most effective and least toxic to normal cells, with the highest toxicity against MCF-7 cells.
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