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1.
Biomed Pharmacother ; 118: 109278, 2019 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-31387004

RESUMO

Gastric cancer is a common oncological disease. Although enormous efforts have been expended, possible therapeutic modalities are still limited. For this reason, new therapeutic approaches and agents are highly requested and intensively developed. One strategy is the application of natural agents, such as curcumin, with proven anticancer effects and low toxicity for patients. Therefore, this review discusses the potential application of curcumin in the therapy of gastric cancer and its potential incorporation in therapeutic regimens. Because one of the largest impediments for widespread curcumin application is its limited bioavailability (caused mainly by its very low water solubility), studied strategies (drug delivery systems and curcumin derivatization) aimed to solve this obstacle are discussed in more detail.


Assuntos
Curcumina/uso terapêutico , Neoplasias Gástricas/tratamento farmacológico , Animais , Curcumina/química , Sistemas de Liberação de Medicamentos , Humanos , Modelos Biológicos , Resultado do Tratamento
2.
Bioorg Chem ; 88: 102809, 2019 07.
Artigo em Inglês | MEDLINE | ID: mdl-30999246

RESUMO

Ten-eleven translocation protein (TET) 1 plays a key role in control of DNA demethylation and thereby of gene expression. Dysregulation of these processes leads to serious pathological states such as oncological and neurodegenerative ones and thus TET 1 targeting is highly requested. Therefore, in this work, we examined the ability of hydrazones (acyl-, aroyl- and heterocyclic hydrazones) to inhibit the TET 1 protein and its mechanism of action. Inhibitory activity of hydrazones 1-7 towards TET 1 was measured. The results showed a high affinity of the tested chelators for iron(II). The study clearly showed a significant correlation between the chelator's affinity for iron(II) ions (represented by the binding constant) and TET 1 protein inhibitory activity (represented by IC50 values).


Assuntos
Dioxigenases/antagonistas & inibidores , Inibidores Enzimáticos/química , Hidrazonas/química , Quelantes de Ferro/química , Dioxigenases/química , Ensaios Enzimáticos , Inibidores Enzimáticos/síntese química , Inibidores Enzimáticos/toxicidade , Epigênese Genética/efeitos dos fármacos , Hidrazonas/síntese química , Hidrazonas/toxicidade , Ferro/química , Quelantes de Ferro/síntese química , Quelantes de Ferro/toxicidade
3.
Curr Med Chem ; 26(20): 3812-3834, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-29600749

RESUMO

Filamentous ascomycetes (Neurospora and Monascus) have been studied for a long time because of their production of secondary metabolites such as microbial pigments. The ascomycetes represent an interesting group of compounds with high potential for medicinal applications. Many recent studies have shown their efficacy in the treatment of serious pathological states such as oncological diseases, neurodegenerative diseases and hyperlipidaemia. Nevertheless, the clinical usability of ascomycetes is still limited. However, this problem can be solved by the use of these compounds with combinations of other therapeutic agents. This strategy can suppress their side effects and improve their therapeutic efficacy. Moreover, their co-application can significantly enhance conventional therapies that are used. This review summarizes and discusses the general principles of this approach, introduced and supported by numerous examples. In addition, the prediction of the future potential application of this methodology is included.


Assuntos
Ascomicetos/química , Ascomicetos/metabolismo , Pigmentos Biológicos/metabolismo , Pigmentos Biológicos/uso terapêutico , Animais , Quimioterapia Combinada , Humanos
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