4.6 Article

Duguetia pycnastera Sandwith (Annonaceae) Leaf Essential Oil Inhibits HepG2 Cell Growth In Vitro and In Vivo

期刊

MOLECULES
卷 27, 期 17, 页码 -

出版社

MDPI
DOI: 10.3390/molecules27175664

关键词

Duguetia pycnastera; essential oil; HepG2 cells; cytotoxic; antitumor

资金

  1. Brazilian agency Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)
  2. Brazilian agency Fundacao de Amparo a Pesquisa do Estado do Amazonas (FAPEAM)
  3. Brazilian agency Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)
  4. Brazilian agency CNPq/INCT [465357/2014]

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In this study, the inhibitory effects of D. pycnastera leaf essential oil on the growth of liver cancer cells were investigated both in vitro and in vivo. The results showed that the oil exhibited cytotoxicity and also inhibited tumor mass growth in vivo.
Duguetia pycnastera Sandwith (Annonaceae) is a tropical tree that can be found in the Guyanas, Bolivia, Venezuela, and Brazil. In Brazil, it is popularly known as ata, envira, envira-preta, and envira-surucucu. In the present work, we investigated the in vitro and in vivo HepG2 cell growth inhibition capacity of D. pycnastera leaf essential oil (EO). The chemical composition of the EO was determined by GC-MS and GC-FID analyses. The alamar blue assay was used to examine the in vitro cytotoxicity of EO in cancer cell lines and non-cancerous cells. In EO-treated HepG2 cells, DNA fragmentation was measured by flow cytometry. The in vivo antitumor activity of the EO was assessed in C.B-17 SCID mice xenografted with HepG2 cells treated with the EO at a dosage of 40 mg/kg. Chemical composition analysis displayed the sesquiterpenes alpha-gurjunene (26.83%), bicyclogermacrene (24.90%), germacrene D (15.35%), and spathulenol (12.97%) as the main EO constituents. The EO exhibited cytotoxicity, with IC50 values ranging from 3.28 to 39.39 mu g/mL in the cancer cell lines SCC4 and CAL27, respectively. The cytotoxic activity of the EO in non-cancerous cells revealed IC50 values of 16.57, 21.28, and >50 mu g/mL for MRC-5, PBMC, and BJ cells, respectively. An increase of the fragmented DNA content was observed in EO-treated HepG2 cells. In vivo, EO displayed tumor mass inhibition activity by 47.76%. These findings imply that D. pycnastera leaf EO may have anti-liver cancer properties.

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