4.5 Article

Essential Oil from Bark of Aniba parviflora (Meisn.) Mez (Lauraceae) Reduces HepG2 Cell Proliferation and Inhibits Tumor Development in a Xenograft Model

期刊

CHEMISTRY & BIODIVERSITY
卷 18, 期 3, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbdv.202000938

关键词

Aniba parviflora; antitumor agents; cytotoxicity; HepG2; Lauraceae

资金

  1. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq, Brazil)
  2. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES, Brazil) [001]
  3. Fundacao de Amparo a Pesquisa do Estado da Bahia (FAPESB, Brazil)
  4. Fundacao de Amparo a Pesquisa do Estado do Amazonas (FAPEAM, Brazil)

向作者/读者索取更多资源

Aniba parviflora is an aromatic plant from the Amazon rainforest with commercial value in the perfumery industry, and is traditionally used in Brazilian folk medicine to treat snakebites. The essential oil extracted from its bark demonstrated significant growth inhibition on human hepatocellular carcinoma cells (HepG2) with minimal toxicity to non-cancerous cells.
Aniba parviflora (Meisn.) Mez (Lauraceae) is an aromatic plant of the Amazon rainforest, which has a tremendous commercial value in the perfumery industry; it is popularly used as flavoring sachets and aromatic baths. In Brazilian folk medicine, A. parviflora is used to treat victims of snakebites. Herein, we analyzed the chemical composition of A. parviflora bark essential oil (EO) and its effect on the growth of human hepatocellular carcinoma HepG2 cells in vitro and in vivo. EO was obtained by hydrodistillation and characterized by GC-MS and GC-FID. The main constituents of EO were linalool (16.3 +/- 3.15), alpha-humulene (14.5 +/- 2.41 %), delta-cadinene (10.2 +/- 1.09 %), alpha-copaene (9.51 +/- 1.12 %) and germacrene B (7.58 +/- 2.15 %). Initially, EO's cytotoxic effect was evaluated against five cancer cell lines (HepG2, MCF-7, HCT116, HL-60 and B16-F10) and one non-cancerous one (MRC-5), using the Alamar blue method after 72 h of treatment. The calculated IC50 values were 9.05, 22.04, >50, 15.36, 17.57, and 30.46 mu g/mL, respectively. The best selectivity was for HepG2 cells with a selective index of 3.4. DNA Fragmentation and cell cycle distribution were quantified in HepG2 cells by flow cytometry after a treatment period of 24 and 48 h. The effect of EO on tumor development in vivo was evaluated in a xenograft model using C.B-17 SCID mice engrafted with HepG2 cells. In vivo tumor growth inhibition of HepG2 xenograft at the doses of 40 and 80 mg/kg were 12.1 and 62.4 %, respectively.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据