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Chamuangone from Garcinia cowa leaves inhibits cell proliferation and migration and induces cell apoptosis in human cervical cancer in vitro.
Sae-Lim, Pirunrat; Seetaha, Supaphorn; Tabtimmai, Lueacha; Suphakun, Prapasiri; Kiriwan, Duangnapa; Panichayupakaranant, Pharkphoom; Choowongkomon, Kiattawee.
Afiliación
  • Sae-Lim P; Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat, Thailand.
  • Seetaha S; Phytomedicine and Pharmaceutical Biotechnology Excellence Center, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat-Yai, Thailand.
  • Tabtimmai L; Department of Biochemistry, Faculty of Science, Kasetsart University, Bangkok, Thailand.
  • Suphakun P; Center for Advanced Studies in Nanotechnology for Chemical, Food and Agricultural Industries, KU Institute for Advanced Studies, Kasetsart University, Bangkok, Thailand.
  • Kiriwan D; Department of Biochemistry, Faculty of Science, Kasetsart University, Bangkok, Thailand.
  • Panichayupakaranant P; Department of Biochemistry, Faculty of Science, Kasetsart University, Bangkok, Thailand.
  • Choowongkomon K; Genetic Engineering Interdisciplinary Program, Graduate School, Kasetsart University, Bangkok, Thailand.
J Pharm Pharmacol ; 72(3): 470-480, 2020 Mar.
Article en En | MEDLINE | ID: mdl-31875979
OBJECTIVES: To examine the effects of chamuangone on human cancer cell proliferation, migration and apoptosis. METHODS: An MTT assay was used to study the effect of chamuangone on human cervical carcinoma cell growth. An in-vitro scratch migration assay was used to investigate the activity of cell motility after chamuangone treatment. Chamuangone-induced cell apoptosis in HeLa cells was determined using the apoptotic assay kit. The inhibitory activities of chamuangone were examined by ADP-Glo™ kinase assay. The GOLD docking algorithm was used to demonstrate the mechanism against tyrosine kinase of EGFR. KEY FINDINGS: Chamuangone showed a strong inhibitory cell proliferation of HeLa cells with IC50 values of 3.59 µm and effectively inhibited HeLa cell migration. In addition, chamuangone exhibited the apoptotic cell death induction in a time and dose-dependent manner. Finally, chamuangone also was tested for EGFR-TK inhibition activity. The IC50 value of chamuangone was 2.85 nm, whereas the IC50 value of gefitinib was 15.10 nm. CONCLUSIONS: The above results confirm the inhibitory effects of chamuangone on HeLa cell proliferation and cell migration. In addition, chamuangone also induces cell apoptosis in HeLa cells. These findings indicate that chamuangone is a compound that is a potential chemotherapeutic agent.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Extractos Vegetales / Movimiento Celular / Neoplasias del Cuello Uterino / Apoptosis / Garcinia / Proliferación Celular Límite: Female / Humans Idioma: En Revista: J Pharm Pharmacol Año: 2020 Tipo del documento: Article País de afiliación: Tailandia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Extractos Vegetales / Movimiento Celular / Neoplasias del Cuello Uterino / Apoptosis / Garcinia / Proliferación Celular Límite: Female / Humans Idioma: En Revista: J Pharm Pharmacol Año: 2020 Tipo del documento: Article País de afiliación: Tailandia Pais de publicación: Reino Unido