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Cytotoxic, Apoptosis-Inducing Activities, and Molecular Docking of a New Sterol from Bamboo Shoot Skin Phyllostachys heterocycla var. pubescens.
Abdelhameed, Reda F A; Nafie, Mohamed S; Ibrahim, Ahmed K; Yamada, Koji; Abdel-Kader, Maged S; Ibrahim, Amany K; Ahmed, Safwat A; Badr, Jihan M; Habib, Eman S.
Afiliación
  • Abdelhameed RFA; Department of Pharmacognosy, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.
  • Nafie MS; Department of Chemistry, Faculty of Science, Suez Canal University, Ismailia 41522, Egypt.
  • Ibrahim AK; Department of Pharmacognosy, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.
  • Yamada K; Garden for Medicinal Plants, Graduate School of Biomedical Sciences, Nagasaki University, Bunkyo-machi 1-14, Nagasaki 852-8521, Japan.
  • Abdel-Kader MS; Department of Pharmacognosy, College of Pharmacy, Prince Sattam Bin Abdulaziz University 173, Al-Kharj 11942, Saudi Arabia.
  • Ibrahim AK; Department of Pharmacognosy, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.
  • Ahmed SA; Department of Pharmacognosy, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.
  • Badr JM; Department of Pharmacognosy, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.
  • Habib ES; Department of Pharmacognosy, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.
Molecules ; 25(23)2020 Nov 30.
Article en En | MEDLINE | ID: mdl-33266171
ABSTRACT
Phytochemical screening of nonpolar fractions from the methanol extract of the Bamboo shoot skin Phyllostachys heterocycla var. pubescens resulted in the isolation of a new sterol-glucoside-fatty acid derivative (6'-O-octadeca-8'',11''-dienoyl)-sitosterol-3-O-ß-d-glucoside (1), together with six known compounds. The chemical structures of the pure isolated compounds were deduced based on different spectral data. The isolated compounds were assessed to determine their cytotoxic activity, and the results were confirmed by determining their apoptotic activity. Compound 1 was more cytotoxic against the MCF-7 cells (IC50 = 25.8 µM) compared to Fluorouracil (5-FU) (26.98 µM), and it significantly stimulated apoptotic breast cancer cell death with 32.6-fold (16.63% compared to 0.51 for the control) at pre-G1 and G2/M-phase cell cycle arrest and blocked the progression of MCF-7 cells. Additionally, RT-PCR results further confirmed the apoptotic activity of compound 1 by the upregulation of proapoptotic genes (P53; Bax; and caspases 3, 8, and 9) and downregulation of the antiapoptotic genes (BCL2). Finally, the identified compounds, especially 1, were found to have high binding affinity towards both tyrosine-specific protein kinase (TPK) and vascular endothelial growth factor receptor (VEGFR-2) through the molecular docking studies that highlight its mode of action.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Esteroles / Neoplasias de la Mama / Apoptosis / Brotes de la Planta / Bambusa / Antineoplásicos Fitogénicos Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Egipto

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Esteroles / Neoplasias de la Mama / Apoptosis / Brotes de la Planta / Bambusa / Antineoplásicos Fitogénicos Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Egipto