HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Methanolic extract of Artemisia absinthium prompts apoptosis, enhancing expression of Bax/Bcl-2 ratio, cell cycle arrest, caspase-3 activation and mitochondrial membrane potential destruction in human colorectal cancer HCT-116 cells.

Abstract
The Artemisia absinthium (AA), belongs to the Asteraceae family, is used as a therapeutic agent in traditional medicine in Iran. It is a rich source of biology-active compounds. However, the molecular mechanism of AA contributing to cell proliferation and apoptosis is still unknown. This study aims to assess the anticancer activity of the methanolic extract of A. absinthium (MEAA) against human colorectal cancer HCT-116 cell line. The cytotoxic effects of MEAA on HCT-116 cells was evaluated by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium (MTT) assay. The expression levels of BAX and BCL-2 in HCT-116 cell line were examined by qRT-PCR. Annexin V/PI-flow cytometry technique was used to detect the cell cycle and apoptosis. MMP was predicted by Rhodamine 123 staining, and caspase 3 activity was analyzed by ELISA. Western blot method was performed to detect the expression level of BAX, Bcl-2 and Caspase-3 proteins. The MTT test revealed MEAA reduced the viability of HCT-116 cells. The mRNA and protein levels of BAX increased, but those of BCL-2 decreased in MEAA-treated cells. MEAA also prompted cell cycle arrest and induced apoptosis. After adding MEAA, the protein level and activity of caspase 3 and MMP destruction significantly increased. MEAA predominantly prompted apoptosis in HCT-116 cells by activating the mitochondrial pathway.
AuthorsMehri Nazeri, Asghar Mirzaie-Asl, Massoud Saidijam, Mohammadreza Moradi
JournalMolecular biology reports (Mol Biol Rep) Vol. 47 Issue 11 Pg. 8831-8840 (Nov 2020) ISSN: 1573-4978 [Electronic] Netherlands
PMID33141288 (Publication Type: Journal Article)
Chemical References
  • BCL2 protein, human
  • Plant Extracts
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein
  • Caspase 3
  • Methanol
Topics
  • Animals
  • Apoptosis (drug effects)
  • Artemisia absinthium (chemistry)
  • Caspase 3 (metabolism)
  • Cell Cycle Checkpoints (drug effects)
  • Cell Survival (drug effects)
  • Chlorocebus aethiops
  • Colorectal Neoplasms (genetics, metabolism, pathology)
  • Dose-Response Relationship, Drug
  • Enzyme Activation (drug effects)
  • Gene Expression Regulation, Neoplastic (drug effects)
  • HCT116 Cells
  • Humans
  • Membrane Potential, Mitochondrial (drug effects)
  • Methanol (chemistry)
  • Plant Extracts (pharmacology)
  • Proto-Oncogene Proteins c-bcl-2 (genetics, metabolism)
  • Vero Cells
  • bcl-2-Associated X Protein (genetics, metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: