Cytostatic and Anti-tumor Potential of Ajwa Date Pulp against Human Hepatocellular Carcinoma HepG2 Cells

Sci Rep. 2019 Jan 21;9(1):245. doi: 10.1038/s41598-018-36475-0.

Abstract

Ajwa dates (Phoenix dactylifera L.) are used by traditional therapeutic practitioners for several health benefits but most remain to be scientifically validated. In this study, we evaluated the apoptosis-inducing effect of ethanolic extract of Ajwa date pulp (ADP) on human hepatocellular carcinoma (HCC) HepG2 cells. High performance liquid chromatography analysis revealed the presence of polysaccharide β-D-glucan in ADP extract. Treated HCC cells revealed morphological characteristics of apoptosis under phase contrast microscopy. MTT assay demonstrated significant (p < 0.05) dose- and time-dependent inhibition of HCC cell growth. HCC cells were found to be in late apoptotic stage on treatment with higher doses of ADP extract as depicted by acridine orange/ethidium bromide and Annexin V-FITC/PI double stain. Importantly, ADP extract increased the reactive oxygen species level and decreased the mitochondrial membrane potential in treated HCC cells. Flow cytometry analysis demonstrated that ADP extract induced elevation of S and G2/M phases of cell cycle. Moreover, ADP extract induced apoptosis in HCC cells independent of tumor suppressor genes viz. CHEK2, ATM and TP53. Interestingly, ADP extract did not display any significant effect on normal cell line Vero. This study provides validation that ADP extract can be considered as a safe and natural potential drug candidate against human liver cancer.

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Apoptosis / drug effects
  • Carcinoma, Hepatocellular / drug therapy*
  • Cell Cycle Checkpoints / drug effects
  • Chlorocebus aethiops
  • Cytostatic Agents / pharmacology*
  • Hep G2 Cells
  • Humans
  • Liver Neoplasms / diet therapy*
  • Membrane Potential, Mitochondrial / drug effects
  • Phoeniceae / metabolism
  • Plant Extracts / pharmacology*
  • Proteoglycans
  • Reactive Oxygen Species / metabolism
  • Vero Cells
  • beta-Glucans / pharmacology*

Substances

  • Antineoplastic Agents, Phytogenic
  • Cytostatic Agents
  • Plant Extracts
  • Proteoglycans
  • Reactive Oxygen Species
  • beta-Glucans
  • polysaccharide-K