4.6 Article

Anticancer Effects of Helminthostachys zeylanica Ethyl acetate Extracts on Human Gastric Cancer Cells through Downregulation of the TNF-α-activated COX-2-cPLA2-PGE2 Pathway

Journal

JOURNAL OF CANCER
Volume 12, Issue 23, Pages 7052-7068

Publisher

IVYSPRING INT PUBL
DOI: 10.7150/jca.64638

Keywords

Helminthostachys zeylanica; anti-inflammation; anticancer; gastric cancer

Categories

Funding

  1. Ministry of Science and Technology of Taiwan [MOST 109-2320-B-255-003-MY2]
  2. Chang Gung Memorial Hospital [CMRPF1I0031, CMRPF3L0031, BMRPD16]
  3. Chang Gung University of Science and Technology [ZRRPF3J0081-5, ZRRPF3J0081-7, ZRRPF3K0111-6, ZRRPF3K0111-10, ZRRPF3L0091-6, ZRRPF3L0091-10, ZMRPF3L0071]

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Our study found that the extract of Helminthostachys zeylanica (E2) has potential as a novel adjunctive agent for the treatment of gastric cancer by inducing apoptosis, increasing autophagy, inhibiting cell proliferation, cell cycle arrest, and suppressing cell migration in gastric cancer cells.
Background: Gastric cancer (GC) is the second most prevalent cancer worldwide and the eighth most common cause of tumor-related death in Taiwan. Helminthostachys zeylanica, a flavonoid compound, has anti-inflammatory, immunomodulatory, and anticancer effects. We examined whether an extract of H. zeylanica (E1 and E2) has potential as a treatment for GC. Methods: We investigated the effects (pro-apoptosis, pro-autophagy, and antiproliferation ability) of H. zeylanica-E2 on cell viability in healthy gastric epithelial (GES-1) and GC cells (AGS and BGC823). H. zeylanica-E2 was toxic to GC cells but had little or no toxicity to normal cells. Results: In this study, H. zeylanica-E2 induced apoptosis through caspase 3/7, Bcl-2, Bax, cyclooxygenase-2 (COX-2), and cleaved poly (ADP-ribose) polymerase pathways in GC cells. In addition, it increased autophagy by stimulating autophagy-related protein (ATG)5, ATG7, LC3-I/LC3-II, and inhibiting COX-2 activity in GC cells. We also found that H. zeylanica-E2 exhibited antiproliferation ability through cell cycle arrest in G0/G1 and G2/M and suppressed the migration of GC cells. The anticancer effects of H. zeylanica-E2 in GC cells might be mediated partly through inhibition of tumor necrosis factor-alpha (TNF-alpha)-activated proinflammatory cytosolic phospholipase A2 (cPLA2)-COX-2-prostaglandin E-2 (PGE(2)) pathway. Conclusions: Our results suggest that H. zeylanica-E2 has potential as a novel adjunctive agent for the treatment of GC.

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