The inhibitory effect of Gleditsia sinensis on cyclooxygenase-2 expression in human esophageal squamous cell

K C Pak1, K Y Lam, S Law

  • 1Lo Ka Chung Centre for Natural Anti-cancer Drug Development, The Hong Kong Polytechnic University, Hong Kong SAR, P.R. China.

Insights

Gleditsia sinensis extract (GSE) shows anti-cancer effects against esophageal squamous cell carcinoma (ESCC) by reducing cyclooxygenase-2 (COX-2) expression. This study highlights GSE

Area of Science:

  • Oncology
  • Pharmacology
  • Molecular Biology

Background:

  • Previous research established Gleditsia sinensis extract (GSE) exhibits anti-cancer properties via apoptosis, telomerase inhibition, and anti-angiogenesis.
  • Cyclooxygenase-2 (COX-2) is a validated therapeutic target for esophageal squamous cell carcinoma (ESCC), necessitating novel agents targeting its expression.
  • The impact of GSE on COX-2 expression in ESCC has not been previously explored.

Purpose of the Study:

  • To investigate the anti-cancer effects of GSE on multiple ESCC cell lines.
  • To determine if GSE modulates the expression of COX-2 and COX-1 in ESCC cells.
  • To evaluate the anti-proliferative potential of GSE in ESCC.

Main Methods:

  • MTS cytotoxicity assays were performed on eight ESCC cell lines.
  • Multiplex RT-PCR analysis was used to assess COX-2 and COX-1 mRNA expression levels.
  • Anchorage-independent clonogenicity assays in soft agar evaluated the anti-proliferative effect on KYSE 510 cells.

Main Results:

  • GSE demonstrated dose- and time-dependent cytotoxicity against all eight ESCC cell lines.
  • GSE significantly suppressed COX-2 mRNA expression in a dose-dependent manner across all tested ESCC cell lines, while COX-1 expression remained unaffected.
  • GSE exhibited anti-proliferative activity in the anchorage-independent clonogenicity assay, indicating suppressed in vitro growth of ESCC cells.

Conclusions:

  • The anti-cancer effects of GSE against ESCC cell lines are associated with the suppression of COX-2 expression.
  • GSE does not appear to affect COX-1 expression in these ESCC models.
  • These findings support the potential of GSE as a novel anti-cancer agent or as an adjunct therapy for ESCC.