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Published on: December 23, 2022
The inhibitory effect of Gleditsia sinensis on cyclooxygenase-2 expression in human esophageal squamous cell
1Lo Ka Chung Centre for Natural Anti-cancer Drug Development, The Hong Kong Polytechnic University, Hong Kong SAR, P.R. China.
Abstract:
The anti-cancer effects of the anomalous fruit extract of Gleditsia sinensis (GSE) attributed to its apoptotic activity, telomerase inhibition and anti-angiogenesis in a panel of solid and non-solid tumor cell lines including esophageal squamous cell carcinoma (ESCC) have been intensively investigated by us in previous studies. Cyclooxygenase-2 (COX-2) has been well described as another promising target of cancer therapy for ESCC, and novel therapeutic agents are still being sought which target COX-2 expression. However, the anti-cancer effect of GSE through the suppression of COX-2 expression has not been previously investigated. In the present study, the anti-cancer effects of GSE on eight ESCC cell lines (KYSE 30, KYSE 150, KYSE 450, KYSE 510, KYSE 520, HKESC-3, HKESC-4 and SLMT-1) of Chinese and Japanese origins were first studied by MTS cytotoxicity assays. The effects of GSE on COX-2 expression levels and on the housekeeping form COX-1 were also investigated by multiplex RT-PCR analysis. Moreover, the anti-proliferative effect of GSE on KYSE 510 was also studied by anchorage-independent clonogenicity assay in soft agar. The results showed that GSE induced a dose- and time-dependent cytotoxicity on all of the eight ESCC cell lines and caused positive anti-proliferative action on KYSE 510 in the anchorage-independent clonogenicity assay, suggesting that GSE suppressed the in vitro growth of the ESCC cell lines. More importantly, the MRNA expression levels of COX-2, but not COX-1, in all of the ESCC cell lines were suppressed by GSE in a dose-dependent fashion. The overall results of the present study show that the anti-cancer effect of GSE on the ESCC cell lines is associated with the suppression of COX-2 expression, but not COX-1. Our findings also open a new chapter for the future advancement of GSE as a novel anti-cancer agent or as an adjuvant of traditional cancer treatments.
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.
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