College of Medicine and Public Health, Ubon Ratchathani University, 85 Sathonmak Road, Warinchamrap, Ubon Ratchathani, Thailand.
Asian Pac J Cancer Prev. 2022 Apr 1;23(4):1351-1358. doi: 10.31557/APJCP.2022.23.4.1351.
To examine the effects of ibuprofen, naproxen and diclofenac, non-steroidal anti-inflammatory drugs (NSAIDs) on cell proliferation activity of the human CCA cell lines.
KKU-M139 and KKU-213B cell lines were used in this study. The cell viability was assessed by the MTT assay. Lipid synthesis determined by Oil red O staining and colorimetric assay. An inverted phase-contrast light microscope was used to investigate the histological change of the cells. Caspases 3/7 activity and AnnexinV/PI were used to assess apoptosis by multiple microplate reader.
The results showed that ibuprofen, naproxen and diclofenac suppressed the viability of the KKU-M139 and KKU-213B cells in a dose-dependent manner, as measured especially diclofenac. However, these three NSAIDs slightly decreased lipid synthesis determined by Oil red O staining and colorimetric assay. The histological change observations showed the shrinking cell and become star-shaped in high dose treated groups. Interestingly, these NSAIDs exhibited in both of KKU-M139 and KKU-213B cell lines, the diclofenac-treated cells had the most injury cells. The cells exhibited cell injury features. In addition, the detection of caspase 3/7 and AnnexinV/PI in this investigation revealed early cell apoptotic characteristics.
These finding suggest that ibuprofen, naproxen and diclofenac suppress cell viability. The results reveal that ibuprofen, naproxen and diclofenac, which induce the histological change and apoptosis. This study indicates that these NSAIDs may be used as an anti-proliferation agent for the treatment of CCA in the future.
研究布洛芬、萘普生和双氯芬酸这 3 种非甾体抗炎药(NSAIDs)对人 CCA 细胞系细胞增殖活性的影响。
本研究使用了 KKU-M139 和 KKU-213B 细胞系。通过 MTT 测定法评估细胞活力。用油红 O 染色和比色法测定脂质合成。倒置相差显微镜用于观察细胞的组织学变化。通过多微孔板读取器评估 caspase 3/7 活性和 AnnexinV/PI 以评估细胞凋亡。
结果表明,布洛芬、萘普生和双氯芬酸均以剂量依赖性方式抑制 KKU-M139 和 KKU-213B 细胞的活力,尤其是双氯芬酸。然而,这 3 种 NSAIDs 略微降低了油红 O 染色和比色法测定的脂质合成。组织学变化观察显示,高剂量处理组的细胞收缩并呈星形。有趣的是,这些 NSAIDs 在 KKU-M139 和 KKU-213B 细胞系中均表现出,双氯芬酸处理的细胞中损伤细胞最多。这些细胞表现出细胞损伤特征。此外,本研究中 caspase 3/7 和 AnnexinV/PI 的检测显示出早期细胞凋亡特征。
这些发现表明布洛芬、萘普生和双氯芬酸抑制细胞活力。结果表明,布洛芬、萘普生和双氯芬酸诱导组织学变化和细胞凋亡。本研究表明,这些 NSAIDs 将来可能被用作治疗 CCA 的增殖抑制剂。