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梓醇苷——一种环烯醚萜苷,通过靶向PI3K/AKT信号通路、诱导凋亡以及抑制细胞迁移和侵袭,对耐药性人口腔癌细胞发挥抗增殖作用。

Kutkoside-an iridoid glycoside, exerts anti-proliferative effects in drug-resistant human oral carcinoma cells by targeting PI3K/AKT signalling pathway, inducing apoptosis and suppressing cell migration and invasion.

作者信息

Hou Jun-Chi, Xu Xiao Nan

机构信息

Department of Stomatology, Jining No.1 People's Hospital, Jining 272000 , Shandong, China.

出版信息

J BUON. 2020 Jan-Feb;25(1):338-343.

Abstract

PURPOSE

The main purpose of the current research work was to investigate the anticancer potential of Kutkoside -a naturally occurring iridoid glycoside, against drug-resistant human oral carcinoma cells along with evaluating its effects on PI3K/AKT signalling pathway, cellular apoptosis, cell migration and cell invasion.

METHODS

Cell viability was assessed by using MTT colorimetric assay, while effects on cellular apoptosis were evaluated by acridine orange (AO)/ethidium bromide (EB) as well as by using flow cytometry employing annexin V-FITC. Effects on cell migration and cell invasion were evaluated by in vitro wound healing assay and transwell Matrigel assay. Effects on PI3K/AKT signalling pathway were evaluated by western blot method.

RESULTS

Kutkoside led to significant and dose-dependent inhibition of HSC-2 human oral cancer cells using doses of 0, 1.25, 2.5, 5, 10, 20, 40, 80 and 160 μM. Fluorescence microscopy revealed that on increasing the dose of kutkoside, the number of both apoptotic and necrotic cells increased, showing that Kutkoside induces apoptotic cell death in HSC-2 oral cancer cell line in dose-dependent manner. Flow cytometry indicated that the percentage of apoptotic cells at different dose exposures of Kutkoside, namely 0, 8, 16 and 32 μM was 4.9%, 12.18%, 22.18% and 34.10%, respectively. Kutkoside treatment also led to cell migration inhibition and cell invasion inhibition. This molecule upregulated the expression of AKT and PI3K, simultaneously downregulating the expressions of p-AKT and p-PI3K in a dose-dependent manner.

CONCLUSION

Kutkoside shows potential anticancer and pro-apoptotic effects in HSC-2 oral carcinoma cells and as such may be developed as a possible anticancer agent provided further studies are performed.

摘要

目的

本研究工作的主要目的是研究马钱苷——一种天然存在的环烯醚萜苷,对耐药性人口腔癌细胞的抗癌潜力,并评估其对PI3K/AKT信号通路、细胞凋亡、细胞迁移和细胞侵袭的影响。

方法

采用MTT比色法评估细胞活力,而通过吖啶橙(AO)/溴化乙锭(EB)以及使用膜联蛋白V-FITC的流式细胞术评估对细胞凋亡的影响。通过体外伤口愈合试验和Transwell Matrigel试验评估对细胞迁移和细胞侵袭的影响。通过蛋白质印迹法评估对PI3K/AKT信号通路的影响。

结果

使用0、1.25、2.5、5、10、20、40、80和160μM的剂量,马钱苷导致HSC-2人口腔癌细胞显著且剂量依赖性的抑制。荧光显微镜显示,随着马钱苷剂量的增加,凋亡细胞和坏死细胞数量均增加,表明马钱苷以剂量依赖性方式诱导HSC-2口腔癌细胞系中的凋亡细胞死亡。流式细胞术表明,在马钱苷不同剂量暴露下,即0、8、16和32μM时,凋亡细胞的百分比分别为4.9%、12.18%、22.18%和34.10%。马钱苷处理还导致细胞迁移抑制和细胞侵袭抑制。该分子上调AKT和PI3K的表达,同时以剂量依赖性方式下调p-AKT和p-PI3K的表达。

结论

马钱苷在HSC-2口腔癌细胞中显示出潜在的抗癌和促凋亡作用,因此如果进行进一步研究,可能会被开发为一种潜在的抗癌药物。

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