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Curcumin Has Anti-Proliferative and Pro-Apoptotic Effects on Tongue Cancer in vitro: A Study with Bioinformatics Analysis and in vitro Experiments

机译:姜黄素对体外舌癌具有抗增殖和促凋亡作用:具有生物信息学分析和体外实验的研究

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Purpose: This study focused on the mechanism underlying the therapeutic effect of curcumin against tongue cancer (TC). Methods: Target genes of TC and curcumin were identified, respectively. Three datasets of TC from Gene Expression Omnibus were included, and then the differentially expressed genes were collected. After combing the data from The Cancer Genome Atlas, bioinformatics analyses were performed to investigate hub genes in terms of the functions and correlations. The proliferation and migration of TC cells were evaluated with CCK-8 assay and scratch wound healing assay, respectively. Cell apoptosis was evaluated by TUNEL assay, flow cytometry and Western blot. Cell cycle was determined by flow cytometry. Results: In this study, 15 hub genes were identified (TK1, TDRD3, TAGLN2, RNASEH2A, PDE2A, NCF2, MAP3K3, GPX3, GPD1L, GBP1, ENO1, CAT, ALDH6A1, AGPS and ACACB). They were mainly enriched in oxygen-related processes, such as oxidation-reduction process, reactive oxygen species metabolic process, hydrogen peroxide catabolic process, oxidoreductase activity and Peroxisome-related pathway. The expression levels of hub gene mRNAs were positively correlated with each other’s expression levels. None of the hub genes was correlated with prognosis ( P 0.05). Curcumin significantly inhibited CAL 27 cell proliferation and migration ( P 0.05), but significantly promoted cell apoptosis ( P 0.05). Conclusion: Curcumin has potential therapeutic effect on treating TC by suppressing cell proliferation and migration, as well as promoting apoptosis through modulating oxygen-related signaling pathways.
机译:目的:本研究重点是姜黄素对舌癌(TC)治疗效果的机制。方法:分别鉴定了Tc和姜黄素的靶基因。包括来自基因表达综合的三种TC的数据集,然后收集差异表达的基因。从癌症基因组Atlas梳理数据后,进行生物信息学分析以在功能和相关性方面进行枢纽基因。用CCK-8测定和划伤伤口愈合测定评估TC细胞的增殖和迁移。通过TUNEL测定,流式细胞术和Western印迹评估细胞凋亡。通过流式细胞术确定细胞周期。结果:在该研究中,鉴定了15个轮毂基因(TK1,TDRD3,TaglN2,RNASEH2A,PDE2A,NCF2,MAP3K3,GPX3,GPD1L,GBP1,ENO1,CAT,ALDH6A1,AGPS和ACACB)。它们主要富含氧相关的方法,例如氧化还原过程,反应性氧物种代谢过程,过氧化氢分解法,氧化还原酶活性和过氧化物组织相关途径。轮毂基因MRNA的表达水平与彼此的表达水平正相关。枢纽基因没有任何预后(P> 0.05)。姜黄素显着抑制CAL 27细胞增殖和迁移(P <0.05),但显着促进细胞凋亡(P <0.05)。结论:姜黄素通过抑制细胞增殖和迁移来治疗TC的潜在治疗效果,以及通过调节氧相关的信号通路来促进细胞凋亡。

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