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二十二碳六烯酸通过调节谷胱甘肽水平和抑制核苷酸合成抑制 Kras/TP53 双突变胰腺导管腺癌细胞的增殖。

Docosahexaenoic acid inhibits the proliferation of Kras/TP53 double mutant pancreatic ductal adenocarcinoma cells through modulation of glutathione level and suppression of nucleotide synthesis.

机构信息

Biomedical Science Laboratory, Department of Nutrition, China Medical University, Taichung, Taiwan, Republic of China.

Graduate Institute of Integrated Medicine, China Medical University, Taichung, Taiwan, Republic of China.

出版信息

PLoS One. 2020 Nov 2;15(11):e0241186. doi: 10.1371/journal.pone.0241186. eCollection 2020.

Abstract

The treatment of cancer cells obtained by blocking cellular metabolism has received a lot of attention recently. Previous studies have demonstrated that Kras mutation-mediated abnormal glucose metabolism would lead to an aberrant cell proliferation in human pancreatic ductal adenocarcinoma (PDAC) cells. Previous literature has suggested that consumption of fish oil is associated with lower risk of pancreatic cancer. In this study, we investigated the anti-cancer effects of docosahexaenoic acid (DHA) in human PDAC cells in vitro and in vivo. Omega-3 polyunsaturated fatty acids (PUFAs) such as DHA and eicosapentaenoic acid (EPA) significantly inhibited the proliferation of human PDAC cells. The actions of DHA were evaluated through an induction of cell cycle arrest at G1 phase and noticed a decreased expression of cyclin A, cyclin E and cyclin B proteins in HPAF-II cells. Moreover, it was found that co-treatment of DHA and gemcitabine (GEM) effectively induced oxidative stress and cell death in HPAF-II cells. Interestingly, DHA leads to an increased oxidative glutathione /reduced glutathione (GSSG/GSH) ratio and induced cell apoptosis in HPAF-II cells. The findings in the study showed that supplementation of GSH or N-Acetyl Cysteine (NAC) could reverse DHA-mediated cell death in HPAF-II cells. Additionally, DHA significantly increased cellular level of cysteine, cellular NADP/NADPH ratio and the expression of cystathionase (CTH) and SLCA11/xCT antiporter proteins in HPAF-II cells. The action of DHA was, in part, associated with the inactivation of STAT3 cascade in HPAF-II cells. Treatment with xCT inhibitors, such as erastin or sulfasalazine (SSZ), inhibited the cell survival ability in DHA-treated HPAF-II cells. DHA also inhibited nucleotide synthesis in HPAF-II cells. It was demonstrated in a mouse-xenograft model that consumption of fish oil significantly inhibited the growth of pancreatic adenocarcinoma and decreased cellular nucleotide level in tumor tissues. Furthermore, fish oil consumption induced an increment of GSSG/GSH ratio, an upregulation of xCT and CTH proteins in tumor tissues. In conclusion, DHA significantly inhibited survival of PDAC cells both in vitro and in vivo through its recently identified novel mode of action, including an increment in the ratio of GSSG/GSH and NADP/NADPH respectively, and promoting reduction in the levels of nucleotide synthesis.

摘要

最近,通过阻断细胞代谢来治疗癌细胞受到了广泛关注。先前的研究表明,Kras 突变介导的异常葡萄糖代谢会导致人类胰腺导管腺癌 (PDAC) 细胞异常增殖。先前的文献表明,食用鱼油与降低胰腺癌风险有关。在这项研究中,我们研究了二十二碳六烯酸 (DHA) 在体外和体内对人 PDAC 细胞的抗癌作用。ω-3 多不饱和脂肪酸 (PUFA),如 DHA 和二十碳五烯酸 (EPA),显著抑制人 PDAC 细胞的增殖。通过诱导细胞周期停滞在 G1 期,评估了 DHA 的作用,并注意到 HPAF-II 细胞中环蛋白 A、E 和 B 蛋白的表达降低。此外,研究发现 DHA 与吉西他滨 (GEM) 联合治疗可有效诱导 HPAF-II 细胞发生氧化应激和细胞死亡。有趣的是,DHA 导致氧化型谷胱甘肽/还原型谷胱甘肽 (GSSG/GSH) 比值增加,并诱导 HPAF-II 细胞凋亡。研究结果表明,在 HPAF-II 细胞中补充谷胱甘肽或 N-乙酰半胱氨酸 (NAC) 可逆转 DHA 介导的细胞死亡。此外,DHA 显著增加了 HPAF-II 细胞中半胱氨酸的细胞内水平、细胞内 NADP/NADPH 比值以及胱硫醚 (CTH) 和 SLCA11/xCT 转运蛋白的表达。DHA 的作用部分与 HPAF-II 细胞中 STAT3 级联的失活有关。用 xCT 抑制剂,如 erastin 或柳氮磺胺吡啶 (SSZ),处理 HPAF-II 细胞,可抑制 DHA 处理后的细胞存活能力。DHA 还抑制 HPAF-II 细胞中的核苷酸合成。在小鼠异种移植模型中,食用鱼油可显著抑制胰腺腺癌的生长,并降低肿瘤组织中的细胞核苷酸水平。此外,食用鱼油可诱导肿瘤组织中 GSSG/GSH 比值增加,xCT 和 CTH 蛋白表达上调。总之,DHA 通过其最近确定的新型作用机制,包括 GSSG/GSH 比值和 NADP/NADPH 比值的增加,以及促进核苷酸合成水平的降低,显著抑制了 PDAC 细胞在体外和体内的存活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c82/7605869/9cc0ae019f3e/pone.0241186.g001.jpg

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