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香豆酸、山奈酚、芦丁和梓醇苷影响 AGS 胃癌细胞糖型的表达。

-Coumaric acid, Kaempferol, Astragalin and Tiliroside Influence the Expression of Glycoforms in AGS Gastric Cancer Cells.

机构信息

Department of Medical Chemistry, Faculty of Pharmacy, Medical University of Białystok, ul. Mickiewicza 2a, 15-222 Białystok, Poland.

Department of Pharmacognosy, Faculty of Pharmacy, Medical University of Białystok, ul. Mickiewicza 2a, 15-222 Białystok, Poland.

出版信息

Int J Mol Sci. 2022 Aug 2;23(15):8602. doi: 10.3390/ijms23158602.

Abstract

Abnormal glycosylation of cancer cells is considered a key factor of carcinogenesis related to growth, proliferation, migration and invasion of tumor cells. Many plant-based polyphenolic compounds reveal potential anti-cancer properties effecting cellular signaling systems. Herein, we assessed the effects of phenolic acid, -coumaric acid and flavonoids such as kaempferol, astragalin or tiliroside on expression of selected cancer-related glycoforms and enzymes involved in their formation in AGS gastric cancer cells. The cells were treated with 80 and 160 µM of the compounds. RT-PCR, Western blotting and ELISA tests were performed to determine the influence of polyphenolics on analyzed factors. All the examined compounds inhibited the expression of MUC1, ST6GalNAcT2 and FUT4 mRNAs. C1GalT1, St3Gal-IV and FUT4 proteins as well as MUC1 domain, Tn and sialyl T antigen detected in cell lysates were also lowered. Both concentrations of kaempferol, astragalin and tiliroside also suppressed ppGalNAcT2 and C1GalT1 mRNAs. MUC1 cytoplasmic domain, sialyl Tn, T antigens in cell lysates and sialyl T in culture medium were inhibited only by kaempferol and tiliroside. Nuclear factor NF-κB mRNA expression decreased after treatment with both concentrations of kaempferol, astragalin and tiliroside. NF-κB protein expression was inhibited by kaempferol and tiliroside. The results indicate the rationality of application of examined polyphenolics as potential preventive agents against gastric cancer development.

摘要

癌细胞的异常糖基化被认为是与肿瘤细胞的生长、增殖、迁移和侵袭相关的致癌作用的关键因素。许多植物来源的多酚化合物显示出潜在的抗癌特性,影响细胞信号系统。在此,我们评估了酚酸、-阿魏酸和黄酮类化合物(如山柰酚、黄芪苷或桃叶珊瑚苷)对AGS 胃癌细胞中选定的与癌症相关的糖型和参与其形成的酶的表达的影响。用 80 和 160 μM 的化合物处理细胞。进行 RT-PCR、Western blot 和 ELISA 试验,以确定多酚对分析因素的影响。所有检查的化合物均抑制 MUC1、ST6GalNAcT2 和 FUT4 mRNA 的表达。细胞裂解物中检测到的 C1GalT1、St3Gal-IV 和 FUT4 蛋白以及 MUC1 结构域、Tn 和唾液酸化 T 抗原也降低。两种浓度的山柰酚、黄芪苷和桃叶珊瑚苷也抑制了 ppGalNAcT2 和 C1GalT1 mRNA 的表达。MUC1 细胞质结构域、细胞裂解物中的唾液酸化 Tn、T 抗原和培养基中的唾液酸化 T 仅被山柰酚和桃叶珊瑚苷抑制。用两种浓度的山柰酚、黄芪苷和桃叶珊瑚苷处理后,核因子 NF-κB mRNA 的表达降低。NF-κB 蛋白表达被山柰酚和桃叶珊瑚苷抑制。这些结果表明,检查的多酚作为预防胃癌发展的潜在预防剂的应用具有合理性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a78a/9369150/8f3322aa2dae/ijms-23-08602-g001.jpg

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