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β-紫罗兰酮通过 GSK-3β 信号通路增强 5-氟尿嘧啶对胃腺癌细胞增殖的抑制作用。

β-Ionone enhances the inhibitory effects of 5-fluorouracil on the proliferation of gastric adenocarcinoma cells by the GSK-3β signaling pathway.

机构信息

Department of Clinical Laboratory, The Forth Affiliated Hospital of Harbin Medical University, Nangang District, Harbin, China.

Department of Clinical Laboratory, Xi'an No. 9 Hospital, Beilin District, Xi'an City, China.

出版信息

PLoS One. 2024 Sep 6;19(9):e0309014. doi: 10.1371/journal.pone.0309014. eCollection 2024.

DOI:10.1371/journal.pone.0309014
PMID:39241034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11379261/
Abstract

5-Fluorouracil (5-FU) is widely used in the treatment of gastric cancer, and the emergence of drug resistance and toxic effects has limited its application. Therefore, there is an urgent need for safe and effective novel drugs or new therapies. β-Ionone (BI) is found in vegetables and fruits and possesses an inhibitory proliferation of tumor cells in vitro and in vivo. In this study, we investigated whether BI could enhance the inhibitory effects of 5-FU on the proliferation of gastric adenocarcinoma cells and the growth of gastric cancer cell xenografts in a mouse model. The effects of BI and 5-FU alone or their combination on the cell viability, apoptosis, and mitochondrial membrane potential, the cell cycle, and its related proteins-Cyclin D1, and CDK4 as well as PCNA and GSK-3β were evaluated in SGC-7901 cells and MKN45 cells by MTT, MB, flow cytometry and Western blot. In addition, the effects of BI and 5-FU alone or their combination on the growth of SGC-7901 cell xenografts in nude mice were investigated. The results showed that BI significantly enhanced the sensitivity of gastric adenocarcinoma cells to 5-FU in vitro and in vivo, i.e. proliferation inhibited, apoptosis induced and GSK-3β protein activated. Therefore, our results suggest that BI increases the antitumor effect of 5-FU on gastric adenocarcinoma cells, at least partly from an activated GSK-3β signaling pathway.

摘要

5-氟尿嘧啶(5-FU)被广泛应用于胃癌的治疗,但耐药性和毒副作用的出现限制了其应用。因此,急需安全有效的新型药物或新疗法。β-紫罗兰酮(BI)存在于蔬菜和水果中,具有体外和体内抑制肿瘤细胞增殖的作用。在本研究中,我们研究了 BI 是否可以增强 5-FU 对胃腺癌 SGC-7901 细胞和 MKN45 细胞增殖的抑制作用,以及对荷瘤小鼠胃癌细胞生长的抑制作用。通过 MTT、MB、流式细胞术和 Western blot 检测 BI 和 5-FU 单独或联合作用对 SGC-7901 细胞和 MKN45 细胞活力、凋亡、线粒体膜电位、细胞周期及其相关蛋白-Cyclin D1、CDK4 和 PCNA、GSK-3β的影响。此外,还研究了 BI 和 5-FU 单独或联合作用对裸鼠 SGC-7901 细胞异种移植瘤生长的影响。结果表明,BI 显著增强了胃腺癌细胞对 5-FU 的敏感性,表现为增殖抑制、凋亡诱导和 GSK-3β 蛋白激活。因此,我们的结果表明,BI 增强了 5-FU 对胃腺癌细胞的抗肿瘤作用,至少部分是通过激活 GSK-3β 信号通路实现的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d613/11379261/141b0bedb64e/pone.0309014.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d613/11379261/1f1f579acd54/pone.0309014.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d613/11379261/eb954a6c4ce8/pone.0309014.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d613/11379261/f11dee9dc686/pone.0309014.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d613/11379261/b8370040e17a/pone.0309014.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d613/11379261/31fe2d7b7a80/pone.0309014.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d613/11379261/141b0bedb64e/pone.0309014.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d613/11379261/1f1f579acd54/pone.0309014.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d613/11379261/eb954a6c4ce8/pone.0309014.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d613/11379261/f11dee9dc686/pone.0309014.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d613/11379261/b8370040e17a/pone.0309014.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d613/11379261/31fe2d7b7a80/pone.0309014.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d613/11379261/141b0bedb64e/pone.0309014.g006.jpg

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