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氢吗啡酮体外抑制人胃癌细胞的抗肿瘤作用。

Antitumor Effects of Hydromorphone on Human Gastric Cancer Cells in vitro.

机构信息

Department of Anesthesiology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, People's Republic of China.

Guangxi Key Laboratory of Enhanced Recovery After Surgery for Gastrointestinal Cancer, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, People's Republic of China.

出版信息

Drug Des Devel Ther. 2023 Apr 6;17:1037-1045. doi: 10.2147/DDDT.S398464. eCollection 2023.

Abstract

INTRODUCTION

Experimental data indicate that morphine and fentanyl may have antitumor effects in gastric cancer cells (GC). Hydromorphone, as an analgesic, is used against refractory cancer pain in recent years. However, the data on hydromorphone influencing the biological characteristics of human gastric cancer cells are lacking. The aim of this study was to investigate how hydromorphone affected the growth of human gastric cancer in vitro.

MATERIAL AND METHODS

Human GC cell lines (HGC-27, MGC-803, AGS and SGC-7901) and human gastric epithelial cells GSE-1 were exposed to various concentrations of hydromorphone (0-800μM). The cell viability, invasion and migration abilities were measured using cell counting kit-8, Transwell and wound healing assays. Apoptosis and cell cycle were evaluated by flow cytometry.

RESULTS

Hydromorphone was toxic in GSE-1 cells at the concentration 800μM. It showed enhanced antitumor effects at a longer incubation time and higher concentrations in HGC-27, MGC-803, AGS and SGC-7901 cells. Hydromorphone inhibited the progression of MGC- 803 cells by cell cycle arrest and apoptosis induction.

CONCLUSION

Hydromorphone suppresses the proliferation of human GC cells in a dose- and time-dependent manner. That may provide a theoretical basis for the clinical application of hydromorphone in the safe and effective treatment of GC.

摘要

简介

实验数据表明,吗啡和芬太尼可能对胃癌细胞(GC)具有抗肿瘤作用。氢吗啡酮作为一种镇痛药,近年来用于治疗难治性癌痛。然而,关于氢吗啡酮影响人胃癌细胞生物学特性的数据尚缺乏。本研究旨在探讨氢吗啡酮如何影响人胃癌在体外的生长。

材料与方法

将人 GC 细胞系(HGC-27、MGC-803、AGS 和 SGC-7901)和人胃上皮细胞 GSE-1 暴露于不同浓度的氢吗啡酮(0-800μM)。通过细胞计数试剂盒-8、Transwell 和划痕愈合实验测量细胞活力、侵袭和迁移能力。通过流式细胞术评估细胞凋亡和细胞周期。

结果

在浓度为 800μM 时,氢吗啡酮对 GSE-1 细胞有毒。在 HGC-27、MGC-803、AGS 和 SGC-7901 细胞中,随着孵育时间的延长和浓度的增加,它表现出增强的抗肿瘤作用。氢吗啡酮通过细胞周期阻滞和诱导细胞凋亡抑制 MGC-803 细胞的进展。

结论

氢吗啡酮以剂量和时间依赖的方式抑制人 GC 细胞的增殖。这可能为临床应用氢吗啡酮安全有效地治疗 GC 提供理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977c/10086391/1ba95c074bb0/DDDT-17-1037-g0001.jpg

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