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SGC-7901胃癌细胞中植物异喹啉生物碱小檗碱的微小RNA-信使核糖核酸谱整合及通路分析

Integration of microRNA-mRNA profiles and pathway analysis of plant isoquinoline alkaloid berberine in SGC-7901 gastric cancers cells.

作者信息

Yang Yanhong, Zhang Na, Li Kundong, Chen Juan, Qiu Lang, Zhang Jufeng

机构信息

The First Affiliated Hospital, School of Clinical Medicine, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.

School of Life Science and Biopharmacology, Guangdong Pharmaceutical University, Guangzhou Higher Education Mega Center, Guangzhou, People's Republic of China.

出版信息

Drug Des Devel Ther. 2018 Feb 28;12:393-408. doi: 10.2147/DDDT.S155993. eCollection 2018.

Abstract

PURPOSE

Berberine (BBR) is a traditional Chinese medicine normally used for gastroenteritis, and recent research found that it could fight against tumors. In this study, we focused on integrating miRNA sequencing and RNA sequencing of SGC-7901 gastric cancer cells treated by BBR to elucidate their underlying mechanisms.

MATERIALS AND METHODS

WST-1 assay and flow cytometry were used to check the effects of BBR on SGC-7901. miRNA sequencing and RNA sequencing were used to establish the miRNA and mRNA profiles of BBR-treated SGC-7901.

RESULTS

The results showed that BBR could inhibit the proliferation of SGC-7901 cells and induce G1 arrest in cell cycle phase and apoptosis. A total of 1,960 upregulated genes and 4,837 downregulated genes were identified in the RNA sequencing and 347 upregulated and 93 downregulated miRNAs in the miRNA sequencing. A total of 78 novel miRNAs were also found. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analysis showed that the genes were related to pathways in cancer and metabolism. We also analyzed the miRNA-mRNA network of genes grouped into cell cycle, apoptosis, inflammation, metabolism, cell junction, acetylization process, TGF-β pathway, and Wnt signaling pathway.

CONCLUSION

BBR could inhibit the proliferation of SGC-7901 cells and induce apoptosis. Integrated analysis of microRNA-mRNA profiles is a promising approach to validate gene expression patterns associated with malignant phenotype and study the mechanisms of anticancer.

摘要

目的

黄连素(BBR)是一种常用于治疗肠胃炎的传统中药,最近的研究发现它可以对抗肿瘤。在本研究中,我们专注于整合经BBR处理的SGC-7901胃癌细胞的miRNA测序和RNA测序,以阐明其潜在机制。

材料与方法

采用WST-1法和流式细胞术检测BBR对SGC-7901的作用。利用miRNA测序和RNA测序建立经BBR处理的SGC-7901的miRNA和mRNA图谱。

结果

结果表明,BBR可抑制SGC-7901细胞的增殖,诱导细胞周期G1期阻滞和凋亡。RNA测序共鉴定出1960个上调基因和4837个下调基因,miRNA测序共鉴定出347个上调miRNA和93个下调miRNA。还发现了78个新的miRNA。基因本体论和京都基因与基因组百科全书分析表明,这些基因与癌症和代谢途径相关。我们还分析了细胞周期、凋亡、炎症、代谢、细胞连接、乙酰化过程、TGF-β途径和Wnt信号通路中基因的miRNA-mRNA网络。

结论

BBR可抑制SGC-7901细胞的增殖并诱导凋亡。miRNA-mRNA图谱的综合分析是验证与恶性表型相关的基因表达模式和研究抗癌机制的一种有前景的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a07b/5836656/a6e485fa8794/dddt-12-393Fig1.jpg

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