Cinnamomi ramulus inhibits cancer cells growth by inducing G2/M arrest

被引:6
作者
Li, Jing [1 ,2 ]
Huang, Hsi-Yuan [1 ,2 ]
Lin, Yang-Chi-Dung [1 ,2 ]
Zuo, Huali [1 ,2 ]
Tang, Yun [1 ,2 ]
Huang, Hsien-Da [1 ,2 ]
机构
[1] Chinese Univ Hong Kong, Sch Med, Shenzhen, Guangdong, Peoples R China
[2] Chinese Univ Hong Kong, Warshel Inst Computat Biol, Shenzhen, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Cinnamomi ramulus; transcriptomic analysis; differential expression analysis (DE); gene set enrichment analysis (GSEA); cell cycle; WEB SERVER; CYCLE;
D O I
10.3389/fphar.2023.1121799
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Cinnamomi ramulus (CR) is one of the most widely used traditional Chinese medicine (TCM) with anti-cancer effects. Analyzing transcriptomic responses of different human cell lines to TCM treatment is a promising approach to understand the unbiased mechanism of TCM. Methods: This study treated ten cancer cell lines with different CR concentrations, followed by mRNA sequencing. Differential expression (DE) analysis and gene set enrichment analysis (GSEA) were utilized to analyze transcriptomic data. Finally, the in silico screening results were verified by in vitro experiments. Results: Both DE and GSEA analysis suggested the Cell cycle pathway was the most perturbated pathway by CR across these cell lines. By analyzing the clinical significance and prognosis of G2/M related genes (PLK1, CDK1, CCNB1, and CCNB2) in various cancer tissues, we found that they were up-regulated in most cancer types, and their down-regulation showed better overall survival rates in cancer patients. Finally, in vitro experiments validation on A549, Hep G2, and HeLa cells suggested that CR can inhibit cell growth by suppressing the PLK1/CDK1/ Cyclin B axis. Discussion: This is the first study to apply transcriptomic analysis to investigate the cancer cell growth inhibition of CR on various human cancer cell lines. The core effect of CR on ten cancer cell lines is to induce G2/M arrest by inhibiting the PLK1/CDK1/Cyclin B axis.
引用
收藏
页数:15
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