Gao Lei, Du Fengying, Wang Jinshen, Zhao Yuhua, Liu Junhua, Cai Da, Zhang Xiao, Wang Yutao, Zhang Shuqiu
Institute of Quality Standard and Testing Technology for Agro-Products, Shandong Academy of Agricultural Sciences, Jinan, Shandong 250100, P.R. China.
Shandong Provincial Key Laboratory of Test Technology on Food Quality and Safety, Jinan, Shandong 250100, P.R. China.
Oncol Lett. 2021 Oct;22(4):690. doi: 10.3892/ol.2021.12951. Epub 2021 Aug 1.
Sulforaphane and sulforaphene are isothiocyanate compounds derived from cruciferous vegetables that have demonstrated antiproliferative properties against colon cancer. However, the underlying mechanism of action of these two compounds has yet to be elucidated. The aim of the present study was to examine the effects of sulforaphane and sulforaphene on colon cancer using next-generation sequencing (NGS). The SW480 colon cancer cell line was cultured with 25 µmol/l sulforaphane or sulforaphene. Total RNA was extracted from the cells following 48 h of incubation with these compounds, and NGS was performed. Pearson's correlation and principal component analyses were performed on the NGS data in order to determine sample homogeneity followed by hierarchical clustering, chromosomal location, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses. A total of 873 probes in the sulforaphene group were differentially expressed compared with the control group. Similarly, 959 probes in the sulforaphane group were differentially expressed compared with the control group. The differentially expressed genes were dispersed on the chromosomes, across 22 pairs of autosomes, as well as the X and Y chromosomes. GO and KEGG analyses demonstrated that both drugs affected the 'p53 signaling pathway', 'MAPK signaling pathway', 'FOXO signaling pathway' and 'estrogen signaling pathway', while 'Wnt signaling pathway' was enriched in the sulforaphane group, and 'ubiquitin mediated proteolysis' and 'estrogen signaling pathway' in the sulforaphene group. Thus, sulforaphane and sulforaphene exhibited similar biological activities on colon cancer cells. Sulforaphane and sulforaphene may be associated with Wnt and estrogen signaling, respectively.
萝卜硫素和萝卜硫酚是源自十字花科蔬菜的异硫氰酸酯化合物,已证明它们对结肠癌具有抗增殖特性。然而,这两种化合物的潜在作用机制尚未阐明。本研究的目的是使用下一代测序(NGS)来研究萝卜硫素和萝卜硫酚对结肠癌的影响。将SW480结肠癌细胞系用25μmol/l的萝卜硫素或萝卜硫酚培养。在用这些化合物孵育48小时后从细胞中提取总RNA,并进行NGS。对NGS数据进行Pearson相关性分析和主成分分析,以确定样本同质性,随后进行层次聚类、染色体定位、基因本体(GO)和京都基因与基因组百科全书(KEGG)通路富集分析。与对照组相比,萝卜硫酚组共有873个探针差异表达。同样,与对照组相比,萝卜硫素组有959个探针差异表达。差异表达基因分散在染色体上,分布于22对常染色体以及X和Y染色体上。GO和KEGG分析表明,两种药物均影响“p53信号通路”、“MAPK信号通路”、“FOXO信号通路”和“雌激素信号通路”,而“Wnt信号通路”在萝卜硫素组中富集,“泛素介导的蛋白水解”和“雌激素信号通路”在萝卜硫酚组中富集。因此,萝卜硫素和萝卜硫酚对结肠癌细胞表现出相似的生物学活性。萝卜硫素和萝卜硫酚可能分别与Wnt和雌激素信号传导有关。