Li Chun-Qing, Liu Zhi-Qin, Liu Sha-Sha, Zhang Gao-Tao, Jiang Li, Chen Chuan, Luo Du-Qiang
Key Laboratory of Microbial Diversity Research and Application of Hebei Province, College of Life Science, Hebei University, Baoding, China.
Key Laboratory of Pharmaceutical Quality Control of Hebei Province, College of Pharmaceutical Science, Hebei University, Baoding, China.
Front Pharmacol. 2022 Mar 23;13:822023. doi: 10.3389/fphar.2022.822023. eCollection 2022.
Metformin is a kind of widely used antidiabetic drug that regulates glucose homeostasis by inhibiting liver glucose production and increasing muscle glucose uptake. Recently, some studies showed that metformin exhibits anticancer properties in a variety of cancers. Although several antitumor mechanisms have been proposed for metformin action, its mode of action in human liver cancer remains not elucidated. In our study, we investigated the underlying molecular mechanisms of metformin's antitumor effect on Huh-7 cells of hepatocellular carcinoma (HCC) . RNA sequencing was performed to explore the effect of metformin on the transcriptome of Huh-7 cells. The results revealed that 4,518 genes (with log2 fold change > 1 or < -1, adjusted p-value < 0.05) were differentially expressed in Huh-7 cells with treatment of 25-mM metformin compared with 0-mM metformin, including 1,812 upregulated and 2,706 downregulated genes. Gene ontology and Kyoto Encyclopedia of Genes and Genomes pathway analyses identified 54 classical pathways that were significantly enriched, and 16 pathways are closely associated with cancer, such as cell cycle, DNA replication, extracellular matrix-receptor interaction, and so on. We selected 11 differentially expressed genes, which are closely associated with HCC, to validate their differential expressions through a quantitative real-time reverse transcription-polymerase chain reaction. The result exhibited that the genes of fatty acid synthase, mini-chromosome maintenance complex components 6 and 5, myristoylated alanine-rich C-kinase substrate, fatty acid desaturase 2, C-X-C motif chemokine ligand 1, bone morphogenetic protein 4, S-phase kinase-associated protein 2, kininogen 1, and proliferating cell nuclear antigen were downregulated, and Dual-specificity phosphatase-1 is significantly upregulated in Huh-7 cells with treatment of 25-mM metformin. These differentially expressed genes and pathways might play a crucial part in the antitumor effect of metformin and might be potential targets of metformin treating HCC. Further investigations are required to evaluate the metformin mechanisms of anticancer action .
二甲双胍是一种广泛使用的抗糖尿病药物,它通过抑制肝脏葡萄糖生成和增加肌肉葡萄糖摄取来调节葡萄糖稳态。最近,一些研究表明二甲双胍在多种癌症中具有抗癌特性。尽管已经提出了几种二甲双胍作用的抗肿瘤机制,但其在人类肝癌中的作用模式仍未阐明。在我们的研究中,我们调查了二甲双胍对肝癌(HCC)Huh-7细胞抗肿瘤作用的潜在分子机制。进行RNA测序以探索二甲双胍对Huh-7细胞转录组的影响。结果显示,与0 mM二甲双胍处理的Huh-7细胞相比,25 mM二甲双胍处理的Huh-7细胞中有4518个基因(log2倍数变化>1或<-1,校正p值<0.05)差异表达,其中包括1812个上调基因和2706个下调基因。基因本体论和京都基因与基因组百科全书通路分析确定了54条显著富集的经典通路,其中16条通路与癌症密切相关,如细胞周期、DNA复制、细胞外基质-受体相互作用等。我们选择了11个与HCC密切相关的差异表达基因,通过定量实时逆转录-聚合酶链反应验证它们的差异表达。结果表明,脂肪酸合酶、微型染色体维持复合体成分6和5、富含肉豆蔻酰化丙氨酸的C激酶底物、脂肪酸去饱和酶2、C-X-C基序趋化因子配体1、骨形态发生蛋白4、S期激酶相关蛋白2、激肽原1和增殖细胞核抗原在25 mM二甲双胍处理的Huh-7细胞中下调,而双特异性磷酸酶-1显著上调。这些差异表达的基因和通路可能在二甲双胍的抗肿瘤作用中起关键作用,可能是二甲双胍治疗HCC的潜在靶点。需要进一步研究来评估二甲双胍的抗癌作用机制。