Afroze Nazia, Haque Shafiul, Hussain Arif
School of Life Sciences, Manipal Academy of Higher Education, Dubai, UAE.
Department of Nursing, College of Nursing and Health Sciences, Jazan University, Jazan, Saudi Arabia.
J Cell Mol Med. 2025 Apr;29(7):e70498. doi: 10.1111/jcmm.70498.
Dietary bioactive agents can curb tumour progression through chromatin alterations. Thus, this study attempts to evaluate the influence of kaempferol on epigenome modification in HeLa cells. Biochemical analysis for global DNA methylation-LINE 1, DNMTs (DNA methyltransferases), HAT (histone acetyl transferase), HDACs (histone deacetylases) and HMTs (histone methyltransferases) were examined with their transcript level expression through qPCR. Also, H3 and H4 histone modification marks were quantitated by an ELISA-based assay. Moreover, qPCR and protein profiler were performed to analyse the expression of migratory genes at both mRNA and protein levels, respectively, that was further substantiated through colony formation, invasion, and scratch wound assays. Finally, DNA methyl-sequencing was performed to analyse the promoter methylation of TSGs (tumour suppressor genes) and corroborated by analysing selected TSGs' expression. Kaempferol treatment did not alter the global DNA methylation-LINE 1 compared to untreated control, however, it reduced the expression and biochemical activities of DNMT and HDAC, which can be linked to their hypermethylation by kaempferol exposure. Concordant with the reduced expression of HMTs, HATs and other epi-enzymes, various histone H3 and H4 marks were also observed to be modulated. Kaempferol exposure led to promoter hypomethylation of various TSGs (such as WIF1, RUNX1, RARβ, SOX1), which subsequently led to enhanced expression at the mRNA level, which corresponds to their reactivation. Molecular studies were consistent with cell-based studies, which demonstrated a strong growth inhibitory and anti-migratory effect of kaempferol. This research helps to understand the probable mechanism used by kaempferol as a potential epigenetic modifier.
膳食生物活性物质可通过染色质改变抑制肿瘤进展。因此,本研究试图评估山奈酚对HeLa细胞表观基因组修饰的影响。通过qPCR检测了1号长散在核元件(LINE 1)的整体DNA甲基化、DNA甲基转移酶(DNMTs)、组蛋白乙酰转移酶(HAT)、组蛋白去乙酰化酶(HDACs)和组蛋白甲基转移酶(HMTs)的生化分析及其转录水平表达。此外,通过基于酶联免疫吸附测定(ELISA)的方法对H3和H4组蛋白修饰标记进行了定量。此外,分别通过qPCR和蛋白质分析器分析了迁移基因在mRNA和蛋白质水平的表达,并通过集落形成、侵袭和划痕试验进一步证实。最后,进行了DNA甲基化测序以分析肿瘤抑制基因(TSGs)的启动子甲基化,并通过分析选定TSGs的表达进行了确证。与未处理的对照相比,山奈酚处理未改变1号长散在核元件的整体DNA甲基化,然而,它降低了DNMT和HDAC的表达及生化活性,这可能与其因山奈酚暴露导致的高甲基化有关。与HMTs、HATs和其他表观酶表达降低一致,还观察到各种组蛋白H3和H4标记受到调节。山奈酚暴露导致各种TSGs(如WIF1、RUNX1、RARβ、SOX1)的启动子低甲基化,随后导致mRNA水平表达增强,这与其重新激活相对应。分子研究与基于细胞的研究一致,后者证明了山奈酚具有强大的生长抑制和抗迁移作用。这项研究有助于理解山奈酚作为潜在表观遗传修饰剂所使用的可能机制。