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首页> 外文期刊>Journal of cellular and molecular medicine. >Epigenetic reprogramming of human lung cancer cells with the extract of bovine parthenogenetic oocytes
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Epigenetic reprogramming of human lung cancer cells with the extract of bovine parthenogenetic oocytes

机译:牛孤雌生殖卵母细胞提取物对人肺癌细胞进行表观遗传重编程

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AbstractThe tumour suppressor gene silencing and proto-oncogene activation caused by epigenetic alterations plays an important role in the initiation and progression of cancer. Re-establishing the balance between the expression of tumour suppressor genes and proto-oncogenes by epigenetic modulation is a promising strategy for cancer treatment. In this study, we investigated whether cancer cells can be epigenetically reprogrammed by oocyte extract. H460 human lung cancer cells were reversibly permeabilized and incubated with the extract of bovine parthenogenetic oocytes. Bisulphite sequencing showed that bovine parthenogenetic oocyte extract induced significant demethylation at the promoters of the tumour suppressor genes RUNX3 and CDH1, but not at the promoter of the oncogenic pluripotency gene SOX2. Chromatin immunoprecipitation showed that the histone modifications at RUNX3 and CDH1 promoters were modulated towards a transcriptionally activating state, while those at SOX2 promoter towards a transcriptionally repressive state. Correspondingly, bovine parthenogenetic oocyte extract reversed the epigenetic silencing of RUNX3 and CDH1, and repressed the expression of SOX2. At the functional level, proliferation, anchorage-independent growth, migration and invasion of H460 cells was strongly inhibited. These results indicate that bovine parthenogenetic oocyte extract changes the expression patterns of tumour suppressor and oncogenic genes in cancer cells by remodelling the epigenetic modifications at their promoters. Bovine parthenogenetic oocyte extract may provide a useful tool for epigenetically reprogramming cancer cells and for dissecting the epigenetic mechanisms involved in tumorigenesis.
机译:摘要表观遗传改变引起的抑癌基因沉默和原癌基因激活在癌症的发生和发展中起着重要作用。通过表观遗传调节在肿瘤抑制基因和原癌基因的表达之间重新建立平衡是一种有前途的癌症治疗策略。在这项研究中,我们研究了是否可以通过卵母细胞提取物对表观遗传学上的癌细胞进行重编程。 H460人肺癌细胞可逆渗透,并与牛孤雌卵母细胞提取物一起孵育。亚硫酸氢盐测序表明,牛孤雌卵母细胞提取物在抑癌基因RUNX3和CDH1的启动子处诱导了显着的去甲基化作用,而在致癌多能性基因SOX2的启动子处却没有诱导该作用。染色质免疫沉淀表明,RUNX3和CDH1启动子上的组蛋白修饰被调节成转录激活状态,而SOX2启动子上的组蛋白修饰被调节成转录抑制状态。相应地,牛孤雌卵母细胞提取物逆转了RUNX3和CDH1的表观遗传沉默,并抑制了SOX2的表达。在功能水平上,H460细胞的增殖,独立于锚定的生长,迁移和侵袭均受到强烈抑制。这些结果表明,牛孤雌性卵母细胞提取物通过重构其启动子的表观遗传修饰来改变癌细胞中肿瘤抑制基因和致癌基因的表达模式。牛孤雌卵母细胞提取物可能为表观遗传学重编程癌细胞和解剖涉及肿瘤发生的表观遗传机制提供有用的工具。

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