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实体瘤和血液系统肿瘤中的表观遗传变化。

Epigenetic changes in solid and hematopoietic tumors.

作者信息

Toyota Minoru, Issa Jean-Pierre J

机构信息

Sapporo Medical University, Sapporo, Japan.

出版信息

Semin Oncol. 2005 Oct;32(5):521-30. doi: 10.1053/j.seminoncol.2005.07.003.

Abstract

There are three connected molecular mechanisms of epigenetic cellular memory in mammalian cells: DNA methylation, histone modifications, and RNA interference. The first two have now been firmly linked to neoplastic transformation. Hypermethylation of CpG-rich promoters triggers local histone code modifications resulting in a cellular camouflage mechanism that sequesters gene promoters away from transcription factors and results in stable silencing. This normally restricted mechanism is ubiquitously used in cancer to silence hundreds of genes, among which some critically contribute to the neoplastic phenotype. Virtually every pathway important to cancer formation is affected by this process. Methylation profiling of human cancers reveals tissue-specific epigenetic signatures, as well as tumor-specific signatures, reflecting in particular the presence of epigenetic instability in a subset of cancers affected by the CpG island methylator phenotype. Generally, methylation patterns can be traced to a tissue-specific, proliferation-dependent accumulation of aberrant promoter methylation in aging tissues, a process that can be accelerated by chronic inflammation and less well-defined mechanisms including, possibly, diet and genetic predisposition. The epigenetic machinery can also be altered in cancer by specific lesions in epigenetic effector genes, or by aberrant recruitment of these genes by mutant transcription factors and coactivators. Epigenetic patterns are proving clinically useful in human oncology via risk assessment, early detection, and prognostic classification. Pharmacologic manipulation of these patterns-epigenetic therapy-is also poised to change the way we treat cancer in the clinic.

摘要

在哺乳动物细胞中,存在三种相互关联的表观遗传细胞记忆分子机制:DNA甲基化、组蛋白修饰和RNA干扰。前两种机制现已与肿瘤转化紧密相连。富含CpG的启动子的高甲基化会引发局部组蛋白编码修饰,从而产生一种细胞伪装机制,将基因启动子与转录因子隔离开来,导致稳定的基因沉默。这种通常受到限制的机制在癌症中被广泛用于沉默数百个基因,其中一些基因对肿瘤表型起着关键作用。几乎每一条对癌症形成重要的信号通路都会受到这一过程的影响。人类癌症的甲基化图谱揭示了组织特异性的表观遗传特征以及肿瘤特异性特征,尤其反映了受CpG岛甲基化表型影响的一部分癌症中存在的表观遗传不稳定性。一般来说,甲基化模式可以追溯到衰老组织中异常启动子甲基化的组织特异性、增殖依赖性积累,慢性炎症以及包括饮食和遗传易感性等不太明确机制可能会加速这一过程。表观遗传机制在癌症中也可能因表观遗传效应基因的特定损伤,或因突变转录因子和共激活因子对这些基因的异常招募而发生改变。表观遗传模式在人类肿瘤学中通过风险评估、早期检测和预后分类已被证明具有临床应用价值。对这些模式进行药物调控——表观遗传治疗——也有望改变我们在临床上治疗癌症的方式。

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