摘要
表观遗传修饰在可逆的,稳定的和基因型独立的方式中决定表型特征。表观遗传修饰主要包括CpG岛的甲基化和组蛋白修饰,都是重要的恶性肿瘤的发病机制。表观遗传现象的可逆性提供了合适的治疗方案,即表观遗传沉默的肿瘤抑制基因的激活。DNA甲基转移酶抑制剂,组蛋白去乙酰化酶和Aurora B kinase单独地或共同地能切实预防或逆转的表观遗传沉默的影响。MicroRNAs [miRNAs] 是表观基因表达调控的一个重要层面,并作为诊断和预后的生物标志物以及许多类型癌症的治疗目标。miRNA参与基因沉默或基因的激活、抑癌基因和癌基因,他们的调制为设计新的癌症治疗剂开辟了新的视野。
关键词: 肿瘤表观遗传学,DNA甲基化酶抑制剂,Epi-药物,Epi-miRs
Current Cancer Drug Targets
Title:Epi-Drugs and Epi-miRs: Moving Beyond Current Cancer Therapies
Volume: 16 Issue: 9
Author(s): Reza Salarinia, Amirhossein Sahebkar, Mostafa Peyvandi, Hamid Reza Mirzaei, Mahmoud Reza Jaafari, Maryam Matbou Riahi and Hamed Ebrahimnejad, Javid Sadri Nahand, Jamshid Hadjati, Mobina Ostadi Asrami, Sara Fadaei, Rasoul Salehi, Hamed Mirzaei
Affiliation:
关键词: 肿瘤表观遗传学,DNA甲基化酶抑制剂,Epi-药物,Epi-miRs
摘要: Epigenetic modifications determine phenotypic characteristics in a reversible, stable and genotype-independent manner. Epigenetic modifications mainly encompass CpG island methylation and histone modifications, both being important in the pathogenesis of malignancies. The reversibility of epigenetic phenomenon provides a suitable therapeutic option that is reactivation of epigenetically silenced tumor-suppressor genes. Inhibition of DNA methyltransferase, histone deacetylase and Aurora B kinase, individually or collectively, could feasibly prevent or reverse the impact of epigenetic silencing. MicroRNAs [miRNAs] are an important layer of epigenetic controlling of gene expression, and serve as diagnostic and prognostic biomarkers as well as treatment targets for several types of cancer. miRNAs are involved inepigenetically silencing or activation of genes, tumor suppressor genes and oncogenes, and their modulation opens new horizons for designing novel cancer therapeutic agents.
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Reza Salarinia, Amirhossein Sahebkar, Mostafa Peyvandi, Hamid Reza Mirzaei, Mahmoud Reza Jaafari, Maryam Matbou Riahi and Hamed Ebrahimnejad, Javid Sadri Nahand, Jamshid Hadjati, Mobina Ostadi Asrami, Sara Fadaei, Rasoul Salehi, Hamed Mirzaei , Epi-Drugs and Epi-miRs: Moving Beyond Current Cancer Therapies, Current Cancer Drug Targets 2016; 16 (9) . https://dx.doi.org/10.2174/1568009616666151207110143
DOI https://dx.doi.org/10.2174/1568009616666151207110143 |
Print ISSN 1568-0096 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5576 |
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