Epigenetic mechanisms in cancer

Gizem Ors Kumoglu, A. Şendemir, M. B. Tanyolaç, B. Bilir, O. Kucuk, Y. Missirlis
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引用次数: 2

Abstract

: This review aims to give a brief summary of the most common epigenetic mechanisms, and their possible relations with cancer initiation and progression, focusing on the possible physico-chemical factors that might control these epigenetic mechanisms, and giving examples of the epigenetic therapy approaches. Original and review articles encompassing epigenetics and inflammation were screened from major databases including PubMed, Medline, Science Direct, Scopus, etc. in English and analyzed for the writing of this review paper. The importance of epigenetics in linking the effects of environmental factors to changes in gene expression is gaining acceptance more and more in recent years. It is becoming more evident that epigenetics plays an important role in health and disease, cancer being no exception. Although effects of environmental factors on cancer initiation and progression have been known for decades, the exact mechanisms that control these interactions are yet to be discovered. The breakthrough that most epigenetic alterations are reversible brings out a new exciting target for cancer therapeutics. Cancer initiation and progression are controlled by both genetic and epigenetic events. Unlike genetic changes, epigenetic modulations are potentially reversible. Epigenetic drugs that inhibit DNA methylation or histone deacetylation enable reactivation of tumor suppressor genes and suppression of cancer cell growth. Taking advantage of these situations allows the reduction of malignant cell clusters. In addition, clinical results, such as epigenetic drugs targeting specific enzymes for cancer treatment and re-sensitizing cells that do not respond to treatment are promising as cancer therapeutics. To date, numerous epigenetic agents have been developed, several DNA methyltransferase (DNMT) and histone deacetylase (HDAC) inhibitors have been definitively approved by regulatory agencies. Combined multidrug approaches for cancer treatment have overcome the limitations of single-agent epigenetic therapies, increased antitumor effects, and reduced drug resistance. It is evident that as our knowledge on epigenetic mechanisms expand, epigenomics-targeted treatments will become more common in cancer therapy, either as primary therapy or as complementary and alternative treatment options to increase the efficacy of conventional treatments for cancer patients, and epigenetics will maintain its increasing importance for cancer diagnostic, prognostic and therapeutic studies for many years to come. with and these epigenetic approaches. Research published were examined using integrative methodology.
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癌症的表观遗传机制
本文综述了最常见的表观遗传机制及其与癌症发生和发展的可能关系,重点介绍了可能控制这些表观遗传机制的物理化学因素,并举例说明了表观遗传治疗方法。从PubMed、Medline、Science Direct、Scopus等主要英文数据库中筛选涉及表观遗传学和炎症的原创和综述文章,并对其进行分析,以撰写本文。近年来,表观遗传学在将环境因素的影响与基因表达变化联系起来方面的重要性越来越被人们所接受。越来越明显的是,表观遗传学在健康和疾病中起着重要作用,癌症也不例外。虽然环境因素对癌症发生和发展的影响已经知道了几十年,但控制这些相互作用的确切机制尚未被发现。大多数表观遗传改变是可逆的这一突破为癌症治疗带来了一个令人兴奋的新靶点。癌症的发生和发展是由遗传和表观遗传事件控制的。与遗传变化不同,表观遗传调节是潜在可逆的。抑制DNA甲基化或组蛋白去乙酰化的表观遗传药物能够激活肿瘤抑制基因并抑制癌细胞生长。利用这些情况可以减少恶性细胞簇。此外,临床结果表明,针对癌症治疗的特定酶的表观遗传药物和对治疗无反应的细胞再敏化是有希望的癌症治疗方法。迄今为止,许多表观遗传药物已被开发出来,一些DNA甲基转移酶(DNMT)和组蛋白去乙酰化酶(HDAC)抑制剂已被监管机构明确批准。多药联合治疗癌症的方法克服了单药表观遗传治疗的局限性,增加了抗肿瘤效果,减少了耐药性。很明显,随着我们对表观遗传学机制的了解的扩大,表观遗传学靶向治疗将在癌症治疗中变得越来越普遍,无论是作为主要治疗还是作为补充和替代治疗方案,以提高癌症患者常规治疗的疗效,表观遗传学在癌症诊断、预后和治疗研究中仍将保持其日益重要的地位。用这些表观遗传方法。发表的研究采用综合方法进行检查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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