Targeted nutrigenomics as a means of breast cancer management: from DNA methylation to microRNAs

R. Hashemi, S. Arefhosseini, G. Folkerts, S. Varasteh, M. Morshedi
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Abstract

Breast Cancer (BC) is the most prevalent cancer affecting females and the leading cause of death around the world. The World Health Organization (WHO) has announced that the incidence of BC increases approximately 1.8-2 % annually. Hence, it is important that new prevention and treatment strategies involving epigenetics and nutrigenomics are explored. Epigenetics refers to potential changes in gene expression and chromatin structure without alteration of DNA sequence, but still modulates the expression of a particular phenotype. Nutrigenomics determines the effect of dietary habits on cancer risk and tumor behavior, both in progression and inhibition of cancer. The modulation of chromatin structure is an essential component in the regulation of transcriptional activation and repression. Therefore, identifying the regulators of gene expression changes during cancer progression is essential for early diagnosis and inhibition of this malignancy. The methylation of promoter genes, as well as the interplay between microRNAs (miRNAs) and messenger RNAs (mRNAs) of target genes, is the primary component of epigenetics. Any defect in these processes is considered a crucial mechanism for gene and pathway dysregulation in all human cancers, including BC. Nutritional genomic and epigenetic mechanisms may play a pivotal role in prevention as well as early diagnosis of BC, especially for closely related female family members of BC patients. It seems cytosine methylation in Cytosine-phosphate-Guanine dinucleotide (CpG) Islands reflects changes in balance tissues rigidity. Hypo- and hypermethylation of CpG Islands (CGIs) play a crucial role in development of BC via up-regulation of oncogenes and down-regulation of tumor suppressor genes (TSGs). These could be the most effective mechanisms to distinguish BC from other types of cancer. beneficial effects of some nutritional components on the function and structure of non-coding RNA and DNA methylation. We also discuss the role of nutrigenomics as a non-invasive method to explore the epigenetic mechanisms involved in BC and also in the prevention, treatment, early diagnosis, and distinguishing a variety of cancers from each other. In addition, the importance of non-coding RNAs, including miRNAs in body fluids, also need to be further clarified.
靶向营养基因组学作为乳腺癌管理的一种手段:从DNA甲基化到microrna
乳腺癌(BC)是影响女性的最普遍的癌症,也是世界上导致死亡的主要原因。世界卫生组织(WHO)宣布,BC的发病率每年增加约1.8- 2%。因此,探索涉及表观遗传学和营养基因组学的新的预防和治疗策略是很重要的。表观遗传学是指基因表达和染色质结构的潜在变化而不改变DNA序列,但仍然调节特定表型的表达。营养基因组学确定了饮食习惯对癌症风险和肿瘤行为的影响,包括癌症的进展和抑制。染色质结构的调节是调控转录激活和抑制的重要组成部分。因此,确定癌症进展过程中基因表达变化的调节因子对于早期诊断和抑制这种恶性肿瘤至关重要。启动子基因的甲基化以及靶基因的microRNAs (miRNAs)和信使rna (mrna)之间的相互作用是表观遗传学的主要组成部分。这些过程中的任何缺陷都被认为是所有人类癌症(包括BC)中基因和通路失调的关键机制。营养基因组和表观遗传机制可能在BC的预防和早期诊断中发挥关键作用,特别是对BC患者的近亲属女性家庭成员。胞嘧啶-磷酸-鸟嘌呤二核苷酸(CpG)岛胞嘧啶甲基化反映了平衡组织刚性的变化。CpG岛的低甲基化和高甲基化通过上调癌基因和下调肿瘤抑制基因(TSGs)在BC的发展中起着至关重要的作用。这些可能是区分BC和其他类型癌症最有效的机制。一些营养成分对非编码RNA和DNA甲基化功能和结构的有益影响。我们还讨论了营养基因组学作为一种非侵入性方法的作用,以探索BC的表观遗传机制,以及在预防、治疗、早期诊断和区分各种癌症方面的作用。此外,包括体液中的mirna在内的非编码rna的重要性也需要进一步明确。
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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