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有机硫化合物对癌症的前瞻性表观遗传作用:前景与分子机制

Prospective Epigenetic Actions of Organo-Sulfur Compounds against Cancer: Perspectives and Molecular Mechanisms.

作者信息

Shoaib Shoaib, Ansari Mohammad Azam, Ghazwani Mohammed, Hani Umme, Jamous Yahya F, Alali Zahraa, Wahab Shadma, Ahmad Wasim, Weir Sydney A, Alomary Mohammad N, Yusuf Nabiha, Islam Najmul

机构信息

Department of Biochemistry, Faculty of Medicine, Aligarh Muslim University, Aligarh 202001, Uttar Pradesh, India.

Department of Epidemic Disease Research, Institute for Research and Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, Dammam 31441, Saudi Arabia.

出版信息

Cancers (Basel). 2023 Jan 23;15(3):697. doi: 10.3390/cancers15030697.

Abstract

Major epigenetic alterations, such as chromatin modifications, DNA methylation, and miRNA regulation, have gained greater attention and play significant roles in oncogenesis, representing a new paradigm in our understanding of cancer susceptibility. These epigenetic changes, particularly aberrant promoter hypermethylation, abnormal histone acetylation, and miRNA dysregulation, represent a set of epigenetic patterns that contribute to inappropriate gene silencing at every stage of cancer progression. Notably, the cancer epigenome possesses various HDACs and DNMTs, which participate in the histone modifications and DNA methylation. As a result, there is an unmet need for developing the epigenetic inhibitors against HDACs and DNMTs for cancer therapy. To date, several epigenetically active synthetic inhibitors of DNA methyltransferases and histone deacetylases have been developed. However, a growing body of research reports that most of these synthetic inhibitors have significant side effects and a narrow window of specificity for cancer cells. Targeting tumor epigenetics with phytocompounds that have the capacity to modulate abnormal DNA methylation, histone acetylation, and miRNAs expression is one of the evolving strategies for cancer prevention. Encouragingly, there are many bioactive phytochemicals, including organo-sulfur compounds that have been shown to alter the expression of key tumor suppressor genes, oncogenes, and oncogenic miRNAs through modulation of DNA methylation and histones in cancer. In addition to vitamins and microelements, dietary phytochemicals such as sulforaphane, PEITC, BITC, DADS, and allicin are among a growing list of naturally occurring anticancer agents that have been studied as an alternative strategy for cancer treatment and prevention. Moreover, these bioactive organo-sulfur compounds, either alone or in combination with other standard cancer drugs or phytochemicals, showed promising results against many cancers. Here, we particularly summarize and focus on the impact of specific organo-sulfur compounds on DNA methylation and histone modifications through targeting the expression of different DNMTs and HDACs that are of particular interest in cancer therapy and prevention.

摘要

主要的表观遗传改变,如染色质修饰、DNA甲基化和miRNA调控,已受到更多关注,并在肿瘤发生过程中发挥重要作用,代表了我们对癌症易感性理解的新范式。这些表观遗传变化,特别是异常的启动子高甲基化、异常的组蛋白乙酰化和miRNA失调,代表了一组表观遗传模式,它们在癌症进展的每个阶段都导致不适当的基因沉默。值得注意的是,癌症表观基因组拥有多种HDAC和DNMT,它们参与组蛋白修饰和DNA甲基化。因此,开发针对HDAC和DNMT的表观遗传抑制剂用于癌症治疗的需求尚未得到满足。迄今为止,已经开发了几种具有表观遗传活性的DNA甲基转移酶和组蛋白脱乙酰酶合成抑制剂。然而,越来越多的研究报告称,这些合成抑制剂中的大多数具有显著的副作用,并且对癌细胞的特异性窗口较窄。用能够调节异常DNA甲基化、组蛋白乙酰化和miRNA表达的植物化合物靶向肿瘤表观遗传学是癌症预防的一种不断发展的策略。令人鼓舞的是,有许多生物活性植物化学物质,包括有机硫化合物,已被证明可通过调节癌症中的DNA甲基化和组蛋白来改变关键肿瘤抑制基因、癌基因和致癌miRNA的表达。除了维生素和微量元素外,膳食植物化学物质如萝卜硫素、PEITC、BITC、DADS和大蒜素是越来越多的天然抗癌剂之一,它们已被研究作为癌症治疗和预防的替代策略。此外,这些生物活性有机硫化合物单独或与其他标准癌症药物或植物化学物质联合使用,对许多癌症都显示出有希望的结果。在这里,我们特别总结并关注特定有机硫化合物通过靶向对癌症治疗和预防特别感兴趣的不同DNMT和HDAC的表达对DNA甲基化和组蛋白修饰的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39c2/9913804/edfdcaf8a426/cancers-15-00697-g001.jpg

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