Epigenetic paradigm of DNA methylation for understanding the pathophysiology, diagnostics, and therapeutics in sarcomas.

IF 2.6 4区 医学 Q2 GENETICS & HEREDITY
Sujata Bhattacharya, Harshita Makkar, Jagdish Prasad Meena, Aditya Kumar Gupta, Rachna Seth
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引用次数: 0

Abstract

Sarcomas are heterogeneous malignant tumors originating from mesenchymal tissues, presenting substantial diagnostic and therapeutic challenges. The diverse genetic and epigenetic landscape provides significant heterogeneity and complexity to the disease, ultimately leading to poor outcomes for affected individuals, especially in metastatic diseases. As research in this field evolves, incorporating methylation profiling into routine clinical practice could significantly enhance the early diagnosis, risk stratification, and personalized treatment strategies for sarcoma patients. Moreover, the integration of advanced genetic techniques and ongoing upgradation in treatment strategies, predominantly those targeting methylation modifications, may lead to improved survival outcomes in sarcomas. We conducted a structured literature review using PubMed, Scopus, Embase, Google Scholar, and Web of Science, encompassing publications up to 30 November 2024. The search focused on DNA methylation in sarcoma pathogenesis, diagnostics, and therapeutics. Relevant articles were screened, and key findings were synthesized thematically. In this review, we provide a comprehensive insight into the role of DNA methylation in promoting sarcomas. We emphasize subtype-associated methylation patterns in sarcomas and their value as prognostic and diagnostic biomarkers, revealing their synergistic effects with the existing treatment regimens. Despite having preclinical outcomes, the translation of these therapies into clinical practice remains a challenge.

DNA甲基化的表观遗传学范式,用于理解肉瘤的病理生理、诊断和治疗。
肉瘤是起源于间质组织的异质性恶性肿瘤,对诊断和治疗提出了重大挑战。不同的遗传和表观遗传景观为疾病提供了显著的异质性和复杂性,最终导致受影响个体的预后不良,特别是在转移性疾病中。随着该领域研究的发展,将甲基化分析纳入常规临床实践可以显著提高肉瘤患者的早期诊断、风险分层和个性化治疗策略。此外,先进的基因技术的整合和治疗策略的持续升级,主要是针对甲基化修饰的治疗策略,可能会改善肉瘤的生存结果。我们使用PubMed、Scopus、Embase、b谷歌Scholar和Web of Science进行了结构化的文献综述,包括截至2024年11月30日的出版物。研究的重点是DNA甲基化在肉瘤发病机制、诊断和治疗中的作用。对相关文章进行筛选,并对主要发现进行专题综合。在这篇综述中,我们提供了一个全面的洞察DNA甲基化在促进肉瘤中的作用。我们强调肉瘤中亚型相关的甲基化模式及其作为预后和诊断生物标志物的价值,揭示它们与现有治疗方案的协同作用。尽管有临床前结果,将这些疗法转化为临床实践仍然是一个挑战。
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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来源期刊
Epigenomics
Epigenomics GENETICS & HEREDITY-
CiteScore
5.80
自引率
2.60%
发文量
95
审稿时长
>12 weeks
期刊介绍: Epigenomics provides the forum to address the rapidly progressing research developments in this ever-expanding field; to report on the major challenges ahead and critical advances that are propelling the science forward. The journal delivers this information in concise, at-a-glance article formats – invaluable to a time constrained community. Substantial developments in our current knowledge and understanding of genomics and epigenetics are constantly being made, yet this field is still in its infancy. Epigenomics provides a critical overview of the latest and most significant advances as they unfold and explores their potential application in the clinical setting.
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