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一项关于在 NSCLC 中解锁表观遗传学潜力的进展的系统评价:最新进展和展望。

A Systematic Review of Progress toward Unlocking the Power of Epigenetics in NSCLC: Latest Updates and Perspectives.

机构信息

Department of Clinical Molecular Biology, Medical University of Bialystok, 15-269 Bialystok, Poland.

Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.

出版信息

Cells. 2023 Mar 15;12(6):905. doi: 10.3390/cells12060905.

Abstract

Epigenetic research has the potential to improve our understanding of the pathogenesis of cancer, specifically non-small-cell lung cancer, and support our efforts to personalize the management of the disease. Epigenetic alterations are expected to have relevance for early detection, diagnosis, outcome prediction, and tumor response to therapy. Additionally, epi-drugs as therapeutic modalities may lead to the recovery of genes delaying tumor growth, thus increasing survival rates, and may be effective against tumors without druggable mutations. Epigenetic changes involve DNA methylation, histone modifications, and the activity of non-coding RNAs, causing gene expression changes and their mutual interactions. This systematic review, based on 110 studies, gives a comprehensive overview of new perspectives on diagnostic (28 studies) and prognostic (25 studies) epigenetic biomarkers, as well as epigenetic treatment options (57 studies) for non-small-cell lung cancer. This paper outlines the crosstalk between epigenetic and genetic factors as well as elucidates clinical contexts including epigenetic treatments, such as dietary supplements and food additives, which serve as anti-carcinogenic compounds and regulators of cellular epigenetics and which are used to reduce toxicity. Furthermore, a future-oriented exploration of epigenetic studies in NSCLC is presented. The findings suggest that additional studies are necessary to comprehend the mechanisms of epigenetic changes and investigate biomarkers, response rates, and tailored combinations of treatments. In the future, epigenetics could have the potential to become an integral part of diagnostics, prognostics, and personalized treatment in NSCLC.

摘要

表观遗传学研究有可能增进我们对癌症发病机制的理解,特别是非小细胞肺癌,并支持我们努力实现疾病的个体化管理。表观遗传改变有望与早期检测、诊断、预后预测以及肿瘤对治疗的反应相关。此外,作为治疗手段的表观遗传学药物可能会导致延迟肿瘤生长的基因恢复,从而提高生存率,并且可能对没有可用药突变的肿瘤有效。表观遗传变化涉及 DNA 甲基化、组蛋白修饰和非编码 RNA 的活性,导致基因表达变化及其相互作用。基于 110 项研究的这项系统评价全面概述了非小细胞肺癌诊断(28 项研究)和预后(25 项研究)的表观遗传生物标志物以及表观遗传治疗选择(57 项研究)的新观点。本文概述了表观遗传和遗传因素之间的相互作用,并阐明了包括饮食补充剂和食品添加剂等表观遗传治疗在内的临床背景,这些补充剂和添加剂是作为抗癌化合物和细胞表观遗传调节剂,用于降低毒性。此外,还对非小细胞肺癌中的表观遗传学研究进行了前瞻性探索。研究结果表明,需要进一步研究以了解表观遗传变化的机制,并研究生物标志物、反应率以及个体化治疗的联合应用。将来,表观遗传学有可能成为非小细胞肺癌诊断、预后和个体化治疗的一个组成部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70c2/10047383/3c6cbbab9b42/cells-12-00905-g001.jpg

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