目前对与肺癌相关的石棉诱导表观遗传变化的认识。

IF 5.1 Q1 ONCOLOGY Lung Cancer: Targets and Therapy Pub Date : 2020-01-08 eCollection Date: 2020-01-01 DOI:10.2147/LCTT.S186843
Yuen Yee Cheng, Emma M Rath, Anthony Linton, Man Lee Yuen, Ken Takahashi, Kenneth Lee
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引用次数: 0

摘要

石棉是一种天然矿物,由极其细小的纤维组成,吸入后会滞留在肺部。职业和环境暴露于石棉与肺癌和恶性间皮瘤(一种肺周围内膜的癌症)的发生有关。这篇综述讨论了使石棉诱发肺癌成为一个持续性问题的因素,包括石棉在历史上的广泛使用以及从接触石棉到发病之间长达数十年的潜伏期。对导致肺癌的 DNA 核苷酸基因组突变和基因重排已进行了深入研究,其中一些突变的生物标志物和靶向疗法已用于临床。这些突变生物标志物和靶向疗法所涉及的基因也参与了表观遗传学机制,本综述将对这些基因的表观遗传学畸变进行讨论,希望通过对这些基因畸变的鉴定,能够使用相同的基因生物标志物和靶向疗法。目前,人们对滞留在肺部的石棉纤维如何导致表观遗传变化和肺癌的认识还不全面。研究表明,纤维表面的氧化还原反应会产生活性氧(ROS),进而损伤 DNA,导致基因和表观遗传学改变,降低肿瘤抑制基因的活性。本综述总结了与肺癌有关的表观遗传 DNA 甲基化变化,其中一些变化是由于接触石棉所致。迄今为止,将石棉导致的表观遗传变化与非石棉导致的肺癌表观遗传变化区分开来的研究还很少。与一般肺癌相比,石棉相关肺癌表现出较少的甲基化变异,而且在很大一部分样本中,变异仅限于启动子区域。事实证明,癌症中的表观遗传畸变是很有希望的癌症诊断生物标志物。希望对肺癌表观遗传变化的进一步了解能够产生有用的石棉相关肺癌生物标志物,以指导治疗。利用非侵入性血液和痰液样本检测肺癌表观遗传变化的研究正在进行中。这些努力为未来的无创癌症诊断带来了希望。通过表观遗传疗法逆转肺癌表观遗传畸变的努力正在进行中,但尚未取得成功。
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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The Current Understanding Of Asbestos-Induced Epigenetic Changes Associated With Lung Cancer.

Asbestos is a naturally occurring mineral consisting of extremely fine fibres that can become trapped in the lungs after inhalation. Occupational and environmental exposures to asbestos are linked to development of lung cancer and malignant mesothelioma, a cancer of the lining surrounding the lung. This review discusses the factors that are making asbestos-induced lung cancer a continuing problem, including the extensive historic use of asbestos and decades long latency between exposure and disease development. Genomic mutations of DNA nucleotides and gene rearrangements driving lung cancer are well-studied, with biomarkers and targeted therapies already in clinical use for some of these mutations. The genes involved in these mutation biomarkers and targeted therapies are also involved in epigenetic mechanisms and are discussed in this review as it is hoped that identification of epigenetic aberrations in these genes will enable the same gene biomarkers and targeted therapies to be used. Currently, understanding of how asbestos fibres trapped in the lungs leads to epigenetic changes and lung cancer is incomplete. It has been shown that oxidoreduction reactions on fibre surfaces generate reactive oxygen species (ROS) which in turn damage DNA, leading to genetic and epigenetic alterations that reduce the activity of tumour suppressor genes. Epigenetic DNA methylation changes associated with lung cancer are summarised in this review, and some of these changes will be due to asbestos exposure. So far, little research has been carried out to separate the asbestos driven epigenetic changes from those due to non-asbestos causes of lung cancer. Asbestos-associated lung cancers exhibit less methylation variability than lung cancers in general, and in a large proportion of samples variability has been found to be restricted to promoter regions. Epigenetic aberrations in cancer are proving to be promising biomarkers for diagnosing cancers. It is hoped that further understanding of epigenetic changes in lung cancer can result in useful asbestos-associated lung cancer biomarkers to guide treatment. Research is ongoing into the detection of lung cancer epigenetic alterations using non-invasive samples of blood and sputum. These efforts hold the promise of non-invasive cancer diagnosis in the future. Efforts to reverse epigenetic aberrations in lung cancer by epigenetic therapies are ongoing but have not yet yielded success.

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来源期刊
CiteScore
8.10
自引率
0.00%
发文量
10
审稿时长
16 weeks
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