The Current Understanding Of Asbestos-Induced Epigenetic Changes Associated With Lung Cancer

被引:23
作者
Cheng, Yuen Yee [1 ,2 ]
Rath, Emma M. [3 ]
Linton, Anthony [1 ,2 ,4 ]
Yuen, Man Lee [1 ]
Takahashi, Ken [1 ]
Lee, Kenneth [1 ,2 ,4 ]
机构
[1] Univ Sydney, Asbestos Dis Res Inst, Sydney Med Sch, Sydney, NSW, Australia
[2] Univ Sydney, Sydney Med Sch, Sydney, NSW, Australia
[3] Garvan Inst Med Res, Sydney, NSW, Australia
[4] Concord Repatriat Gen Hosp, Sydney, NSW, Australia
关键词
lung cancer; epigenetic biomarkers; microRNA; DNA methylation; immunohistochemistry; IHC; fluorescence in situ hybridization; FISH; ABERRANT PROMOTER METHYLATION; SQUAMOUS-CELL CARCINOMA; CPG ISLAND METHYLATION; GROWTH-FACTOR RECEPTOR; DNA METHYLATION; SERUM DNA; CLINICOPATHOLOGICAL SIGNIFICANCE; CROCIDOLITE ASBESTOS; GENOMIC ALTERATIONS; PROGNOSTIC IMPACT;
D O I
10.2147/LCTT.S186843
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 122 条
  • [1] Asbestos causes apoptosis in alveolar epithelial cells: Role of iron-induced free radicals
    Aljandali, A
    Pollack, H
    Yeldandi, A
    Li, YY
    Weitzman, SA
    Kamp, DW
    [J]. JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 2001, 137 (05): : 330 - 339
  • [2] Alvarez J.G.B., 2019, DRUGS CONTEXT, V8
  • [3] American Lung Association, 2019, MES SYMPT CAUS RISK
  • [4] [Anonymous], 2013, World Cancer Report 2014, P1
  • [5] MAP2K1 (MEK1) Mutations Define a Distinct Subset of Lung Adenocarcinoma Associated with Smoking
    Arcila, Maria E.
    Drilon, Alexander
    Sylvester, Brooke E.
    Lovly, Christine M.
    Borsu, Laetitia
    Reva, Boris
    Kris, Mark G.
    Solit, David B.
    Ladanyi, Marc
    [J]. CLINICAL CANCER RESEARCH, 2015, 21 (08) : 1935 - 1943
  • [6] Diagnostic Utility of Genome-wide DNA Methylation Testing in Genetically Unsolved Individuals with Suspected Hereditary Conditions
    Aref-Eshghi, Erfan
    Bend, Eric G.
    Colaiacovo, Samantha
    Caudle, Michelle
    Chakrabarti, Rana
    Napier, Melanie
    Brick, Lauren
    Brady, Lauren
    Carere, Deanna Alexis
    Levy, Michael A.
    Kerkhof, Jennifer
    Stuart, Alan
    Saleh, Maha
    Beaudet, Arthur L.
    Li, Chumei
    Kozenko, Maryia
    Karp, Natalya
    Prasad, Chitra
    Siu, Victoria Mok
    Tarnopolsky, Mark A.
    Ainsworth, Peter J.
    Lin, Hanxin
    Rodenhiser, David I.
    Krantz, Ian D.
    Deardorff, Matthew A.
    Schwartz, Charles E.
    Sadikovic, Bekim
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2019, 104 (04) : 685 - 700
  • [7] Asbestos Safety and Eradication Agency, 2019, ASB
  • [8] Pathways Impacted by Genomic Alterations in Pulmonary Carcinoid Tumors
    Asiedu, Michael K.
    Thomas, Charles F., Jr.
    Dong, Jie
    Schulte, Sandra C.
    Khadka, Prasidda
    Sun, Zhifu
    Kosari, Farhad
    Jen, Jin
    Molina, Julian
    Vasmatzis, George
    Kuang, Ray
    Aubry, Marie Christine
    Yang, Ping
    Wigle, Dennis A.
    [J]. CLINICAL CANCER RESEARCH, 2018, 24 (07) : 1691 - 1704
  • [9] Non-Small Cell Lung Cancer Patients Harboring HER2 Mutations: Clinical Characteristics and Management in a Real-Life Setting. Cohort HER2 EXPLORE GFPC 02-14
    Auliac, Jean-Bernard
    Do, Pascal
    Bayle, Sophie
    Doubre, Helene
    Vinas, Florent
    Letreut, Jacques
    Falchero, Lionel
    Hauss, Pierre Alexandre
    Thomas, Pascal
    Chouaid, Christos
    [J]. ADVANCES IN THERAPY, 2019, 36 (08) : 2161 - 2166
  • [10] Australian Government, LUNG CANC AUSTR STAT