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恶性胸膜间皮瘤的分子基础。

The Molecular Basis of Malignant Pleural Mesothelioma.

机构信息

Division of Thoracic Surgery, Brigham and Women's Hospital, Harvard Medical School, 75 Francis Street, Boston, MA 02115, USA.

Division of Thoracic Surgery, Brigham and Women's Hospital, Harvard Medical School, 75 Francis Street, Boston, MA 02115, USA.

出版信息

Thorac Surg Clin. 2020 Nov;30(4):383-393. doi: 10.1016/j.thorsurg.2020.08.005. Epub 2020 Sep 12.

DOI:10.1016/j.thorsurg.2020.08.005
PMID:33012428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7536355/
Abstract

Malignant pleural mesothelioma (MPM) is a rare, aggressive malignancy of the pleural lining associated with asbestos exposure in greater than 80% of cases. It is characterized by molecular heterogeneity both between patients and within individual tumors. Next-generation sequencing technology and novel computational techniques have resulted in a greater understanding of the epigenetic, genetic, and transcriptomic hallmarks of MPM. This article reviews these features and discusses the implications of advances in MPM molecular biology in clinical practice.

摘要

恶性胸膜间皮瘤(MPM)是一种罕见的、侵袭性的胸膜衬里恶性肿瘤,与 80%以上病例中的石棉暴露有关。它的特点是患者之间和单个肿瘤内的分子异质性。下一代测序技术和新型计算技术使人们对 MPM 的表观遗传、遗传和转录组特征有了更深入的了解。本文综述了这些特征,并讨论了 MPM 分子生物学进展在临床实践中的意义。

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本文引用的文献

1
Manipulating microRNAs for the Treatment of Malignant Pleural Mesothelioma: Past, Present and Future.调控微小RNA用于治疗恶性胸膜间皮瘤:过去、现在与未来
Front Oncol. 2020 Feb 7;10:105. doi: 10.3389/fonc.2020.00105. eCollection 2020.
2
Novel Germline Mutations in DNA Damage Repair in Patients with Malignant Pleural Mesotheliomas.恶性胸膜间皮瘤患者中 DNA 损伤修复相关种系新突变。
J Thorac Oncol. 2020 Apr;15(4):655-660. doi: 10.1016/j.jtho.2019.12.111. Epub 2019 Dec 28.
3
Epigenetic Regulation of miRNA Expression in Malignant Mesothelioma: miRNAs as Biomarkers of Early Diagnosis and Therapy.恶性间皮瘤中miRNA表达的表观遗传调控:miRNA作为早期诊断和治疗的生物标志物
Front Oncol. 2019 Nov 29;9:1293. doi: 10.3389/fonc.2019.01293. eCollection 2019.
4
Pleural mesothelioma and lung cancer: the role of asbestos exposure and genetic variants in selected iron metabolism and inflammation genes.胸膜间皮瘤和肺癌:石棉暴露和选定铁代谢和炎症基因遗传变异的作用。
J Toxicol Environ Health A. 2019;82(20):1088-1102. doi: 10.1080/15287394.2019.1694612. Epub 2019 Nov 22.
5
Autoimmunity, checkpoint inhibitor therapy and immune-related adverse events: A review.自身免疫、检查点抑制剂治疗和免疫相关不良事件:综述。
Semin Cancer Biol. 2020 Aug;64:93-101. doi: 10.1016/j.semcancer.2019.06.012. Epub 2019 Jul 19.
6
Mesothelioma: Scientific clues for prevention, diagnosis, and therapy.间皮瘤:预防、诊断和治疗的科学线索。
CA Cancer J Clin. 2019 Sep;69(5):402-429. doi: 10.3322/caac.21572. Epub 2019 Jul 8.
7
The Use of Radiation Therapy for the Treatment of Malignant Pleural Mesothelioma: Expert Opinion from the National Cancer Institute Thoracic Malignancy Steering Committee, International Association for the Study of Lung Cancer, and Mesothelioma Applied Research Foundation.《应用于恶性胸膜间皮瘤治疗的放射治疗:美国国家癌症研究所胸部恶性肿瘤指导委员会、国际肺癌研究协会以及间皮瘤应用研究基金会的专家意见》。
J Thorac Oncol. 2019 Jul;14(7):1172-1183. doi: 10.1016/j.jtho.2019.03.030. Epub 2019 May 22.
8
The role of apoptosis defects in malignant mesothelioma pathogenesis with an impact on prognosis and treatment.凋亡缺陷在恶性间皮瘤发病机制中的作用及其对预后和治疗的影响。
Cancer Chemother Pharmacol. 2019 Aug;84(2):241-253. doi: 10.1007/s00280-019-03878-3. Epub 2019 May 22.
9
Quantitative relationships of exposure to chrysotile asbestos and mesothelioma mortality.接触温石棉与间皮瘤死亡率的定量关系。
Am J Ind Med. 2019 Jun;62(6):471-477. doi: 10.1002/ajim.22985. Epub 2019 May 13.
10
Immune checkpoint inhibition for the treatment of mesothelioma.免疫检查点抑制治疗间皮瘤。
Expert Opin Biol Ther. 2019 Jul;19(7):697-706. doi: 10.1080/14712598.2019.1606209. Epub 2019 May 2.