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恶性间皮瘤:从发病到治疗

Malignant mesothelioma: development to therapy.

作者信息

Thompson Joyce K, Westbom Catherine M, Shukla Arti

机构信息

Pathology Department, University of Vermont, College of Medicine, Burlington, Vermont.

出版信息

J Cell Biochem. 2014 Jan;115(1):1-7. doi: 10.1002/jcb.24642.

DOI:10.1002/jcb.24642
PMID:23959774
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3856563/
Abstract

Malignant mesothelioma (MM) is an aggressive cancer of the mesothelium caused by asbestos. Asbestos use has been reduced but not completely stopped. In addition, natural or man-made disasters will continue to dislodge asbestos from old buildings into the atmosphere and as long as respirable asbestos is available, MM will continue to be a threat. Due to the long latency period of MM development, it would still take decades to eradicate this disease if asbestos was completely removed from our lives today. Therefore, there is a need for researchers and clinicians to work together to understand this deadly disease and find a solution for early diagnosis and treatment. This article focuses on developmental mechanisms as well as current therapies available for MM.

摘要

恶性间皮瘤(MM)是一种由石棉引起的侵袭性间皮癌。石棉的使用已有所减少,但尚未完全停止。此外,自然或人为灾害将继续使石棉从旧建筑物中释放到大气中,只要有可吸入的石棉存在,MM就将继续构成威胁。由于MM发展的潜伏期很长,即使今天石棉已从我们的生活中完全消除,根除这种疾病仍需数十年时间。因此,研究人员和临床医生需要共同努力,了解这种致命疾病,并找到早期诊断和治疗的解决方案。本文重点关注MM的发病机制以及现有的治疗方法。

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本文引用的文献

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Phase II study of first-line bortezomib and cisplatin in malignant pleural mesothelioma and prospective validation of progression free survival rate as a primary end-point for mesothelioma clinical trials (European Organisation for Research and Treatment of Cancer 08052).硼替佐米联合顺铂一线治疗恶性胸膜间皮瘤的 II 期研究及前瞻性验证无进展生存率作为间皮瘤临床试验的主要终点(欧洲癌症研究与治疗组织 08052)。
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Radical pleurectomy and chemoradiation for malignant pleural mesothelioma: the outcome of incomplete resections.根治性胸膜切除术和放化疗治疗恶性胸膜间皮瘤:不完全切除的结果。
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Accurate diagnosis of mesothelioma: more important than ever.间皮瘤的准确诊断:比以往任何时候都更重要。
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Synergistic anticancer activity of arsenic trioxide with erlotinib is based on inhibition of EGFR-mediated DNA double-strand break repair.三氧化二砷与厄洛替尼协同抗癌作用的机制是抑制 EGFR 介导的 DNA 双链断裂修复。
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Extracellular signal-regulated kinase 5: a potential therapeutic target for malignant mesotheliomas.细胞外信号调节激酶 5:恶性间皮瘤的潜在治疗靶点。
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Changes of mesothelin and osteopontin levels over time in formerly asbestos-exposed power industry workers.曾暴露于石棉的电力行业工人中,间皮素和骨桥蛋白水平随时间的变化。
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