胸膜间皮瘤基因谱的诊断、预后和治疗意义

IF 1.4 Q4 ONCOLOGY
A. Sadek, A. De Rienzo, R. Bueno
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引用次数: 0

摘要

胸膜间皮瘤(PM)是一种侵袭性恶性胸膜衬里,通常继发于石棉暴露。随着新一代测序技术的出现,过去三十年来胸膜间皮瘤的分子特征研究取得了重大进展。然而,这些进展在很大程度上无法确定PM的有效靶向治疗方法。此外,在分期和治疗方面仍然缺乏公认的金标准共识,这在一定程度上解释了PM患者总体预后不良的原因。近年来,PM肿瘤的基因谱分析已被证明是PM诊断和预后的有效工具。基因组测序已经确定了几个潜在的目标,开发新的治疗方法在PM。本文综述了PM肿瘤的基因组学和肿瘤谱在诊断、预后和治疗方面的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic, prognostic, and therapeutic implications of genetic profiling in pleural mesothelioma
Pleural mesothelioma (PM) is an aggressive malignancy of the pleural lining that typically arises secondary to asbestos exposure. With the advent of next-generation sequencing, major progress has been made in the molecular characterization of pleural mesothelioma over the past three decades. However, these advances have been largely unable to identify effective targeted therapies for PM. Additionally, there remains an absence of accepted gold-standard consensus for staging and treatment, which partly explains the overall poor outcomes in patients with PM. In recent years, genetic profiling of PM tumors has proved to be an effective tool in the diagnosis and prognosis of PM. Genomic sequencing has identified several potential targets for the development of novel therapeutics in PM. This review summarizes the progress in diagnosis, prognosis, and therapeutics derived by genomics and tumor profiling of PM tumors.
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来源期刊
CiteScore
3.20
自引率
5.30%
发文量
460
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