Zhang Xinbo, Tang Naimei, Rishi Arun K, Pass Harvey I, Wali Anil
Department of Oncology, Karmanos Cancer Institute, Wayne State University and John D. Dingell VA Medical Center, Detroit, MI, 48201, USA.
Methods Mol Biol. 2015;1238:235-47. doi: 10.1007/978-1-4939-1804-1_12.
Malignant Pleural Mesothelioma (MPM) is an aggressive malignancy of the pleura associated with asbestos exposure. Incidence of MPM is expected to increase over the course of next decade in both Europe and the developing countries. Although significant progress has been made in terms of etiology and pathogenesis of this disease, currently available therapeutic options have not significantly improved the survival outcome of patients on standard chemotherapeutic regimens. Integrity of the cellular DNA is often altered in many cancers. Understanding of the molecular mechanisms that regulate cellular DNA alterations to facilitate cancer initiation and development has potential to allow better design of cancer cell inhibitory strategies. In this context, there is a need to explore the gamut of "omics" strategies to provide a comprehensive epigenetics profile for MPM. This chapter discusses the functional genomics and epigenetic patterns observed by various investigators studying MPM patient populations on global fronts, and attempts to present a holistic approach in combating this insidious disease. Here we provide investigators in this field with novel insights and methodologies used in other types of cancers that might have profound impact in the early detection, prognosis and potential therapeutic strategies for MPM.
恶性胸膜间皮瘤(MPM)是一种与接触石棉相关的侵袭性胸膜恶性肿瘤。预计在未来十年,欧洲和发展中国家的MPM发病率都将上升。尽管在该疾病的病因和发病机制方面已取得显著进展,但目前可用的治疗方案并未显著改善接受标准化疗方案患者的生存结局。在许多癌症中,细胞DNA的完整性常常发生改变。了解调节细胞DNA改变以促进癌症发生和发展的分子机制,有可能使癌细胞抑制策略的设计更加完善。在这种背景下,有必要探索一系列“组学”策略,以提供MPM全面的表观遗传学特征。本章讨论了不同研究人员在全球范围内对MPM患者群体进行研究时观察到的功能基因组学和表观遗传模式,并试图提出一种整体方法来对抗这种隐匿性疾病。在此,我们为该领域的研究人员提供在其他类型癌症中使用的新颖见解和方法,这些见解和方法可能对MPM的早期检测、预后及潜在治疗策略产生深远影响。