Sun Huan H, Vaynblat Allen, Pass Harvey I
Department of Cardiothoracic Surgery, NYU School of Medicine, New York, NY, USA.
Stephen E. Banner Professor of Thoracic Oncology, Vice-Chair Research, Department of Cardiothoracic Surgery, NYU Langone Medical Center, New York, NY, USA.
Ann Transl Med. 2017 Jun;5(11):244. doi: 10.21037/atm.2017.06.60.
Malignant pleural mesothelioma (MPM) is an aggressive disease arising in pleural cell lining and is associated with asbestos exposure. Today, there is a rising incidence of MPM reaching 3,000 annual cases nationally, primarily from the large population occupationally exposed to asbestos between 1940 and 1980. With a prolonged latency period, presenting clinically 10 to 40 years after exposure, MPM is often diagnosed in late stages and presents median survival time of less than 12 months. There is a serious need for improvement in prognostic and diagnostic tools for MPM. Recent investigation and discovery of various biomarkers has shown promise, including Osteopontin, Fibulin-3, Soluble Mesothelin-Related Proteins (SMRP), High Mobility Group Box 1 (HMGB1), micro-RNA's, peripheral blood-based markers, and Slow Off-rate Modified Aptamer (SOMAmer) proteomic assays. In this review, we explore these current major biomarkers and their prognostic and diagnostic potential, highlighting the most recent large studies and developments for each. While progress has been made in mesothelioma research, many questions remain unanswered. Increased international cooperation is necessary for improving validity of results for current biomarkers through repeated investigation and increasing cohort sizes, as well as for the continued search for new and better markers.
恶性胸膜间皮瘤(MPM)是一种发生于胸膜细胞内衬的侵袭性疾病,与石棉暴露有关。如今,MPM的发病率呈上升趋势,全国每年有3000例病例,主要源于1940年至1980年间大量职业性接触石棉的人群。由于潜伏期较长,在接触后10至40年才出现临床症状,MPM往往在晚期才被诊断出来,中位生存时间不到12个月。迫切需要改进MPM的预后和诊断工具。最近对各种生物标志物的研究和发现显示出了前景,包括骨桥蛋白、纤连蛋白-3、可溶性间皮素相关蛋白(SMRP)、高迁移率族蛋白B1(HMGB1)、微小RNA、外周血标志物以及慢解离修饰适配体(SOMAmer)蛋白质组学检测。在这篇综述中,我们探讨了这些当前主要的生物标志物及其预后和诊断潜力,突出了每项标志物的最新大型研究和进展。虽然间皮瘤研究已取得进展,但许多问题仍未得到解答。通过反复研究和增加队列规模来提高当前生物标志物结果的有效性,以及持续寻找新的更好的标志物,都需要加强国际合作。