Chen Zhongjian, Gaudino Giovanni, Pass Harvey I, Carbone Michele, Yang Haining
University of Hawaii Cancer Center, Honolulu, HI, USA.
Department of pharmacy, Zhejiang Cancer Hospital, Hangzhou 310022, China.
Transl Lung Cancer Res. 2017 Jun;6(3):259-269. doi: 10.21037/tlcr.2017.05.06.
Malignant mesothelioma (MM) is an aggressive and lethal cancer, mostly related to inhalation of asbestos and erionite fibers. MM is associated with poor prognosis, because of its resistance to current therapies, even if higher survival occurs in patients diagnosed and treated when at stage I of the disease. However, these do not exceed 5% of the total number of cases, due to the inadequacy of the existing biomarkers for early and accurate diagnosis. Therefore, new effective biomarkers are needed for MM detection at earlier stages and to develop tailored therapies. Here we review the most promising biomarkers in MM to date: mesothelin, soluble mesothelin-related peptides (SMRPs), megakaryocyte potentiating factor (MPF), Osteopontin (OPN), Fibulin-3, high mobility group B1 (HMGB1), microRNAs (miRNAs), multiplex protein signatures. The validation of these biomarkers will allow their use, alone or in combination, for monitoring individuals from cohorts at risk of MM and attaining early detection of MM that is instrumental in improving patient survival.
恶性间皮瘤(MM)是一种侵袭性和致命性癌症,主要与吸入石棉和毛沸石纤维有关。MM预后较差,因为它对当前疗法具有抗性,即使疾病处于I期时被诊断和治疗的患者生存率较高。然而,由于现有生物标志物在早期准确诊断方面存在不足,这些患者在病例总数中所占比例不超过5%。因此,需要新的有效生物标志物用于MM的早期检测并开发个性化疗法。在此,我们综述了迄今为止MM中最有前景的生物标志物:间皮素、可溶性间皮素相关肽(SMRP)、巨核细胞增强因子(MPF)、骨桥蛋白(OPN)、纤连蛋白-3、高迁移率族蛋白B1(HMGB1)、微小RNA(miRNA)、多重蛋白质特征。这些生物标志物的验证将允许单独或联合使用它们来监测MM风险队列中的个体,并实现MM的早期检测,这有助于提高患者生存率。