PK-Neurooncology Research Group, Institute of Basic Medical Sciences, Khyber Medical University, Peshawar 25100, Pakistan; Department of Biological Sciences, Faculty of Science, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Department of Anatomy, Institute of Basic Medical Sciences, Khyber Medical University, Peshawar 25100, Pakistan.
Semin Cancer Biol. 2018 Oct;52(Pt 1):85-102. doi: 10.1016/j.semcancer.2017.07.004. Epub 2017 Jul 31.
Recent investments in research associated with the discovery of specific tumor biomarkers important for efficient diagnosis and prognosis are beginning to bear fruit. Key biomarkers could potentially outweigh traditional radiological or pathological methods by enabling specificity of early detection, when coupled with tumor molecular profiling and clinical associations. Only few biomarkers are approved by regulatory authorities for Central Nervous System Tumors (CNSTs), despite the evaluation of a large number of CNST related markers during clinical trials. Traditional CNSTs biomarkers include 1p/19q co-deletion, O6-Methylguanine-DNA Methyltransferase Methylation, and mutations in IDH1/IDH2. Recently tested CNSTs biomarkers include VEGFR-2, EGFRvIII, IL2, PDGFR, MMPs, BRAF, STAT3, PTEN, TERT, AKT, NF2, and BCL2. Additional studies have highlighted new and novel MicroRNAs, circular RNAs and long non-coding RNAs as promising biomarkers. Studies on microvesicles pinpoint exosomes as promising, less invasive biomarkers that could be isolated from the serum of cancer patients. Furthermore, Cancer Stem Cells (CSCs) related molecules, such as CD133, SOX2 and Nestin, utilized as CNST biomarkers, might enable efficient monitoring of cancer progression, and/or surveillance of emerging drug resistant cells. Approved protocols that implement novel molecular markers in diagnostics, prognostics and drug development will herald a new era of precision and personalized neuro-oncology. This review summarizes and discusses putative CNST biomarkers that are under clinical development, and are ready to move into diagnostic, prognostic and therapeutic applications. Data presented here is predicted to aid in streamlining the process of biomarker's research and development.
最近在与发现对高效诊断和预后至关重要的特定肿瘤生物标志物相关的研究方面的投资开始取得成果。关键生物标志物有可能通过与肿瘤分子谱分析和临床关联相结合,实现早期检测的特异性,从而超越传统的放射学或病理学方法。尽管在临床试验中评估了大量与 CNS 肿瘤(CNST)相关的标志物,但只有少数生物标志物获得监管机构批准用于 CNST。传统的 CNS 肿瘤标志物包括 1p/19q 共缺失、O6-甲基鸟嘌呤-DNA 甲基转移酶甲基化和 IDH1/IDH2 突变。最近测试的 CNS 肿瘤标志物包括 VEGFR-2、EGFRvIII、IL2、PDGFR、MMPs、BRAF、STAT3、PTEN、TERT、AKT、NF2 和 BCL2。其他研究还强调了新的和新型 MicroRNAs、环状 RNA 和长非编码 RNA 作为有前途的生物标志物。关于微泡的研究指出,外泌体作为有前途的、微创的生物标志物,可以从癌症患者的血清中分离出来。此外,作为 CNS 肿瘤标志物使用的癌症干细胞(CSC)相关分子,如 CD133、SOX2 和 Nestin,可能能够有效地监测癌症进展和/或监测新出现的耐药细胞。将新的分子标志物应用于诊断、预后和药物开发的批准方案将开创精准神经肿瘤学和个性化神经肿瘤学的新时代。这篇综述总结和讨论了正在临床开发的潜在 CNS 肿瘤标志物,并准备将其应用于诊断、预后和治疗。这里提出的数据有望帮助简化生物标志物的研究和开发过程。