Sasmita Andrew Octavian, Wong Ying Pei, Ling Anna Pick Kiong
Division of Applied Biomedical Sciences & Biotechnology, School of Health Sciences, International Medical University, Bukit Jalil, Kuala Lumpur, Malaysia.
Asia Pac J Clin Oncol. 2018 Feb;14(1):40-51. doi: 10.1111/ajco.12756. Epub 2017 Aug 25.
Glioblastoma multiforme (GBM) is a malignant tumor within the brain. Generally classified as primary and secondary with several different subtypes, ample molecular biomarkers have risen throughout the years which have garnered the attention of researchers. The advancements in genomics and proteomics have allowed researchers to gather prominent molecular biomarkers. All these biomarkers are gathered by means of biopsy or bodily fluid sample collection and are quantitatively analyzed by polymerase chain reaction coupled with other computational technologies. This review highlights the significance, regulation and prevalence of molecular biomarkers such as O -methylguanine-DNA methyltransferase, epidermal growth factor receptor vIII, isocitrate dehydrogenase mutation and several others which expressed differently in different types and molecular subtypes of GBM. The discoveries and roles of GBM-specific microRNAs including miR-21 and miR-10b as biomarkers with promising prognostic values were also delineated. The role and mechanism of biomarkers in GBM tumorigenesis are essential in the development of therapy for patients suffering from the disease itself. Thus, this review also discusses the mechanisms, effects and limitations of therapy such as temozolomide, viral gene transfer, biomarker-based vaccines or even engineered T cells for more specific responses. Biomarkers have displayed a high value and could eventually be utilized as drug targets. It is hoped that by combining different aspects of the disease which present with different biomarkers could lead to the development of a robust, effective and innovative take on GBM therapy.
多形性胶质母细胞瘤(GBM)是一种脑内恶性肿瘤。一般分为原发性和继发性,有几种不同的亚型,多年来出现了大量分子生物标志物,引起了研究人员的关注。基因组学和蛋白质组学的进展使研究人员能够收集到重要的分子生物标志物。所有这些生物标志物都是通过活检或收集体液样本获得的,并通过聚合酶链反应结合其他计算技术进行定量分析。本综述强调了分子生物标志物如O-甲基鸟嘌呤-DNA甲基转移酶、表皮生长因子受体vIII、异柠檬酸脱氢酶突变等在多形性胶质母细胞瘤不同类型和分子亚型中表达不同的意义、调控和普遍性。还阐述了包括miR-21和miR-10b在内的多形性胶质母细胞瘤特异性微小RNA作为具有潜在预后价值的生物标志物的发现和作用。生物标志物在多形性胶质母细胞瘤肿瘤发生中的作用和机制对于该疾病患者治疗的发展至关重要。因此,本综述还讨论了替莫唑胺、病毒基因转移、基于生物标志物的疫苗甚至工程化T细胞等治疗方法的机制、效果和局限性,以获得更特异性的反应。生物标志物已显示出很高的价值,最终可作为药物靶点。希望通过结合该疾病不同方面以及不同的生物标志物,能够开发出一种强大、有效且创新的多形性胶质母细胞瘤治疗方法。