Steponaitis Giedrius, Kazlauskas Arunas, Skiriute Daina, Vaitkiene Paulina, Skauminas Kestutis, Tamasauskas Arimantas
Laboratory of Molecular Neurooncology, Neuroscience Institute, Lithuanian University of Health Sciences, Eiveniu str. 4, Kaunas, LT 50161, Lithuania.
J Cancer. 2019 Feb 23;10(6):1479-1488. doi: 10.7150/jca.29282. eCollection 2019.
Amphiregulin (AREG) is one of the ligands of the epidermal growth factor receptor which levels was shown to have a tight coherence with various types of cancer. AREG was also designated to be a promising marker for several types of cancer however precious little data about AREG role in the most frequent and generally lethal human brain tumours - astrocytomas reported up to date. The aim of the study was to investigate how AREG changes at epigenetic and expression levels reflect on astrocytoma malignancy and patient outcome. : In total 205 low and high grade astrocytoma samples (15 pilocytic astrocytomas, 56 diffuse astrocytomas, 32 anaplastic astrocytomas and 102 glioblastomas) were used for target mRNA, protein expression and DNA methylation analysis applying qRT-PCR, Western-Blot and MS-PCR assays, respectively. Present research revealed that AREG expression level and methylation in cancer tissue is dependent on the grade of astrocytoma. GBM tissue disclosed elevated AREG mRNA expression but reduced AREG protein level as compared to grade II and grade III astrocytomas (p<0.001). Increased methylation frequency was also more abundant in GBM (74%) than grade I, II and III astrocytomas (25%, 34%, and 36%, respectively). The survival analysis revealed relevant differences in patient overall survival between AREG methylation, mRNA and protein expression groups. Kaplan-Meier analysis encompassing only malignant tumours showed similar results indicating that AREG is associated with astrocytoma patient survival independently from astrocytoma grade. Current findings demonstrate that AREG appearance is associated with patient survival as well as astrocytomas malignancy indicating its influence on tumour progression and suggest its applicability as a promising marker.
双调蛋白(AREG)是表皮生长因子受体的配体之一,其水平与多种类型的癌症密切相关。AREG也被认为是几种癌症的有前景的标志物,然而,迄今为止,关于AREG在最常见且通常致命的人类脑肿瘤——星形细胞瘤中的作用的数据却非常少。本研究的目的是探讨AREG在表观遗传和表达水平上的变化如何反映星形细胞瘤的恶性程度和患者预后。总共205个低级别和高级别星形细胞瘤样本(15个毛细胞型星形细胞瘤、56个弥漫性星形细胞瘤、32个间变性星形细胞瘤和102个胶质母细胞瘤)分别用于通过qRT-PCR、蛋白质免疫印迹和甲基化特异性PCR分析来检测靶mRNA、蛋白质表达和DNA甲基化。目前的研究表明,癌组织中AREG的表达水平和甲基化情况取决于星形细胞瘤的分级。与II级和III级星形细胞瘤相比,胶质母细胞瘤组织中AREG mRNA表达升高,但AREG蛋白水平降低(p<0.001)。胶质母细胞瘤中甲基化频率增加(74%)也比I级、II级和III级星形细胞瘤(分别为25%、34%和36%)更为常见。生存分析显示,AREG甲基化、mRNA和蛋白质表达组之间患者的总生存期存在显著差异。仅对恶性肿瘤进行的Kaplan-Meier分析显示了类似的结果,表明AREG与星形细胞瘤患者的生存相关,独立于星形细胞瘤分级。目前的研究结果表明,AREG的表现与患者生存以及星形细胞瘤的恶性程度相关,表明其对肿瘤进展有影响,并提示其作为一种有前景的标志物的适用性。