Laboratory of Genetics and Molecular Pathology, Institute of Pathology, Ente Ospedaliero Cantonale (EOC), 6900 Locarno, Switzerland.
Service of Neurosurgery, Neurocenter of the Southern Switzerland, Regional Hospital of Lugano, Ente Ospedaliero Cantonale (EOC), 6900 Lugano, Switzerland.
Cells. 2024 Feb 2;13(3):276. doi: 10.3390/cells13030276.
Glioblastoma multiforme (GBM) is usually treated with surgery followed by adjuvant partial radiotherapy combined with temozolomide (TMZ) chemotherapy. Recent studies demonstrated a better survival and good response to TMZ in methylguanine-DNA methyltransferase ()-methylated GBM cases. However, approximately 20% of patients with -unmethylated GBM display an unexpectedly favorable outcome. Therefore, additional mechanisms related to the TMZ response need to be investigated. As such, we decided to investigate the clinical relevance of six miRNAs involved in brain tumorigenesis (miR-181c, miR-181d, miR-21, miR-195, miR-196b, miR-648) as additional markers of response and survival in patients receiving TMZ for GBM. We evaluated miRNA expression and the interplay between miRNAs in 112 wt GBMs by applying commercial assays. Then, we correlated the miRNA expression with patients' clinical outcomes. Upon bivariate analyses, we found a significant association between the expression levels of the miRNAs analyzed, but, more interestingly, the OS curves show that the combination of low miR-648 and miR-181c or miR-181d expressions is associated with a worse prognosis than cases with other low-expression miRNA pairs. To conclude, we found how specific miRNA pairs can influence survival in GBM cases treated with TMZ.
多形性胶质母细胞瘤(GBM)通常采用手术治疗,然后辅以辅助局部放疗联合替莫唑胺(TMZ)化疗。最近的研究表明,在甲基鸟嘌呤-DNA 甲基转移酶(MGMT)-甲基化的 GBM 病例中,TMZ 治疗的生存率更高,反应更好。然而,约 20%的未甲基化 GBM 患者表现出出乎意料的良好预后。因此,需要研究与 TMZ 反应相关的其他机制。因此,我们决定研究与脑肿瘤发生相关的六种 miRNA(miR-181c、miR-181d、miR-21、miR-195、miR-196b、miR-648)作为接受 TMZ 治疗的 GBM 患者反应和生存的附加标志物的临床相关性。我们通过应用商业检测评估了 112 例 wt GBM 中的 miRNA 表达及其相互作用。然后,我们将 miRNA 表达与患者的临床结果相关联。在双变量分析中,我们发现分析的 miRNA 表达水平之间存在显著关联,但更有趣的是,OS 曲线表明,miR-648 和 miR-181c 或 miR-181d 表达水平低的组合与预后较差相关,而其他低表达 miRNA 组合的病例预后较好。总之,我们发现特定的 miRNA 对可以如何影响接受 TMZ 治疗的 GBM 病例的生存。