Department of Pathology, Children's Cancer Hospital Egypt 57357, Cairo, Egypt.
Department of Molecular Diagnostics, Genetic Engineering and Biotechnology Research Institute, University of Sadat City, Menoufia, Egypt.
Sci Rep. 2019 Aug 30;9(1):12605. doi: 10.1038/s41598-019-49027-x.
Aggresomes are inclusion bodies for misfolded/aggregated proteins. Despite the role of misfolded/aggregated proteins in neurological disorders, their role in cancer pathogenesis is poorly defined. In the current study we aimed to investigate whether aggresomes-positivity could be used to improve the disease subclassification and prognosis prediction of pediatric medulloblastoma. Ninety three pediatric medulloblastoma tumor samples were retrospectively stratified into three molecular subgroups; WNT, SHH and non-WNT/non-SHH, using immunohistochemistry and Multiplex Ligation Probe Amplification. Formation of aggresomes were detected using immunohistochemistry. Overall survival (OS) and event-free survival (EFS) were determined according to risk stratification criteria. Multivariate Cox regression analyses were carried out to exclude confounders. Aggresomes formation was detected in 63.4% (n = 59/93) of samples. Aggresomes were non-randomly distributed among different molecular subgroups (P = 0.00002). Multivariate Cox model identified aggresomes' percentage at ≥20% to be significantly correlated with patient outcome in both OS (HR = 3.419; 95% CI, 1.30-8.93; P = 0.01) and EFS (HR = 3; 95% CI, 1.19-7.53; P = 0.02). The presence of aggresomes in ≥20% of the tumor identified poor responders in standard risk patients; OS (P = 0.02) and EFS (P = 0.06), and significantly correlated with poor outcome in non-WNT/non-SHH molecular subgroup; OS (P = 0.0002) and EFS (P = 0.0004).
聚集物是错误折叠/聚集蛋白的包涵体。尽管错误折叠/聚集蛋白在神经疾病中起作用,但它们在癌症发病机制中的作用尚未明确。在本研究中,我们旨在研究聚集物阳性是否可用于改善小儿髓母细胞瘤的疾病亚分类和预后预测。使用免疫组织化学和多重连接探针扩增法,回顾性地将 93 例小儿髓母细胞瘤肿瘤样本分为 WNT、SHH 和非 WNT/非 SHH 三个分子亚组。使用免疫组织化学检测聚集物的形成。根据危险分层标准确定总生存期(OS)和无事件生存期(EFS)。进行多变量 Cox 回归分析以排除混杂因素。在 63.4%(n=59/93)的样本中检测到聚集物形成。聚集物在不同分子亚组中的分布是非随机的(P=0.00002)。多变量 Cox 模型确定≥20%的聚集物百分比与 OS(HR=3.419;95%CI,1.30-8.93;P=0.01)和 EFS(HR=3;95%CI,1.19-7.53;P=0.02)的患者结局显著相关。≥20%的肿瘤中存在聚集物可识别标准风险患者的低反应者;OS(P=0.02)和 EFS(P=0.06),并且与非 WNT/非 SHH 分子亚组的不良结局显著相关;OS(P=0.0002)和 EFS(P=0.0004)。