Lu Weicheng, Chen Hong, Liang Bo, Ou Chaopeng, Zhang Mingwei, Yue Qiuyuan, Xie Jingdun
State Key Laboratory of Oncology in Southern China, Department of Anesthesiology, Sun Yat-sen University Cancer Center, Collaborative Innovation for Cancer Medicine, Guangzhou, China.
Department of Gastrointestinal Surgery, Fujian Provincial Hospital, Fuzhou, China.
Front Mol Biosci. 2021 Oct 13;8:736947. doi: 10.3389/fmolb.2021.736947. eCollection 2021.
Glioblastoma multiform is a lethal primary brain tumor derived from astrocytic, with a poor prognosis in adults. Reticulocalbin-1 (RCN1) is a calcium-binding protein, dysregulation of which contributes to tumorigenesis and progression in various cancers. The present study aimed to identify the impact of RCN1 on the outcomes of patients with Glioblastoma multiforme (GBM). The study applied two public databases to require RNA sequencing data of Glioblastoma multiform samples with clinical data for the construction of a training set and a validation set, respectively. We used bioinformatic analyses to determine that RCN1 could be an independent factor for the overall survival of Glioblastoma multiform patients. In the training set, the study constructed a predictive prognostic model based on the combination of RCN1 with various clinical parameters for overall survival at 0.5-, 1.0-, and 1.5-years, as well as developed a nomogram, which was further validated by validation set. Pathways analyses indicated that RCN1 was involved in KEAS and MYC pathways and apoptosis. experiments indicated that RCN1 promoted cell invasion of Glioblastoma multiform cells. These results illustrated the prognostic role of RCN1 for overall survival in Glioblastoma multiform patients, indicated the promotion of RCN1 in cell invasion, and suggested the probability of RCN1 as a potential targeted molecule for treatment in Glioblastoma multiform.
多形性胶质母细胞瘤是一种源自星形细胞的致命性原发性脑肿瘤,成人患者预后较差。网钙蛋白-1(RCN1)是一种钙结合蛋白,其失调在多种癌症的肿瘤发生和进展中起作用。本研究旨在确定RCN1对多形性胶质母细胞瘤(GBM)患者预后的影响。该研究应用两个公共数据库,分别获取多形性胶质母细胞瘤样本的RNA测序数据及临床数据,以构建训练集和验证集。我们通过生物信息学分析确定RCN1可能是多形性胶质母细胞瘤患者总生存的独立因素。在训练集中,该研究基于RCN1与各种临床参数的组合构建了预测0.5年、1年和1.5年总生存的预后模型,并绘制了列线图,该列线图在验证集中得到进一步验证。通路分析表明RCN1参与KEAS和MYC通路以及细胞凋亡。实验表明RCN1促进多形性胶质母细胞瘤细胞的侵袭。这些结果阐明了RCN1在多形性胶质母细胞瘤患者总生存中的预后作用,表明RCN1促进细胞侵袭,并提示RCN1作为多形性胶质母细胞瘤潜在治疗靶点分子的可能性。