Department of Neurosurgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Avenue, Wuhan, 430022, China.
J Transl Med. 2022 Jul 25;20(1):335. doi: 10.1186/s12967-022-03536-y.
Glioma is the most common cancer in the central nervous system, and low grade gliomas are notorious for many types of tumors and heterogeneity. PROS1 not only plays an important role in the blood coagulation system, and recent studies have found that it was correlated with the development of tumors, especially related to tumor immune infiltration. However, the study of underlying role and mechanism of PROS1 in gliomas, especially in low-grade gliomas, is almost absent.
We integrated the information of patients with LGG in The Cancer Genome Atlas (TCGA) cohort and Chinese Glioma Genome Atlas (CGGA) cohort. Then, we systematically demonstrated the differences and prognostic prognosis value of PROS1 based on multi-omics analyses. In addition, Cell counting kit-8 (CCK-8) assay, colony formation assay, 5-Ethynyl-2'-deoxyuridine (EdU) incorporation assay, and Transwell assays were performed to evaluate cell proliferation and invasion. qRT-PCR and immunohistochemistry were used to evaluate the expression of PROS1 in LGG.
Various bioinformatics approaches revealed that PROS1 was a valuable prognostic marker and may influence tumour development via distinct mechanisms, including expression of DNA methyltransferase, RNA modification, and DNA mismatch repair system genes, copy number variation, single nucleotide variation frequency, genomic heterogeneity, cancer stemness, DNA methylation, and alternative PROS1 splicing. Our analyses indicated that the long non-coding RNA RP3-525N10.2 may "decoy" or "guide" the transcription factor NFKB1 and prevent its association with PROS1, thereby reducing PROS1 expression and improving poor LGG prognosis. PROS1 expression was also closely associated with tumour infiltration by immune cells, especially tumour-associated macrophages, as well as the expression of various immune checkpoint inhibitors, immunomodulators, and immune cell markers.
long non-coding RNA RP3-525N10.2-NFKB1-PROS1 triplet-mediated PROS1 expression could serve as a biomarker for cancer diagnosis, prognosis, therapy selection, and follow-up in LGG patients.
神经胶质瘤是中枢神经系统最常见的癌症,而低级神经胶质瘤因其多种类型的肿瘤和异质性而臭名昭著。PROS1 不仅在凝血系统中发挥重要作用,而且最近的研究发现它与肿瘤的发生有关,特别是与肿瘤免疫浸润有关。然而,PROS1 在神经胶质瘤中的潜在作用和机制研究,特别是在低级别神经胶质瘤中,几乎是空白的。
我们整合了 TCGA 队列和 CGGA 队列中 LGG 患者的信息。然后,我们系统地展示了基于多组学分析的 PROS1 的差异和预后预测价值。此外,我们通过细胞计数试剂盒-8 (CCK-8) 测定、集落形成测定、5-乙炔基-2'-脱氧尿苷 (EdU) 掺入测定和 Transwell 测定来评估细胞增殖和侵袭。qRT-PCR 和免疫组织化学用于评估 LGG 中 PROS1 的表达。
各种生物信息学方法表明,PROS1 是一个有价值的预后标志物,可能通过不同的机制影响肿瘤的发展,包括 DNA 甲基转移酶、RNA 修饰和 DNA 错配修复系统基因、拷贝数变异、单核苷酸变异频率、基因组异质性、癌症干性、DNA 甲基化和替代 PROS1 剪接的表达。我们的分析表明,长非编码 RNA RP3-525N10.2 可能“诱饵”或“引导”转录因子 NFKB1 并阻止其与 PROS1 结合,从而降低 PROS1 的表达并改善 LGG 的不良预后。PROS1 的表达也与肿瘤浸润免疫细胞密切相关,特别是肿瘤相关巨噬细胞,以及各种免疫检查点抑制剂、免疫调节剂和免疫细胞标志物的表达。
长非编码 RNA RP3-525N10.2-NFKB1-PROS1 三重介导的 PROS1 表达可作为 LGG 患者癌症诊断、预后、治疗选择和随访的生物标志物。