参与高压氧治疗胶质母细胞瘤有益机制的关键基因以及高压氧延长胶质母细胞瘤患者生存期的预测指标。

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Current Medical Science Pub Date : 2024-10-01 Epub Date: 2024-10-24 DOI:10.1007/s11596-024-2934-7
Zi-Qi Ren, Ren-Dong Wang, Cong Wang, Xiao-Hui Ren, Dong-Guo Li, Ya-Ling Liu, Qiu-Hong Yu
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引用次数: 0

摘要

目的:胶质母细胞瘤的预后很差,耐药性主要归因于肿瘤内缺氧。高压氧(HBO)能有效缓解缺氧。然而,高压氧在胶质母细胞瘤中的唯一作用仍存在争议。我们以前曾报道过高压氧能促进胶质母细胞瘤细胞凋亡、缩短突起和延缓生长,但其分子机制尚不清楚。我们的目的是检测暴露于HBO的胶质母细胞瘤细胞中的候选基因,并分析它们与胶质母细胞瘤患者生存期的相关性:方法:收集暴露于重复HBO或常压空气(NBA)的胶质母细胞瘤细胞系,进行RNA分离和芯片数据分析。对差异表达基因(DEGs)进行了GO分析、KEGG通路分析和生存分析:结果:HBO不仅抑制了CA9、FGF11、PPFIA4、TCAF2和SLC2A12等缺氧诱导基因,还通过下调COL1A1、COL8A1、COL12A1、RHOJ和FILIP1L的表达调控血管生成,最终减轻了胶质母细胞瘤的缺氧微环境。HBO 通过减少 NLRP2、CARD8、MYD88 和 CD180 的表达来减轻炎性微环境。HBO 通过下调 NTM、CXCL12、CXCL13、CXCR4、CXCR5、CDC42、IGFBP3、IGFBP5、GPC6、MMP19、ADAMTS1、EFEMP1、PTBP3、NF1 和 PDCD1 的表达防止转移。HBO 上调了 BAK1、PPIF、DDIT3、TP53I11 和 FAS 的表达,同时下调了 MDM4 和 SIVA1 的表达,从而促进了细胞凋亡。HBO 上调 CDC25A、MCM2、PCNA、RFC33、DSCC1 和 CDC14A 的表达,而下调 ASNS、CDK6、CDKN1B、PTBP3 和 MAD2L1 的表达,从而抑制细胞周期的进展。在这些DEGs中,检测到了17个HBO延长生存期的指标基因:结论:HBO 对胶质母细胞瘤有益。结论:HBO 对胶质母细胞瘤有益,具有这些预测指标的胶质母细胞瘤患者可通过 HBO 治疗延长生存期。这些潜在的治疗靶点,尤其是COL1A1、ADAMTS1和PTBP3,值得进一步验证。
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Key Genes Involved in the Beneficial Mechanism of Hyperbaric Oxygen for Glioblastoma and Predictive Indicators of Hyperbaric Oxygen Prolonging Survival in Glioblastoma Patients.

Objective: The prognosis of glioblastoma is poor, and therapy-resistance is largely attributed to intratumor hypoxia. Hyperbaric oxygen (HBO) effectively alleviates hypoxia. However, the sole role of HBO in glioblastoma remains controversial. We previously reported that HBO can promote apoptosis, shorten protrusions, and delay growth of glioblastoma, but the molecular mechanism is unclear. We aimed to test candidate genes in HBO-exposed glioblastoma cells and to analyze their correlation with the survival of glioblastoma patients.

Methods: Glioblastoma cell lines exposed to repetitive HBO or normobaric air (NBA) were collected for RNA isolation and microarray data analysis. GO analysis, KEGG pathway analysis and survival analysis of the differentially expressed genes (DEGs) were performed.

Results: HBO not only inhibited hypoxia-inducing genes including CA9, FGF11, PPFIA4, TCAF2 and SLC2A12, but also regulated vascularization by downregulating the expression of COL1A1, COL8A1, COL12A1, RHOJ and FILIP1L, ultimately attenuated hypoxic microenvironment of glioblastoma. HBO attenuated inflammatory microenvironment by reducing the expression of NLRP2, CARD8, MYD88 and CD180. HBO prevented metastasis by downregulating the expression of NTM, CXCL12, CXCL13, CXCR4, CXCR5, CDC42, IGFBP3, IGFBP5, GPC6, MMP19, ADAMTS1, EFEMP1, PTBP3, NF1 and PDCD1. HBO upregulated the expression of BAK1, PPIF, DDIT3, TP53I11 and FAS, whereas downregulated the expression of MDM4 and SIVA1, thus promoting apoptosis. HBO upregulated the expression of CDC25A, MCM2, PCNA, RFC33, DSCC1 and CDC14A, whereas downregulated the expression of ASNS, CDK6, CDKN1B, PTBP3 and MAD2L1, thus inhibiting cell cycle progression. Among these DEGs, 17 indicator-genes of HBO prolonging survival were detected.

Conclusions: HBO is beneficial for glioblastoma. Glioblastoma patients with these predictive indicators may prolong survival with HBO therapy. These potential therapeutic targets especially COL1A1, ADAMTS1 and PTBP3 deserve further validation.

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来源期刊
Current Medical Science
Current Medical Science Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
4.70
自引率
0.00%
发文量
126
期刊介绍: Current Medical Science provides a forum for peer-reviewed papers in the medical sciences, to promote academic exchange between Chinese researchers and doctors and their foreign counterparts. The journal covers the subjects of biomedicine such as physiology, biochemistry, molecular biology, pharmacology, pathology and pathophysiology, etc., and clinical research, such as surgery, internal medicine, obstetrics and gynecology, pediatrics and otorhinolaryngology etc. The articles appearing in Current Medical Science are mainly in English, with a very small number of its papers in German, to pay tribute to its German founder. This journal is the only medical periodical in Western languages sponsored by an educational institution located in the central part of China.
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