• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

研究脑胶质母细胞瘤的基因和 microRNA 表达。

Investigation gene and microRNA expression in glioblastoma.

机构信息

State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences and Institutes of Biomedical Sciences, Fudan University, Shanghai 200433, China.

出版信息

BMC Genomics. 2010 Dec 1;11 Suppl 3(Suppl 3):S16. doi: 10.1186/1471-2164-11-S3-S16.

DOI:10.1186/1471-2164-11-S3-S16
PMID:21143783
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2999346/
Abstract

BACKGROUND

Glioblastoma is the most common primary brain tumor in adults. Though a lot of research has been focused on this disease, the causes and pathogenesis of glioblastoma have not been indentified clearly.

RESULTS

We indentified 1,236 significantly differentially expressed genes, and 30 pathways enriched in the set of differentially expressed genes among 243 tumor and 11 normal samples. We also indentified 97 differentially expressed microRNAs among 240 tumor and 10 normal samples. 22 of which have been reported to affect glioblastoma and 50 of which were implicated in other cancers and brain diseases. We regressed gene expression on microRNA expression in 237 tumor tissues and 10 normal tissues comprehensively. We found two experimentally validated microRNA targets and 1,094 miRNA-target gene pairs in our datasets which were predicted by miRanda algorithm, 8 of the target genes were tumor suppressor genes and 3 were oncogenes. Further function analysis of target genes suggested that microRNAs most frequently targeted genes associated with Cell Signalling and Nervous System.

CONCLUSION

We investigated gene and microRNA Expression in Glioblastoma and gave a comprehensive function study of differential expressed gene and microRNA in glioblastoma patients. These findings gave important clues to study of the carcinogenic process in glioblastomas.

摘要

背景

胶质母细胞瘤是成人中最常见的原发性脑肿瘤。尽管针对这种疾病已经开展了大量研究,但胶质母细胞瘤的病因和发病机制仍未明确。

结果

我们在 243 个肿瘤样本和 11 个正常样本的差异表达基因集中鉴定出 1236 个显著差异表达基因和 30 条富集途径。我们还在 240 个肿瘤样本和 10 个正常样本中鉴定出 97 个差异表达 microRNA。其中 22 个已经被报道会影响胶质母细胞瘤,50 个则与其他癌症和脑部疾病有关。我们综合分析了 237 个肿瘤组织和 10 个正常组织中的基因表达和 microRNA 表达,在我们的数据集里发现了两个经过实验验证的 microRNA 靶标和 1094 个由 miRanda 算法预测的 miRNA-靶基因对,其中 8 个靶基因是肿瘤抑制基因,3 个是癌基因。对靶基因的进一步功能分析表明,microRNAs 最常靶向与细胞信号转导和神经系统相关的基因。

结论

我们研究了胶质母细胞瘤中的基因和 microRNA 表达,并对胶质母细胞瘤患者的差异表达基因和 microRNA 进行了全面的功能研究。这些发现为研究胶质母细胞瘤中的致癌过程提供了重要线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/2999346/08cac0d430fe/1471-2164-11-S3-S16-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/2999346/93ff3f16a4f4/1471-2164-11-S3-S16-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/2999346/5b667820d9fa/1471-2164-11-S3-S16-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/2999346/588da63e21d5/1471-2164-11-S3-S16-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/2999346/08cac0d430fe/1471-2164-11-S3-S16-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/2999346/93ff3f16a4f4/1471-2164-11-S3-S16-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/2999346/5b667820d9fa/1471-2164-11-S3-S16-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/2999346/588da63e21d5/1471-2164-11-S3-S16-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/322a/2999346/08cac0d430fe/1471-2164-11-S3-S16-4.jpg

相似文献

1
Investigation gene and microRNA expression in glioblastoma.研究脑胶质母细胞瘤的基因和 microRNA 表达。
BMC Genomics. 2010 Dec 1;11 Suppl 3(Suppl 3):S16. doi: 10.1186/1471-2164-11-S3-S16.
2
Computational analysis and verification of molecular genetic targets for glioblastoma.脑胶质母细胞瘤分子遗传学靶点的计算分析与验证。
Biosci Rep. 2020 Jun 26;40(6). doi: 10.1042/BSR20201401.
3
Simultaneous miRNA and mRNA transcriptome profiling of glioblastoma samples reveals a novel set of OncomiR candidates and their target genes.对胶质母细胞瘤样本进行 miRNA 和 mRNA 转录组同步分析,揭示了一组新的 OncomiR 候选物及其靶基因。
Brain Res. 2018 Dec 1;1700:199-210. doi: 10.1016/j.brainres.2018.08.035. Epub 2018 Aug 31.
4
PI3 kinase pathway regulated miRNome in glioblastoma: identification of miR-326 as a tumour suppressor miRNA.PI3激酶通路调控胶质母细胞瘤中的微小RNA组:鉴定miR-326为一种肿瘤抑制性微小RNA。
Mol Cancer. 2016 Nov 21;15(1):74. doi: 10.1186/s12943-016-0557-8.
5
Gene and microRNA Signatures Are Associated with the Development and Survival of Glioblastoma Patients.基因和 microRNA 特征与胶质母细胞瘤患者的发展和生存相关。
DNA Cell Biol. 2019 Jul;38(7):688-699. doi: 10.1089/dna.2018.4353. Epub 2019 Jun 12.
6
miRNAs as important drivers of glioblastomas: a no-brainer?miRNAs 作为胶质母细胞瘤的重要驱动因素:这是显而易见的吗?
Cancer Biomark. 2012;11(6):245-52. doi: 10.3233/CBM-2012-0271.
7
MicroRNA-300 inhibited glioblastoma progression through ROCK1.微小RNA-300通过ROCK1抑制胶质母细胞瘤进展。
Oncotarget. 2016 Jun 14;7(24):36529-36538. doi: 10.18632/oncotarget.9068.
8
Elucidating the microRNA-203 specific biological processes in glioblastoma cells from comprehensive RNA-sequencing transcriptome profiling.从综合 RNA 测序转录组图谱中阐明胶质母细胞瘤细胞中 microRNA-203 的特定生物学过程。
Cell Signal. 2019 Jan;53:22-38. doi: 10.1016/j.cellsig.2018.09.014. Epub 2018 Sep 20.
9
miR‑296‑3p promotes the proliferation of glioblastoma cells by targeting ICAT.miR-296-3p 通过靶向 ICAT 促进胶质母细胞瘤细胞的增殖。
Mol Med Rep. 2020 May;21(5):2151-2161. doi: 10.3892/mmr.2020.11011. Epub 2020 Mar 3.
10
The emerging role of tumor-suppressive microRNA-218 in targeting glioblastoma stemness.肿瘤抑制性微小RNA-218在靶向胶质母细胞瘤干性方面的新作用。
Cancer Lett. 2014 Oct 10;353(1):25-31. doi: 10.1016/j.canlet.2014.07.011. Epub 2014 Jul 17.

引用本文的文献

1
microRNAs (miRNAs) in Glioblastoma Multiforme (GBM)-Recent Literature Review.多形性胶质母细胞瘤(GBM)中的微小RNA(miRNA)——近期文献综述
Int J Mol Sci. 2023 Feb 9;24(4):3521. doi: 10.3390/ijms24043521.
2
Role of microRNAs in glioblastoma.微小RNA在胶质母细胞瘤中的作用。
Oncotarget. 2021 Aug 17;12(17):1707-1723. doi: 10.18632/oncotarget.28039.
3
Global expression of noncoding RNome reveals dysregulation of small RNAs in patients with HTLV-1-associated adult T-cell leukemia: a pilot study.非编码RNA组的整体表达揭示了HTLV-1相关成人T细胞白血病患者中小RNA的失调:一项初步研究。

本文引用的文献

1
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources.利用DAVID生物信息学资源对大型基因列表进行系统和综合分析。
Nat Protoc. 2009;4(1):44-57. doi: 10.1038/nprot.2008.211.
2
miR2Disease: a manually curated database for microRNA deregulation in human disease.miR2Disease:一个人工整理的关于人类疾病中 microRNA 失调的数据库。
Nucleic Acids Res. 2009 Jan;37(Database issue):D98-104. doi: 10.1093/nar/gkn714. Epub 2008 Oct 15.
3
MicroRNAs in cancer.癌症中的微小RNA
Infect Agent Cancer. 2021 Jan 9;16(1):4. doi: 10.1186/s13027-020-00343-2.
4
MiR-21, miR-34a, miR-125b, miR-181d and miR-648 levels inversely correlate with MGMT and TP53 expression in primary glioblastoma patients.在原发性胶质母细胞瘤患者中,miR-21、miR-34a、miR-125b、miR-181d和miR-648的水平与MGMT和TP53的表达呈负相关。
Arch Med Sci. 2019 Mar;15(2):504-512. doi: 10.5114/aoms.2017.69374. Epub 2017 Jul 31.
5
Genome-wide expression profiling of glioblastoma using a large combined cohort.使用大型联合队列对胶质母细胞瘤进行全基因组表达谱分析。
Sci Rep. 2018 Oct 10;8(1):15104. doi: 10.1038/s41598-018-33323-z.
6
Genome-Wide Sequencing Reveals Small Nucleolar RNAs Downregulated in Cerebral Cavernous Malformations.全基因组测序揭示脑静脉畸形中下调的小核仁 RNA。
Cell Mol Neurobiol. 2018 Oct;38(7):1369-1382. doi: 10.1007/s10571-018-0602-9. Epub 2018 Jul 10.
7
sPAGM: inferring subpathway activity by integrating gene and miRNA expression-robust functional signature identification for melanoma prognoses.sPAGM:通过整合基因和 miRNA 表达稳健的功能特征识别来推断亚通路活性,用于黑色素瘤预后。
Sci Rep. 2017 Nov 10;7(1):15322. doi: 10.1038/s41598-017-15631-y.
8
Genome-Wide Sequencing Reveals MicroRNAs Downregulated in Cerebral Cavernous Malformations.全基因组测序揭示脑海绵状血管畸形中下调的微小RNA
J Mol Neurosci. 2017 Feb;61(2):178-188. doi: 10.1007/s12031-017-0880-6. Epub 2017 Feb 8.
9
The Anti-Warburg Effect Elicited by the cAMP-PGC1α Pathway Drives Differentiation of Glioblastoma Cells into Astrocytes.cAMP-PGC1α 信号通路引发的抗瓦伯格效应驱动胶质母细胞瘤细胞向星形胶质细胞分化。
Cell Rep. 2017 Jan 10;18(2):468-481. doi: 10.1016/j.celrep.2016.12.037.
10
NOS Expression and NO Function in Glioma and Implications for Patient Therapies.胶质瘤中一氧化氮合酶的表达与一氧化氮功能及其对患者治疗的意义
Antioxid Redox Signal. 2017 Jun 10;26(17):986-999. doi: 10.1089/ars.2016.6820. Epub 2016 Aug 25.
Annu Rev Pathol. 2009;4:199-227. doi: 10.1146/annurev.pathol.4.110807.092222.
4
Comprehensive genomic characterization defines human glioblastoma genes and core pathways.全面的基因组特征分析确定了人类胶质母细胞瘤的基因和核心通路。
Nature. 2008 Oct 23;455(7216):1061-8. doi: 10.1038/nature07385. Epub 2008 Sep 4.
5
miR-124 and miR-137 inhibit proliferation of glioblastoma multiforme cells and induce differentiation of brain tumor stem cells.微小RNA-124和微小RNA-137抑制多形性胶质母细胞瘤细胞的增殖并诱导脑肿瘤干细胞分化。
BMC Med. 2008 Jun 24;6:14. doi: 10.1186/1741-7015-6-14.
6
Antagomir-17-5p abolishes the growth of therapy-resistant neuroblastoma through p21 and BIM.抗miR-17-5p通过p21和BIM抑制耐药性神经母细胞瘤的生长。
PLoS One. 2008 May 21;3(5):e2236. doi: 10.1371/journal.pone.0002236.
7
microRNA-7 inhibits the epidermal growth factor receptor and the Akt pathway and is down-regulated in glioblastoma.微小RNA-7抑制表皮生长因子受体和Akt信号通路,且在胶质母细胞瘤中表达下调。
Cancer Res. 2008 May 15;68(10):3566-72. doi: 10.1158/0008-5472.CAN-07-6639.
8
MicroRNA 29c is down-regulated in nasopharyngeal carcinomas, up-regulating mRNAs encoding extracellular matrix proteins.微小RNA 29c在鼻咽癌中表达下调,可上调编码细胞外基质蛋白的信使核糖核酸。
Proc Natl Acad Sci U S A. 2008 Apr 15;105(15):5874-8. doi: 10.1073/pnas.0801130105. Epub 2008 Apr 4.
9
MicroRNAs accurately identify cancer tissue origin.微小RNA能准确识别癌组织的起源。
Nat Biotechnol. 2008 Apr;26(4):462-9. doi: 10.1038/nbt1392. Epub 2008 Mar 23.
10
Experimental validation of miRNA targets.微小RNA(miRNA)靶标的实验验证
Methods. 2008 Jan;44(1):47-54. doi: 10.1016/j.ymeth.2007.09.005.