• 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

MGDB:一个与黑色素瘤相关基因的综合数据库。

MGDB: a comprehensive database of genes involved in melanoma.

作者信息

Zhang Di, Zhu Rongrong, Zhang Hanqian, Zheng Chun-Hou, Xia Junfeng

机构信息

Institute of Health Sciences, School of Computer Science and Technology.

College of Electrical Engineering and Automation and Center of Information Support and Assurance Technology, Anhui University, Hefei, Anhui 230601, China.

出版信息

Database (Oxford). 2015 Sep 30;2015. doi: 10.1093/database/bav097. Print 2015.

DOI:10.1093/database/bav097
PMID:26424083
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4589692/
Abstract

The Melanoma Gene Database (MGDB) is a manually curated catalog of molecular genetic data relating to genes involved in melanoma. The main purpose of this database is to establish a network of melanoma related genes and to facilitate the mechanistic study of melanoma tumorigenesis. The entries describing the relationships between melanoma and genes in the current release were manually extracted from PubMed abstracts, which contains cumulative to date 527 human melanoma genes (422 protein-coding and 105 non-coding genes). Each melanoma gene was annotated in seven different aspects (General Information, Expression, Methylation, Mutation, Interaction, Pathway and Drug). In addition, manually curated literature references have also been provided to support the inclusion of the gene in MGDB and establish its association with melanoma. MGDB has a user-friendly web interface with multiple browse and search functions. We hoped MGDB will enrich our knowledge about melanoma genetics and serve as a useful complement to the existing public resources. Database URL: http://bioinfo.ahu.edu.cn:8080/Melanoma/index.jsp.

摘要

黑色素瘤基因数据库(MGDB)是一个人工整理的、与黑色素瘤相关基因的分子遗传数据目录。该数据库的主要目的是建立一个黑色素瘤相关基因网络,并促进黑色素瘤肿瘤发生的机制研究。当前版本中描述黑色素瘤与基因之间关系的条目是从PubMed摘要中手动提取的,截至目前共包含527个人类黑色素瘤基因(422个蛋白质编码基因和105个非编码基因)。每个黑色素瘤基因都从七个不同方面进行了注释(一般信息、表达、甲基化、突变、相互作用、通路和药物)。此外,还提供了人工整理的文献参考资料,以支持该基因被纳入MGDB并确立其与黑色素瘤的关联。MGDB拥有一个用户友好的网络界面,具备多种浏览和搜索功能。我们希望MGDB能丰富我们对黑色素瘤遗传学的认识,并作为现有公共资源的有益补充。数据库网址:http://bioinfo.ahu.edu.cn:8080/Melanoma/index.jsp。

相似文献

1
MGDB: a comprehensive database of genes involved in melanoma.MGDB:一个与黑色素瘤相关基因的综合数据库。
Database (Oxford). 2015 Sep 30;2015. doi: 10.1093/database/bav097. Print 2015.
2
An annotated dataset for extracting gene-melanoma relations from scientific literature.从科学文献中提取基因-黑色素瘤关系的带注释数据集。
J Biomed Semantics. 2022 Jan 19;13(1):2. doi: 10.1186/s13326-021-00251-3.
3
dbCPG: A web resource for cancer predisposition genes.dbCPG:癌症易感基因的网络资源。
Oncotarget. 2016 Jun 21;7(25):37803-37811. doi: 10.18632/oncotarget.9334.
4
CCDB: a curated database of genes involved in cervix cancer.CCDB:一个精心策划的宫颈癌相关基因数据库。
Nucleic Acids Res. 2011 Jan;39(Database issue):D975-9. doi: 10.1093/nar/gkq1024. Epub 2010 Nov 2.
5
dbDSM: a manually curated database for deleterious synonymous mutations.dbDSM:一个经过人工整理的有害同义突变数据库。
Bioinformatics. 2016 Jun 15;32(12):1914-6. doi: 10.1093/bioinformatics/btw086. Epub 2016 Feb 15.
6
PGDB: a curated and integrated database of genes related to the prostate.前列腺基因数据库(PGDB):一个经过整理和整合的与前列腺相关基因的数据库。
Nucleic Acids Res. 2003 Jan 1;31(1):291-3. doi: 10.1093/nar/gkg008.
7
CancerProView: a graphical image database of cancer-related genes and proteins.CancerProView:一个与癌症相关基因和蛋白质的图形图像数据库。
Genomics. 2012 Aug;100(2):81-92. doi: 10.1016/j.ygeno.2012.05.011. Epub 2012 May 31.
8
ATID: a web-oriented database for collection of publicly available alternative translational initiation events.ATID:一个面向网络的数据库,用于收集公开可用的替代性翻译起始事件。
Bioinformatics. 2005 Dec 1;21(23):4312-4. doi: 10.1093/bioinformatics/bti704. Epub 2005 Oct 10.
9
ITTACA: a new database for integrated tumor transcriptome array and clinical data analysis.ITTACA:一个用于整合肿瘤转录组阵列和临床数据分析的新数据库。
Nucleic Acids Res. 2006 Jan 1;34(Database issue):D613-6. doi: 10.1093/nar/gkj022.
10
dbRES: a web-oriented database for annotated RNA editing sites.dbRES:一个面向网络的注释RNA编辑位点数据库。
Nucleic Acids Res. 2007 Jan;35(Database issue):D141-4. doi: 10.1093/nar/gkl815. Epub 2006 Nov 6.

引用本文的文献

1
Multiplexed single-cell transcriptomics reveals diverse phenotypic outcomes for pathogenic SHP2 variants.多重单细胞转录组学揭示了致病性SHP2变体的多种表型结果。
bioRxiv. 2025 Jul 2:2025.06.30.662374. doi: 10.1101/2025.06.30.662374.
2
Links between melanoma germline risk loci, driver genes and comorbidities: insight from a tissue-specific multi-omic analysis.黑色素瘤种系风险位点、驱动基因与合并症之间的关联:来自组织特异性多组学分析的见解。
Mol Oncol. 2024 Apr;18(4):1031-1048. doi: 10.1002/1878-0261.13599. Epub 2024 Feb 3.
3
S-adenosylmethionine blocks tumorigenesis and with immune checkpoint inhibitor enhances anti-cancer efficacy against BRAF mutant and wildtype melanomas.

本文引用的文献

1
Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012.全球癌症发病与死亡:GLOBOCAN 2012 数据源、方法与主要模式。
Int J Cancer. 2015 Mar 1;136(5):E359-86. doi: 10.1002/ijc.29210. Epub 2014 Oct 9.
2
A meta-analysis of somatic mutations from next generation sequencing of 241 melanomas: a road map for the study of genes with potential clinical relevance.对241例黑色素瘤二代测序的体细胞突变进行的荟萃分析:具有潜在临床相关性基因研究的路线图。
Mol Cancer Ther. 2014 Jul;13(7):1918-28. doi: 10.1158/1535-7163.MCT-13-0804. Epub 2014 Apr 22.
3
Novel downstream molecular targets of SIRT1 in melanoma: a quantitative proteomics approach.
S-腺苷甲硫氨酸阻断肿瘤发生,并与免疫检查点抑制剂联合增强对 BRAF 突变型和野生型黑色素瘤的抗癌疗效。
Neoplasia. 2023 Feb;36:100874. doi: 10.1016/j.neo.2022.100874. Epub 2023 Jan 11.
4
An annotated dataset for extracting gene-melanoma relations from scientific literature.从科学文献中提取基因-黑色素瘤关系的带注释数据集。
J Biomed Semantics. 2022 Jan 19;13(1):2. doi: 10.1186/s13326-021-00251-3.
5
ILDGDB: a manually curated database of genomics, transcriptomics, proteomics and drug information for interstitial lung diseases.ILDGDB:一个经过人工整理的基因组学、转录组学、蛋白质组学和药物信息数据库,用于间质性肺疾病。
BMC Pulm Med. 2020 Dec 11;20(1):323. doi: 10.1186/s12890-020-01350-0.
6
Enhanced Anticancer Effect of a Combination of S-adenosylmethionine (SAM) and Immune Checkpoint Inhibitor (ICPi) in a Syngeneic Mouse Model of Advanced Melanoma.S-腺苷甲硫氨酸(SAM)与免疫检查点抑制剂(ICPi)联合使用在晚期黑色素瘤同基因小鼠模型中的抗癌效果增强
Front Oncol. 2020 Sep 2;10:1361. doi: 10.3389/fonc.2020.01361. eCollection 2020.
7
Computational models of melanoma.黑色素瘤的计算模型。
Theor Biol Med Model. 2020 May 14;17(1):8. doi: 10.1186/s12976-020-00126-7.
8
Transcriptome analysis of dog oral melanoma and its oncogenic analogy with human melanoma.狗口腔黑色素瘤的转录组分析及其与人类黑色素瘤的致癌类比。
Oncol Rep. 2020 Jan;43(1):16-30. doi: 10.3892/or.2019.7391. Epub 2019 Oct 25.
黑色素瘤中SIRT1的新型下游分子靶点:一种定量蛋白质组学方法。
Oncotarget. 2014 Apr 15;5(7):1987-99. doi: 10.18632/oncotarget.1898.
4
miRTarBase update 2014: an information resource for experimentally validated miRNA-target interactions.miRTarBase 更新 2014:一个经过实验验证的 miRNA 靶标相互作用的信息资源。
Nucleic Acids Res. 2014 Jan;42(Database issue):D78-85. doi: 10.1093/nar/gkt1266. Epub 2013 Dec 4.
5
DGIdb: mining the druggable genome.DGIdb:挖掘可成药的基因组。
Nat Methods. 2013 Dec;10(12):1209-10. doi: 10.1038/nmeth.2689. Epub 2013 Oct 13.
6
Epigenome-wide DNA methylation landscape of melanoma progression to brain metastasis reveals aberrations on homeobox D cluster associated with prognosis.黑色素瘤进展至脑转移的全基因组DNA甲基化图谱揭示了与预后相关的同源框D簇异常。
Hum Mol Genet. 2014 Jan 1;23(1):226-38. doi: 10.1093/hmg/ddt420. Epub 2013 Sep 6.
7
A landscape of driver mutations in melanoma.黑色素瘤中的驱动基因突变全景。
Cell. 2012 Jul 20;150(2):251-63. doi: 10.1016/j.cell.2012.06.024.
8
BRAF(L597) mutations in melanoma are associated with sensitivity to MEK inhibitors.黑色素瘤中的 BRAF(L597) 突变与对 MEK 抑制剂的敏感性相关。
Cancer Discov. 2012 Sep;2(9):791-7. doi: 10.1158/2159-8290.CD-12-0097. Epub 2012 Jul 13.
9
RCDB: Renal Cancer Gene Database.RCDB:肾癌基因数据库。
BMC Res Notes. 2012 May 18;5:246. doi: 10.1186/1756-0500-5-246.
10
Routine multiplex mutational profiling of melanomas enables enrollment in genotype-driven therapeutic trials.对黑色素瘤进行常规多重突变分析可使患者入组到基于基因分型的治疗试验中。
PLoS One. 2012;7(4):e35309. doi: 10.1371/journal.pone.0035309. Epub 2012 Apr 20.