• 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

基于加权基因共表达网络分析鉴定嗜铬细胞瘤/副神经节瘤转移相关基因。

Identification of Genes Associated with the Metastasis of Pheochromocytoma/Paraganglioma Based on Weighted Gene Coexpression Network Analysis.

机构信息

Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region, China.

Department of Endocrinology, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region, China.

出版信息

Biomed Res Int. 2020 Feb 5;2020:3876834. doi: 10.1155/2020/3876834. eCollection 2020.

DOI:10.1155/2020/3876834
PMID:32090084
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7025031/
Abstract

BACKGROUND

Pheochromocytoma/paraganglioma (PCPG) is a benign neuroendocrine neoplasm in most cases, but metastasis and other malignant behaviors can be observed in this tumor. The aim of this study was to identify genes associated with the metastasis of PCPG.

METHODS

The Cancer Genome Atlas (TCGA) expression profile data and clinical information were downloaded from the cbioportal, and the weighted gene coexpression network analysis (WGCNA) was conducted. The gene coexpression modules were extracted from the network through the WGCNA package of R software. We further extracted metastasis-related modules of PCPG. Enrichment analysis of Biological Process of Gene Ontology and Kyoto Encyclopedia of Genes and Genomes was carried out for important modules, and survival analysis of hub genes in the modules was performed.

RESULTS

A total of 168 PCPG samples were included in this study. The weighted gene coexpression network was constructed with 5125 genes of the top 25% variance among the 20501 genes obtained from the database. We identified 11 coexpression modules, among which the salmon module was associated with the age of PCPG patients at diagnosis, metastasis, and malignancy of the tumors.

CONCLUSION

WGCNA was performed to identify the gene coexpression modules and hub genes in the metastasis-related gene module of PCPG. The findings in this study provide a new clue for further study of the mechanisms underlying the PCPG metastasis.

摘要

背景

嗜铬细胞瘤/副神经节瘤(PCPG)在大多数情况下是良性神经内分泌肿瘤,但在这种肿瘤中也可以观察到转移和其他恶性行为。本研究旨在鉴定与 PCPG 转移相关的基因。

方法

从 cbioportal 下载癌症基因组图谱(TCGA)表达谱数据和临床信息,并进行加权基因共表达网络分析(WGCNA)。通过 R 软件的 WGCNA 包从网络中提取基因共表达模块。我们进一步提取 PCPG 的转移相关模块。对重要模块进行基因本体论生物过程和京都基因与基因组百科全书的富集分析,并对模块中的枢纽基因进行生存分析。

结果

本研究共纳入 168 例 PCPG 样本。用数据库中 20501 个基因中前 25%方差的 5125 个基因构建加权基因共表达网络。我们鉴定出 11 个共表达模块,其中鲑鱼模块与 PCPG 患者诊断时的年龄、转移和肿瘤的恶性程度相关。

结论

通过 WGCNA 鉴定 PCPG 转移相关基因模块中的基因共表达模块和枢纽基因。本研究的结果为进一步研究 PCPG 转移的机制提供了新的线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4c5/7025031/abc874e44e6e/BMRI2020-3876834.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4c5/7025031/eab749003ce3/BMRI2020-3876834.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4c5/7025031/030c2034673f/BMRI2020-3876834.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4c5/7025031/c9022efefb7f/BMRI2020-3876834.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4c5/7025031/c0e692e7d088/BMRI2020-3876834.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4c5/7025031/abc874e44e6e/BMRI2020-3876834.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4c5/7025031/eab749003ce3/BMRI2020-3876834.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4c5/7025031/030c2034673f/BMRI2020-3876834.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4c5/7025031/c9022efefb7f/BMRI2020-3876834.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4c5/7025031/c0e692e7d088/BMRI2020-3876834.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4c5/7025031/abc874e44e6e/BMRI2020-3876834.005.jpg

相似文献

1
Identification of Genes Associated with the Metastasis of Pheochromocytoma/Paraganglioma Based on Weighted Gene Coexpression Network Analysis.基于加权基因共表达网络分析鉴定嗜铬细胞瘤/副神经节瘤转移相关基因。
Biomed Res Int. 2020 Feb 5;2020:3876834. doi: 10.1155/2020/3876834. eCollection 2020.
2
Identification of vital prognostic genes related to tumor microenvironment in pheochromocytoma and paraganglioma based on weighted gene co-expression network analysis.基于加权基因共表达网络分析鉴定嗜铬细胞瘤和副神经节瘤中与肿瘤微环境相关的关键预后基因。
Aging (Albany NY). 2021 Mar 26;13(7):9976-9990. doi: 10.18632/aging.202754.
3
Bioinformatic analysis of differentially expressed genes as prognostic markers in pheochromocytoma and paraganglioma tumors.生物信息学分析差异表达基因作为嗜铬细胞瘤和副神经节瘤肿瘤的预后标志物。
Genes Genet Syst. 2021 Jul 14;96(2):55-69. doi: 10.1266/ggs.20-00057. Epub 2021 May 26.
4
Long intergenic noncoding RNA profiles of pheochromocytoma and paraganglioma: A novel prognostic biomarker.嗜铬细胞瘤和副神经节瘤的长基因间非编码 RNA 谱:一种新的预后生物标志物。
Int J Cancer. 2020 Apr 15;146(8):2326-2335. doi: 10.1002/ijc.32654. Epub 2019 Oct 11.
5
Clinicopathological characteristics of pheochromocytoma/paraganglioma and screening of prognostic markers.嗜铬细胞瘤/副神经节瘤的临床病理特征和预后标志物的筛选。
J Surg Oncol. 2023 Sep;128(4):510-518. doi: 10.1002/jso.27358. Epub 2023 Jun 5.
6
Transcriptome-guided resolution of tumor microenvironment interactions in pheochromocytoma and paraganglioma subtypes.基于转录组学解析嗜铬细胞瘤和副神经节瘤亚型中的肿瘤微环境相互作用。
J Endocrinol Invest. 2022 May;45(5):989-998. doi: 10.1007/s40618-021-01729-8. Epub 2022 Jan 28.
7
Single-nuclei and bulk-tissue gene-expression analysis of pheochromocytoma and paraganglioma links disease subtypes with tumor microenvironment.对嗜铬细胞瘤和副神经节瘤的单细胞和组织基因表达分析将疾病亚型与肿瘤微环境联系起来。
Nat Commun. 2022 Oct 21;13(1):6262. doi: 10.1038/s41467-022-34011-3.
8
Identification of vital modules and genes associated with heart failure based on weighted gene coexpression network analysis.基于加权基因共表达网络分析鉴定与心力衰竭相关的关键模块和基因。
ESC Heart Fail. 2022 Apr;9(2):1370-1379. doi: 10.1002/ehf2.13827. Epub 2022 Feb 6.
9
Identification of critical genes associated with human osteosarcoma metastasis based on integrated gene expression profiling.基于基因表达谱整合分析鉴定与人类骨肉瘤转移相关的关键基因。
Mol Med Rep. 2019 Aug;20(2):915-930. doi: 10.3892/mmr.2019.10323. Epub 2019 Jun 3.
10
Identification of specific modules and significant genes associated with colon cancer by weighted gene co‑expression network analysis.通过加权基因共表达网络分析鉴定与结肠癌相关的特定模块和显著基因。
Mol Med Rep. 2019 Jul;20(1):693-700. doi: 10.3892/mmr.2019.10295. Epub 2019 May 24.

引用本文的文献

1
TOP2A Expression in Pheochromocytoma and Abdominal Paraganglioma: a Marker of Poor Clinical Outcome?TOP2A 在嗜铬细胞瘤和腹腔嗜铬细胞瘤中的表达:临床预后不良的标志物?
Endocr Pathol. 2023 Mar;34(1):129-141. doi: 10.1007/s12022-022-09746-w. Epub 2023 Jan 19.
2
Identification of vital prognostic genes related to tumor microenvironment in pheochromocytoma and paraganglioma based on weighted gene co-expression network analysis.基于加权基因共表达网络分析鉴定嗜铬细胞瘤和副神经节瘤中与肿瘤微环境相关的关键预后基因。
Aging (Albany NY). 2021 Mar 26;13(7):9976-9990. doi: 10.18632/aging.202754.
3
The Potential of Five Immune-Related Prognostic Genes to Predict Survival and Response to Immune Checkpoint Inhibitors for Soft Tissue Sarcomas Based on Multi-Omic Study.

本文引用的文献

1
A Novel Intergenic Region between CENPA and DPYSL5-ALK Exon 20 Fusion Variant Responding to Crizotinib Treatment in a Patient with Lung Adenocarcinoma.在一名肺腺癌患者中,CENPA与DPYSL5-ALK外显子20融合变体之间的一个新型基因间区域对克唑替尼治疗有反应。
J Thorac Oncol. 2019 Sep;14(9):e191-e193. doi: 10.1016/j.jtho.2019.04.012.
2
Glycemic Disturbances in Pheochromocytoma and Paraganglioma.嗜铬细胞瘤和副神经节瘤中的血糖紊乱
Cureus. 2019 Apr 27;11(4):e4551. doi: 10.7759/cureus.4551.
3
Master regulator analysis of paragangliomas carrying SDHx, VHL, or MAML3 genetic alterations.
基于多组学研究的五个免疫相关预后基因预测软组织肉瘤生存及对免疫检查点抑制剂反应的潜力
Front Oncol. 2020 Jul 24;10:1317. doi: 10.3389/fonc.2020.01317. eCollection 2020.
带有 SDHx、VHL 或 MAML3 基因突变的副神经节瘤的主调控因子分析。
BMC Cancer. 2019 Jun 24;19(1):619. doi: 10.1186/s12885-019-5813-z.
4
Epigenetic Deregulation of Protocadherin PCDHGC3 in Pheochromocytomas/Paragangliomas Associated With SDHB Mutations.SDHB 突变相关嗜铬细胞瘤/副神经节瘤中原钙黏蛋白 PCDHGC3 的表观遗传失调。
J Clin Endocrinol Metab. 2019 Nov 1;104(11):5673-5692. doi: 10.1210/jc.2018-01471.
5
WebGestalt 2019: gene set analysis toolkit with revamped UIs and APIs.WebGestalt 2019:基因集分析工具包,具有全新的用户界面和 API。
Nucleic Acids Res. 2019 Jul 2;47(W1):W199-W205. doi: 10.1093/nar/gkz401.
6
Up-regulation of CKAP2L expression promotes lung adenocarcinoma invasion and is associated with poor prognosis.CKAP2L表达上调促进肺腺癌侵袭并与不良预后相关。
Onco Targets Ther. 2019 Feb 12;12:1171-1180. doi: 10.2147/OTT.S182242. eCollection 2019.
7
Molecular Profiling of Pheochromocytoma and Abdominal Paraganglioma Stratified by the PASS Algorithm Reveals Chromogranin B as Associated With Histologic Prediction of Malignant Behavior.采用 PASS 算法对嗜铬细胞瘤和腹腔嗜铬细胞瘤进行分子谱分析,结果显示嗜铬粒蛋白 B 与组织学恶性行为预测相关。
Am J Surg Pathol. 2019 Mar;43(3):409-421. doi: 10.1097/PAS.0000000000001190.
8
Germline SDHB and SDHD mutations in pheochromocytoma and paraganglioma patients.嗜铬细胞瘤和副神经节瘤患者的种系SDHB和SDHD突变
Endocr Connect. 2018 Dec 1;7(12):1217-1225. doi: 10.1530/EC-18-0325.
9
CKAP2L mutation confirms the diagnosis of Filippi syndrome.CKAP2L基因突变确诊了菲利皮综合征。
Clin Genet. 2018 May;93(5):1109-1110. doi: 10.1111/cge.13188. Epub 2018 Feb 23.
10
Targeting dual specificity protein kinase TTK attenuates tumorigenesis of glioblastoma.靶向双特异性蛋白激酶TTK可减弱胶质母细胞瘤的肿瘤发生。
Oncotarget. 2017 Dec 11;9(3):3081-3088. doi: 10.18632/oncotarget.23152. eCollection 2018 Jan 9.