Suppr超能文献

微阵列数据集的荟萃分析确定了几个与染色体分离相关的癌胚基因,它们可能与间变性甲状腺癌的发生有关。

Meta-analysis of microarray datasets identify several chromosome segregation-related cancer/testis genes potentially contributing to anaplastic thyroid carcinoma.

作者信息

Liu Mu, Qiu Yu-Lu, Jin Tong, Zhou Yin, Mao Zhi-Yuan, Zhang Yong-Jie

机构信息

The First Medical School of Nanjing Medical University, Nanjing Medical University, Nanjing, Jiangsu, China.

School of Basic Medical Sciences, Nanjing Medical University, Nanjing, Jiangsu, China.

出版信息

PeerJ. 2018 Oct 24;6:e5822. doi: 10.7717/peerj.5822. eCollection 2018.

Abstract

AIM

Anaplastic thyroid carcinoma (ATC) is the most lethal thyroid malignancy. Identification of novel drug targets is urgently needed.

MATERIALS & METHODS: We re-analyzed several GEO datasets by systematic retrieval and data merging. Differentially expressed genes (DEGs) were filtered out. We also performed pathway enrichment analysis to interpret the data. We predicted key genes based on protein-protein interaction networks, weighted gene co-expression network analysis and genes' cancer/testis expression pattern. We also further characterized these genes using data from the Cancer Genome Atlas (TCGA) project and gene ontology annotation.

RESULTS

Cell cycle-related pathways were significantly enriched in upregulated genes in ATC. We identified , , , , , , , , and as cell cycle-related key genes with cancer/testis expression pattern. We further uncovered that most of these putative key genes were critical components during chromosome segregation.

CONCLUSION

We predicted several key genes harboring potential therapeutic value in ATC. Cell cycle-related processes, especially chromosome segregation, may be the key to tumorigenesis and treatment of ATC.

摘要

目的

间变性甲状腺癌(ATC)是最致命的甲状腺恶性肿瘤。迫切需要鉴定新的药物靶点。

材料与方法

我们通过系统检索和数据合并对多个基因表达综合数据库(GEO)数据集进行了重新分析。筛选出差异表达基因(DEG)。我们还进行了通路富集分析以解释数据。我们基于蛋白质-蛋白质相互作用网络、加权基因共表达网络分析和基因的癌/睾丸表达模式预测关键基因。我们还使用来自癌症基因组图谱(TCGA)项目的数据和基因本体注释对这些基因进行了进一步表征。

结果

细胞周期相关通路在ATC上调基因中显著富集。我们鉴定出 、 、 、 、 、 、 、 和 为具有癌/睾丸表达模式的细胞周期相关关键基因。我们进一步发现这些推定的关键基因中的大多数是染色体分离过程中的关键成分。

结论

我们预测了几个在ATC中具有潜在治疗价值的关键基因。细胞周期相关过程,尤其是染色体分离,可能是ATC肿瘤发生和治疗的关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18b0/6203939/74015b277beb/peerj-06-5822-g001.jpg

相似文献

4
Identification of Hub Genes in Anaplastic Thyroid Carcinoma: Evidence From Bioinformatics Analysis.
Technol Cancer Res Treat. 2020 Jan-Dec;19:1533033820962135. doi: 10.1177/1533033820962135.
5
Identification and Validation of Novel Genes in Anaplastic Thyroid Carcinoma via Bioinformatics Analysis.
Cancer Manag Res. 2020 Oct 8;12:9787-9799. doi: 10.2147/CMAR.S250792. eCollection 2020.
7
Cell Cycle M-Phase Genes Are Highly Upregulated in Anaplastic Thyroid Carcinoma.
Thyroid. 2017 Feb;27(2):236-252. doi: 10.1089/thy.2016.0285. Epub 2016 Dec 15.
8
Integrated Bioinformatics Analysis of Hub Genes and Pathways in Anaplastic Thyroid Carcinomas.
Int J Endocrinol. 2019 Jan 13;2019:9651380. doi: 10.1155/2019/9651380. eCollection 2019.
9
[Identification of key pathways and drug repurposing for anaplastic thyroid carcinoma by integrated bioinformatics analysis].
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2018 May 25;47(2):187-193. doi: 10.3785/j.issn.1008-9292.2018.04.13.
10
Identification of hub genes associated with bladder cancer using bioinformatic analyses.
Transl Cancer Res. 2022 May;11(5):1330-1343. doi: 10.21037/tcr-22-1004.

引用本文的文献

3
Ectopic expression of meiotic cohesin generates chromosome instability in cancer cell line.
Proc Natl Acad Sci U S A. 2022 Oct 4;119(40):e2204071119. doi: 10.1073/pnas.2204071119. Epub 2022 Sep 30.
6
Identification and Validation of Novel Genes in Anaplastic Thyroid Carcinoma via Bioinformatics Analysis.
Cancer Manag Res. 2020 Oct 8;12:9787-9799. doi: 10.2147/CMAR.S250792. eCollection 2020.
7
TRIP13 predicts poor prognosis in clear cell renal cell carcinoma.
Am J Cancer Res. 2020 Sep 1;10(9):2909-2918. eCollection 2020.
8
Overexpression of mRNA in head and neck carcinoma and association with response to vinorelbine.
Oncol Lett. 2020 Mar;19(3):2502-2507. doi: 10.3892/ol.2020.11339. Epub 2020 Jan 23.
9
Identification of five hub genes as monitoring biomarkers for breast cancer metastasis in silico.
Hereditas. 2019 Jun 21;156:20. doi: 10.1186/s41065-019-0096-6. eCollection 2019.

本文引用的文献

1
Mechanism for remodelling of the cell cycle checkpoint protein MAD2 by the ATPase TRIP13.
Nature. 2018 Jul;559(7713):274-278. doi: 10.1038/s41586-018-0281-1. Epub 2018 Jul 4.
2
Massive mining of publicly available RNA-seq data from human and mouse.
Nat Commun. 2018 Apr 10;9(1):1366. doi: 10.1038/s41467-018-03751-6.
3
Thyroid hormone receptor interactor 13 (TRIP13) overexpression associated with tumor progression and poor prognosis in lung adenocarcinoma.
Biochem Biophys Res Commun. 2018 May 15;499(3):416-424. doi: 10.1016/j.bbrc.2018.03.129. Epub 2018 Mar 30.
4
TRIP13 promotes tumor growth and is associated with poor prognosis in colorectal cancer.
Cell Death Dis. 2018 Mar 14;9(3):402. doi: 10.1038/s41419-018-0434-z.
5
Anaplastic thyroid carcinoma: review of treatment protocols.
Endocr Relat Cancer. 2018 Mar;25(3):R153-R161. doi: 10.1530/ERC-17-0435. Epub 2018 Jan 2.
6
Real-World Experience with Targeted Therapy for the Treatment of Anaplastic Thyroid Carcinoma.
Thyroid. 2018 Jan;28(1):79-87. doi: 10.1089/thy.2017.0285. Epub 2017 Dec 21.
7
Dabrafenib and Trametinib Treatment in Patients With Locally Advanced or Metastatic BRAF V600-Mutant Anaplastic Thyroid Cancer.
J Clin Oncol. 2018 Jan 1;36(1):7-13. doi: 10.1200/JCO.2017.73.6785. Epub 2017 Oct 26.
9
Anaplastic thyroid carcinoma: from clinicopathology to genetics and advanced therapies.
Nat Rev Endocrinol. 2017 Nov;13(11):644-660. doi: 10.1038/nrendo.2017.76. Epub 2017 Jul 14.
10
Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation.
Nat Genet. 2017 Jul;49(7):1148-1151. doi: 10.1038/ng.3883. Epub 2017 May 29.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验