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功能基因组时代的乳腺癌生物标志物发现:对42种基因表达特征的系统综述

Breast cancer biomarker discovery in the functional genomic age: a systematic review of 42 gene expression signatures.

作者信息

Abba M C, Lacunza E, Butti M, Aldaz C M

机构信息

Centro de Investigaciones Inmunológicas Básicas y Aplicadas (CINIBA), Facultad de Ciencias Médicas, Universidad Nacional de La Plata, Argentina.

出版信息

Biomark Insights. 2010 Oct 27;5:103-18. doi: 10.4137/BMI.S5740.

DOI:10.4137/BMI.S5740
PMID:21082037
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2978930/
Abstract

In this review we provide a systematic analysis of transcriptomic signatures derived from 42 breast cancer gene expression studies, in an effort to identify the most relevant breast cancer biomarkers using a meta-analysis method. Meta-data revealed a set of 117 genes that were the most commonly affected ranging from 12% to 36% of overlap among breast cancer gene expression studies. Data mining analysis of transcripts and protein-protein interactions of these commonly modulated genes indicate three functional modules significantly affected among signatures, one module related with the response to steroid hormone stimulus, and two modules related to the cell cycle. Analysis of a publicly available gene expression data showed that the obtained meta-signature is capable of predicting overall survival (P < 0.0001) and relapse-free survival (P < 0.0001) in patients with early-stage breast carcinomas. In addition, the identified meta-signature improves breast cancer patient stratification independently of traditional prognostic factors in a multivariate Cox proportional-hazards analysis.

摘要

在本综述中,我们对来自42项乳腺癌基因表达研究的转录组特征进行了系统分析,旨在使用荟萃分析方法识别最相关的乳腺癌生物标志物。元数据揭示了一组117个基因,这些基因在乳腺癌基因表达研究中的重叠率最常受到影响,范围从12%到36%。对这些常见调控基因的转录本和蛋白质-蛋白质相互作用进行数据挖掘分析表明,在特征中三个功能模块受到显著影响,一个模块与对类固醇激素刺激的反应相关,另外两个模块与细胞周期相关。对公开可用的基因表达数据的分析表明,所获得的元特征能够预测早期乳腺癌患者的总生存期(P < 0.0001)和无复发生存期(P < 0.0001)。此外,在多变量Cox比例风险分析中,所识别的元特征独立于传统预后因素改善了乳腺癌患者的分层。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/2978930/8f070b448b07/bmi-2010-103f5a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/2978930/ca6f9db0d3ab/bmi-2010-103f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/2978930/57c56ddb26cc/bmi-2010-103f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/2978930/5359514ca7a4/bmi-2010-103f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/2978930/a27ccbe4767c/bmi-2010-103f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/2978930/8f070b448b07/bmi-2010-103f5a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/2978930/ca6f9db0d3ab/bmi-2010-103f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/2978930/57c56ddb26cc/bmi-2010-103f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/2978930/5359514ca7a4/bmi-2010-103f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/2978930/a27ccbe4767c/bmi-2010-103f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/2978930/8f070b448b07/bmi-2010-103f5a.jpg

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1
Polo-like kinase inhibitors: an emerging opportunity for cancer therapeutics.Polo-like 激酶抑制剂:癌症治疗的新兴机会。
Expert Opin Investig Drugs. 2010 Jan;19(1):27-43. doi: 10.1517/13543780903483191.
2
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Nucleic Acids Res. 2010 Jan;38(Database issue):D716-25. doi: 10.1093/nar/gkp1015. Epub 2009 Nov 24.
3
Centromere assembly requires the direct recognition of CENP-A nucleosomes by CENP-N.着丝粒组装需要CENP-N直接识别CENP-A核小体。
NAT1 通过调控 EMT 和糖酵解抑制结直肠癌肝转移。
Aging (Albany NY). 2024 Jun 24;16(12):10546-10562. doi: 10.18632/aging.205957.
4
The Transcriptomic Portrait of Locally Advanced Breast Cancer and Its Prognostic Value in a Multi-Country Cohort of Latin American Patients.拉丁美洲患者多国队列中局部晚期乳腺癌的转录组图谱及其预后价值
Front Oncol. 2022 Mar 22;12:835626. doi: 10.3389/fonc.2022.835626. eCollection 2022.
5
Computational analysis of fused co-expression networks for the identification of candidate cancer gene biomarkers.基于融合共表达网络的计算分析鉴定候选癌症基因生物标志物。
NPJ Syst Biol Appl. 2021 Mar 12;7(1):17. doi: 10.1038/s41540-021-00175-9.
6
Prognostic gene expression signatures of breast cancer are lacking a sensible biological meaning.乳腺癌预后基因表达特征缺乏合理的生物学意义。
Sci Rep. 2021 Jan 8;11(1):156. doi: 10.1038/s41598-020-79375-y.
7
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Card Fail Rev. 2020 Sep 28;6:e24. doi: 10.15420/cfr.2019.19. eCollection 2020 Mar.
8
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J Cancer Res Clin Oncol. 2019 May;145(5):1283-1295. doi: 10.1007/s00432-019-02897-0. Epub 2019 Mar 21.
9
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J Mol Med (Berl). 2019 Apr;97(4):491-508. doi: 10.1007/s00109-019-01750-8. Epub 2019 Feb 7.
10
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J Neurooncol. 2019 Jan;141(1):57-70. doi: 10.1007/s11060-018-03029-3. Epub 2018 Nov 9.
Nat Cell Biol. 2009 Jul;11(7):896-902. doi: 10.1038/ncb1899. Epub 2009 Jun 21.
4
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5
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6
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Nat Cell Biol. 2008 Sep;10(9):1076-82. doi: 10.1038/ncb1767.
7
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10
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