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钙黏蛋白与不同的干细胞相关转录因子结合,以协调三阴性乳腺癌干性的维持。

Cadherins Associate with Distinct Stem Cell-Related Transcription Factors to Coordinate the Maintenance of Stemness in Triple-Negative Breast Cancer.

作者信息

Yang Chuanwei, Zhao Xuemei, Cui Naipeng, Liang Yulong

机构信息

Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

College of Pharmacy, Taishan Medical University, Tai'an, Shandong, China.

出版信息

Stem Cells Int. 2017;2017:5091541. doi: 10.1155/2017/5091541. Epub 2017 Mar 14.

DOI:10.1155/2017/5091541
PMID:28392805
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5368378/
Abstract

Triple-negative breast cancer (TNBC) is an aggressive type of breast cancer with poor prognosis and is enriched in cancer stem cells (CSCs). However, it is not completely understood how the CSCs were maintained in TNBC. In this study, by analyzing The Cancer Genome Atlas (TCGA) provisional datasets and several small-size breast datasets, we found that cadherins (CDHs) 2, 4, 6, and 17 were frequently amplified/overexpressed in 47% of TNBC while E-cadherin (CDH1) was downregulated/mutated at 10%. The alterations of CDH2/4/6/17 were strongly associated with the elevated levels of several stem cell-related transcription factors (SC-TFs) including FOXM1, MCM2, WWTR1, SNAI1, and SOX9. CDH2/4/6/17-enriched genes including FOXM1 and MCM2 were also clustered and regulated by NFY (nuclear transcription factor Y) and/or EVI1/MECOM. Meanwhile, these SC-TFs including NFYA were upregulated in TNBC cells, but they were downregulated in luminal type of cells. Furthermore, small compounds might be predicted via the Connectivity Map analysis to target TNBC with the alterations of CDH2/4/6/17 and SC-TFs. Together with the important role of these SC-TFs in the stem cell regulation, our data provide novel insights into the maintenance of CSCs in TNBC and the discovery of these SC-TFs associated with the alterations of CDH2/4/6/17 has an implication in targeted therapy of TNBC.

摘要

三阴性乳腺癌(TNBC)是一种侵袭性乳腺癌,预后较差,且富含癌症干细胞(CSC)。然而,目前尚不完全清楚TNBC中的CSC是如何维持的。在本研究中,通过分析癌症基因组图谱(TCGA)临时数据集和几个小样本乳腺癌数据集,我们发现钙黏蛋白(CDH)2、4、6和17在47%的TNBC中频繁扩增/过表达,而E-钙黏蛋白(CDH1)在10%的病例中下调/突变。CDH2/4/6/17的改变与几种干细胞相关转录因子(SC-TF)水平升高密切相关,这些转录因子包括叉头框蛋白M1(FOXM1)、微小染色体维持蛋白2(MCM2)、WW转录调节因子1(WWTR1)、Snail家族转录抑制因子1(SNAI1)和性别决定区Y盒9(SOX9)。包括FOXM1和MCM2在内的富含CDH2/4/6/17的基因也由核转录因子Y(NFY)和/或EVI1/MECOM聚类和调控。同时,包括NFYA在内的这些SC-TF在TNBC细胞中上调,但在管腔型细胞中下调。此外,通过连通性图谱分析可能预测出小分子化合物,以靶向具有CDH2/4/6/17和SC-TF改变的TNBC。鉴于这些SC-TF在干细胞调节中的重要作用,我们的数据为TNBC中CSC的维持提供了新的见解,并且发现这些与CDH2/4/6/17改变相关的SC-TF对TNBC的靶向治疗具有重要意义。

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