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HOXC8调节乳腺癌干细胞的自我更新、分化和转化。

HOXC8 regulates self-renewal, differentiation and transformation of breast cancer stem cells.

作者信息

Shah Mansi, Cardenas Ryan, Wang Belinda, Persson Jenny, Mongan Nigel P, Grabowska Anna, Allegrucci Cinzia

机构信息

SVMS, University of Nottingham, Sutton Bonington Campus, Loughborough, LE12 5RD, UK.

Department of Translational Medicine, Lund University, Malmö, 205 02, Sweden.

出版信息

Mol Cancer. 2017 Feb 16;16(1):38. doi: 10.1186/s12943-017-0605-z.

Abstract

BACKGROUND

Homeobox genes are master regulators of cell fate during embryonic development and their expression is altered in cancer. By regulating the balance between cell proliferation and differentiation, they maintain homeostasis of normal tissues. Here, we screened the expression of homeobox genes in mammary stem cells to establish their role in stem cells transformation in breast cancer.

METHODS

Using a Homeobox Genes PCR array, we screened 83 homeobox genes in normal cancer breast stem/progenitor cells isolated by flow cytometry. The candidate gene HOXC8 epigenetic regulation was studied by DNA methylation and miRNA expression analyses. Self-renewal and differentiation of HOXC8-overexpressing or knockdown cells were assessed by flow cytometry and mammosphere, 3D matrigel and soft agar assays. Clinical relevance of in vitro findings were validated by bioinformatics analysis of patient datasets from TCGA and METABRIC studies.

RESULTS

In this study we demonstrate altered expression of homeobox genes in breast cancer stem/progenitor cells. HOXC8 was consistently downregulated in stem/progenitor cells of all breast molecular subtypes, thus representing an interesting tumour suppressor candidate. We show that downregulated expression of HOXC8 is associated with DNA methylation at the gene promoter and expression of miR196 family members. Functional studies demonstrated that HOXC8 gain of function induces a decrease in the CD44/CD24 cancer stem cell population and proportion of chemoresistant cells, with a concomitant increase in CD24 differentiated cells. Increased HOXC8 levels also decrease the ability of cancer cells to form mammospheres and to grow in anchorage-independent conditions. Furthermore, loss of HOXC8 in non-tumorigenic mammary epithelial cells expands the cancer stem/progenitor cells pool, increases stem cell self-renewal, prevents differentiation induced by retinoic acid and induces a transformed phenotype.

CONCLUSIONS

Taken together, our study points to an important role of homeobox genes in breast cancer stem/progenitor cell function and establishes HOXC8 as a suppressor of stemness and transformation in the mammary gland lineage.

摘要

背景

同源框基因是胚胎发育过程中细胞命运的主要调节因子,其表达在癌症中会发生改变。通过调节细胞增殖与分化之间的平衡,它们维持正常组织的稳态。在此,我们筛选了同源框基因在乳腺干细胞中的表达,以确定它们在乳腺癌干细胞转化中的作用。

方法

使用同源框基因PCR阵列,我们筛选了通过流式细胞术分离的正常癌性乳腺干/祖细胞中的83个同源框基因。通过DNA甲基化和miRNA表达分析研究了候选基因HOXC8的表观遗传调控。通过流式细胞术、乳腺球、三维基质胶和软琼脂试验评估过表达或敲低HOXC8的细胞的自我更新和分化能力。通过对来自TCGA和METABRIC研究的患者数据集进行生物信息学分析,验证了体外研究结果的临床相关性。

结果

在本研究中,我们证明了同源框基因在乳腺癌干/祖细胞中的表达改变。HOXC8在所有乳腺分子亚型的干/祖细胞中均持续下调,因此是一个有趣的肿瘤抑制候选基因。我们表明,HOXC8表达下调与基因启动子处的DNA甲基化以及miR196家族成员的表达有关。功能研究表明,HOXC8功能获得会导致CD44/CD24癌症干细胞群体和化疗耐药细胞比例降低,同时CD24分化细胞增加。HOXC8水平升高还会降低癌细胞形成乳腺球和在非锚定依赖条件下生长的能力。此外,非致瘤性乳腺上皮细胞中HOXC8的缺失会扩大癌症干/祖细胞池,增加干细胞自我更新,阻止视黄酸诱导的分化并诱导转化表型。

结论

综上所述,我们的研究指出同源框基因在乳腺癌干/祖细胞功能中起重要作用,并将HOXC8确立为乳腺谱系中干性和转化的抑制因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22a5/5312582/723c2c20e9ea/12943_2017_605_Fig1_HTML.jpg

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