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CHD4/NuRD 复合物调节补体基因表达,并与人肝癌中 CD8 T 细胞浸润相关。

CHD4/NuRD complex regulates complement gene expression and correlates with CD8 T cell infiltration in human hepatocellular carcinoma.

机构信息

Jiangsu Key Laboratory of Brain Disease and Bioinformation, Research Center for Biochemistry and Molecular Biology, Xuzhou Medical University, Xuzhou, China.

Department of Endocrinology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, China.

出版信息

Clin Epigenetics. 2020 Feb 18;12(1):31. doi: 10.1186/s13148-020-00827-3.

Abstract

BACKGROUNDS

The NuRD (Nucleosome Remodeling and Deacetylation) complex is a repressive complex in gene transcription by modulating chromatin accessibility of target genes to transcription factors and RNA polymerase II. Although individual subunits of the complex have been implicated in many other cancer types, the complex's role in human hepatocellular carcinoma (HCC) is not fully understood. More importantly, the NuRD complex has not yet been investigated as a whole in cancers.

METHODS

We analyzed the expression of the NuRD complex in HCC and evaluated the prognostic value of NuRD complex expression in HCC using the RNA-seq data obtained from the TCGA project. We examined the effect of CHD4 knockdown on HCC cell proliferation, apoptosis, migration, invasion, epithelial-mesenchymal transition, colony-forming ability, and on complement gene expression. We also performed bioinformatic analyses to investigate the correlation between the NuRD complex expression and immune infiltration.

RESULTS

We found that nine subunits, out of 14 subunits of the NuRD complex examined, were significantly overexpressed in HCC, and their expression levels were positively correlated with cancer progression. More importantly, our data also demonstrated that these subunits tended to be overexpressed as a whole in HCC. Subsequent studies demonstrated that knockdown of CHD4 in HCC cells inhibits cell proliferation, migration, invasion, and colony-forming ability and promotes apoptosis of HCC cells, indicating that the CHD4/NuRD complex plays oncogenic roles in HCC. Further analysis revealed that the CHD4/NuRD complex regulates complement gene expression in HCC. Intriguingly, we found that the CHD4/NuRD complex expression was inversely correlated with CD8 T cell infiltration in HCC.

CONCLUSIONS

Our data demonstrate that the CHD4/NuRD complex plays an oncogenic role in human HCC and regulates complement gene expression in HCC cells. The results of inverse correlation between the CHD4/NuRD complex and CD8 T cell and DC cell infiltration in HCC suggest that the CHD4/NuRD complex not only plays direct regulatory roles in HCC cells, but also has an impact on the immune microenvironment of HCC.

摘要

背景

NuRD(核小体重塑和去乙酰化)复合物是一种转录抑制复合物,通过调节靶基因对转录因子和 RNA 聚合酶 II 的染色质可及性来调节基因转录。尽管该复合物的各个亚基已被牵连到许多其他癌症类型中,但该复合物在人类肝细胞癌(HCC)中的作用尚不完全清楚。更重要的是,整个 NuRD 复合物尚未在癌症中进行研究。

方法

我们分析了 HCC 中 NuRD 复合物的表达,并使用从 TCGA 项目获得的 RNA-seq 数据评估了 NuRD 复合物表达在 HCC 中的预后价值。我们检查了 CHD4 敲低对 HCC 细胞增殖、凋亡、迁移、侵袭、上皮-间充质转化、集落形成能力以及补体基因表达的影响。我们还进行了生物信息学分析,以研究 NuRD 复合物表达与免疫浸润之间的相关性。

结果

我们发现,在 HCC 中,14 个 NuRD 复合物亚基中有 9 个亚基显著过表达,其表达水平与癌症进展呈正相关。更重要的是,我们的数据还表明,这些亚基在 HCC 中往往整体过表达。随后的研究表明,在 HCC 细胞中敲低 CHD4 可抑制细胞增殖、迁移、侵袭和集落形成能力,并促进 HCC 细胞凋亡,表明 CHD4/NuRD 复合物在 HCC 中发挥致癌作用。进一步分析表明,CHD4/NuRD 复合物调节 HCC 中补体基因的表达。有趣的是,我们发现 CHD4/NuRD 复合物的表达与 HCC 中 CD8 T 细胞浸润呈负相关。

结论

我们的数据表明,CHD4/NuRD 复合物在人类 HCC 中发挥致癌作用,并调节 HCC 细胞中补体基因的表达。CHD4/NuRD 复合物与 HCC 中 CD8 T 细胞和 DC 细胞浸润呈负相关的结果表明,CHD4/NuRD 复合物不仅在 HCC 细胞中发挥直接调节作用,而且对 HCC 的免疫微环境也有影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3e2/7027061/5a3cc129097a/13148_2020_827_Fig1_HTML.jpg

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