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TCGA 泛癌症转录组数据中鉴定的癌症相关 KRAB-ZNF 因子的表达特征。

The expression signature of cancer-associated KRAB-ZNF factors identified in TCGA pan-cancer transcriptomic data.

机构信息

Department of Cancer Immunology, Poznan University of Medical Sciences, Poland.

Department of Diagnostics and Cancer Immunology, Greater Poland Cancer Centre, Poznan, Poland.

出版信息

Mol Oncol. 2019 Apr;13(4):701-724. doi: 10.1002/1878-0261.12407. Epub 2019 Feb 16.

DOI:10.1002/1878-0261.12407
PMID:30444046
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6442004/
Abstract

The KRAB-ZNF (Krüppel-associated box domain zinc finger) gene family is composed of a large number of highly homologous genes, gene isoforms, and pseudogenes. The proteins encoded by these genes, whose expression is often tissue-specific, act as epigenetic suppressors contributing to the addition of repressive chromatin marks and DNA methylation. Due to its high complexity, the KRAB-ZNF family has not been studied in sufficient detail, and the involvement of its members in carcinogenesis remains mostly unexplored. In this study, we aimed to provide a comprehensive description of cancer-associated KRAB-ZNFs using publicly available The Cancer Genome Atlas pan-cancer datasets. We analyzed 6727 tumor and normal tissue samples from 16 cancer types. Here, we showed that a small but distinctive cluster of 16 KRAB-ZNFs is commonly upregulated across multiple cancer cohorts in comparison to normal samples. We confirmed these observations in the independent panels of lung and breast cancer cell lines and tissues. This upregulation was also observed for most of the KRAB-ZNF splicing variants, whose expression is simultaneously upregulated in tumors compared to normal tissues. Finally, by analyzing the clinicopathological data for breast and lung cancers, we demonstrated that the expression of cancer-associated KRAB-ZNFs correlates with patient survival, tumor histology, and molecular subtyping. Altogether, our study allowed the identification and characterization of KRAB-ZNF factors that may have an essential function in cancer biology and thus potential to become novel oncologic biomarkers and treatment targets.

摘要

Krüppel 相关盒结构域锌指(KRAB-ZNF)基因家族由大量高度同源的基因、基因异构体和假基因组成。这些基因编码的蛋白质表达通常具有组织特异性,作为表观遗传抑制剂发挥作用,有助于添加抑制性染色质标记和 DNA 甲基化。由于其高度复杂性,KRAB-ZNF 家族尚未得到充分研究,其成员在致癌作用中的参与仍在很大程度上未被探索。在这项研究中,我们旨在使用公共可用的癌症基因组图谱泛癌症数据集,全面描述与癌症相关的 KRAB-ZNF。我们分析了来自 16 种癌症类型的 6727 个肿瘤和正常组织样本。在这里,我们表明,与正常样本相比,在多个癌症队列中,一小部分但独特的 16 个 KRAB-ZNF 通常会上调。我们在独立的肺癌和乳腺癌细胞系和组织面板中证实了这些观察结果。这种上调也发生在大多数 KRAB-ZNF 剪接变体中,与正常组织相比,其在肿瘤中的表达同时上调。最后,通过分析乳腺癌和肺癌的临床病理数据,我们证明了与癌症相关的 KRAB-ZNF 的表达与患者生存、肿瘤组织学和分子亚型相关。总的来说,我们的研究鉴定和描述了 KRAB-ZNF 因子,它们可能在癌症生物学中具有重要功能,因此有可能成为新的肿瘤标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/6989d7353c4c/MOL2-13-701-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/d61323eb27ce/MOL2-13-701-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/283bb9f8bedb/MOL2-13-701-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/0326c2eb8bcf/MOL2-13-701-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/8846b1b2ab5a/MOL2-13-701-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/120b8d1e1107/MOL2-13-701-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/6989d7353c4c/MOL2-13-701-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/d61323eb27ce/MOL2-13-701-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/8039af6f903c/MOL2-13-701-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/b32a128d3e4f/MOL2-13-701-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/ff722f194434/MOL2-13-701-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/283bb9f8bedb/MOL2-13-701-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/0326c2eb8bcf/MOL2-13-701-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/8846b1b2ab5a/MOL2-13-701-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/120b8d1e1107/MOL2-13-701-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95da/6442004/6989d7353c4c/MOL2-13-701-g009.jpg

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