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系统分析确定了由 RNA 结合蛋白 CELF1 控制的富含黑色素瘤的促癌基因网络。

Systems analysis identifies melanoma-enriched pro-oncogenic networks controlled by the RNA binding protein CELF1.

机构信息

Melanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Center (CNIO), 28029, Madrid, Spain.

Bioinformatics Unit, CNIO, 28029, Madrid, Spain.

出版信息

Nat Commun. 2017 Dec 21;8(1):2249. doi: 10.1038/s41467-017-02353-y.

DOI:10.1038/s41467-017-02353-y
PMID:29269732
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5740069/
Abstract

Melanomas are well-known for their altered mRNA expression profiles. Yet, the specific contribution of mRNA binding proteins (mRBPs) to melanoma development remains unclear. Here we identify a cluster of melanoma-enriched genes under the control of CUGBP Elav-like family member 1 (CELF1). CELF1 was discovered with a distinct prognostic value in melanoma after mining the genomic landscape of the 692 known mRBPs across different cancer types. Genome-wide transcriptomic, proteomic, and RNA-immunoprecipitation studies, together with loss-of-function analyses in cell lines, and histopathological evaluation in clinical biopsies, revealed an intricate repertoire of CELF1-RNA interactors with minimal overlap with other malignancies. This systems approach uncovered the oncogene DEK as an unexpected target and downstream effector of CELF1. Importantly, CELF1 and DEK were found to represent early-induced melanoma genes and adverse indicators of overall patient survival. These results underscore novel roles of CELF1 in melanoma, illustrating tumor type-restricted functions of RBPs in cancer.

摘要

黑色素瘤以其改变的 mRNA 表达谱而闻名。然而,mRNA 结合蛋白(mRBPs)对黑色素瘤发展的具体贡献仍不清楚。在这里,我们确定了一组受 CUGBP Elav 样家族成员 1(CELF1)调控的富含黑色素瘤的基因。在挖掘不同癌症类型中 692 种已知 mRBPs 的基因组景观后,CELF1 被发现具有独特的预后价值。全基因组转录组、蛋白质组和 RNA-免疫沉淀研究,以及细胞系中的功能丧失分析,以及临床活检中的组织病理学评估,揭示了 CELF1-RNA 相互作用体的复杂组合,与其他恶性肿瘤的重叠最小。这种系统方法揭示了 DEK 作为 CELF1 的意外靶标和下游效应子的致癌基因。重要的是,发现 CELF1 和 DEK 分别代表早期诱导的黑色素瘤基因和患者总生存的不利指标。这些结果强调了 CELF1 在黑色素瘤中的新作用,说明了 RBP 在癌症中的肿瘤类型特异性功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8583/5740069/417fe9768d8c/41467_2017_2353_Fig7_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8583/5740069/b7040460e2d7/41467_2017_2353_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8583/5740069/417fe9768d8c/41467_2017_2353_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8583/5740069/353d45c6afaa/41467_2017_2353_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8583/5740069/10274f4f953d/41467_2017_2353_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8583/5740069/5e9dbf798e3c/41467_2017_2353_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8583/5740069/c1d35c47f3bf/41467_2017_2353_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8583/5740069/94741097865e/41467_2017_2353_Fig5_HTML.jpg
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