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基因组分析显示蕈样肉芽肿中 JAK-STAT 信号通路抑制剂 HNRNPK 和 SOCS1 经常缺失。

Genomic analysis reveals recurrent deletion of JAK-STAT signaling inhibitors HNRNPK and SOCS1 in mycosis fungoides.

机构信息

Department of Dermatology, Leiden University Medical Center, Leiden, The Netherlands.

Sequencing Analysis Support Core, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

Genes Chromosomes Cancer. 2018 Dec;57(12):653-664. doi: 10.1002/gcc.22679. Epub 2018 Oct 25.

Abstract

Mycosis fungoides (MF) is the most common cutaneous T-cell lymphoma (CTCL). Causative genetic alterations in MF are unknown. The low recurrence of pathogenic small-scale mutations (ie, nucleotide substitutions, indels) in the disease, calls for the study of additional aspects of MF genetics. Here, we investigated structural genomic alterations in tumor-stage MF by integrating whole-genome sequencing and RNA-sequencing. Multiple genes with roles in cell physiology (n = 113) and metabolism (n = 92) were found to be impacted by genomic rearrangements, including 47 genes currently implicated in cancer. Fusion transcripts involving genes of interest such as DOT1L, KDM6A, LIFR, TP53, and TP63 were also observed. Additionally, we identified recurrent deletions of genes involved in cell cycle control, chromatin regulation, the JAK-STAT pathway, and the PI-3-K pathway. Remarkably, many of these deletions result from genomic rearrangements. Deletion of tumor suppressors HNRNPK and SOCS1 were the most frequent genetic alterations in MF after deletion of CDKN2A. Notably, SOCS1 deletion could be detected in early-stage MF. In agreement with the observed genomic alterations, transcriptome analysis revealed up-regulation of the cell cycle, JAK-STAT, PI-3-K and developmental pathways. Our results position inactivation of HNRNPK and SOCS1 as potential driver events in MF development.

摘要

蕈样肉芽肿(MF)是最常见的皮肤 T 细胞淋巴瘤(CTCL)。MF 的致病遗传改变尚不清楚。该疾病中致病性小范围突变(即核苷酸取代、缺失)的低复发率,需要研究 MF 遗传学的其他方面。在这里,我们通过整合全基因组测序和 RNA 测序研究了肿瘤期 MF 的结构基因组改变。发现包括 47 个目前与癌症相关的基因在内的多个参与细胞生理(n=113)和代谢(n=92)的基因受到基因组重排的影响。还观察到涉及感兴趣基因的融合转录本,如 DOT1L、KDM6A、LIFR、TP53 和 TP63。此外,我们还鉴定了参与细胞周期控制、染色质调节、JAK-STAT 途径和 PI-3-K 途径的基因的高频缺失。值得注意的是,这些缺失中的许多是由于基因组重排引起的。在 CDKN2A 缺失后,HNRNPK 和 SOCS1 肿瘤抑制基因的缺失是 MF 中最常见的遗传改变。值得注意的是,SOCS1 缺失可在早期 MF 中检测到。与观察到的基因组改变一致,转录组分析显示细胞周期、JAK-STAT、PI-3-K 和发育途径的上调。我们的研究结果将 HNRNPK 和 SOCS1 的失活定位为 MF 发展的潜在驱动事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b945/6282857/7b0543d3c815/GCC-57-653-g001.jpg

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