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Editor’s introduction to this issue (GI 19:1 2021)

机译:编辑对此问题的介绍(G&I 19:12021)

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摘要

In this issue, there are 10 Original Articles, of which five are related to cancer research. The first original article, by the group of Han et al. (Ewha Womans University, Korea), focused on elucidating the molecular mechanisms of acquired resistance to BRAF inhibitors in melanoma. A microfluidic chip with a concentration gradient of vemurafenib was utilized to rapidly obtain therapy-resistant clones from two melanoma cell lines with the BRAFV600E mutation. Exome and transcriptome data were produced from 13 resistant clones. This study provides an omics-based comprehensive overview of the molecular mechanisms governing acquired resistance to BRAF inhibitor therapy. The second article, by Lee and Jung (KAIST, Korea), reported functional annotation of lung cancer-associated genetic variants based on eight major cell types of human lung tissue. This work showed that approximately 22% of lung cancer-associated risk variants were linked to noncoding regulatory elements. Through integrative analysis of high-resolution long-range chromatin interactome maps and single-cell RNA-sequencing data, the authors uncovered a number of putative target genes of these variants and functionally relevant cell types, which expands the scope of functional annotation of lung cancer-associated genetic risk factors.
机译:在这个问题中,有10篇原始文章,其中五篇文章与癌症研究有关。第一个原始文章,由汉等人群。 (Ewha Womans University,韩国),专注于阐明黑色素瘤中获得性耐药性的抗性的分子机制。利用具有vemuRafenib的浓度梯度的微流体芯片从2个黑色素瘤细胞系中快速获得抗治疗耐药克隆,并用BRAFV600E突变。 Exome和转录组数据由13个抗克隆产生。本研究提供了基于OMICS的综合性概述了治疗对BRAF抑制剂治疗的抗性的分子机制。基于八种人肺组织的八种主要细胞类型,李和钟(Kaist,Kaist,Kaist)的第二篇文章报道了肺癌相关遗传变异的功能注释。这项工作表明,大约22%的肺癌相关的风险变体与非编码调节元件有关。通过对高分辨率远程染色质蛋白质地图和单细胞RNA测序数据的综合分析,作者发现了这些变体的许多推定的靶基因和功能相关的细胞类型,这扩大了肺癌功能性注释的范围 - 分配的遗传危险因素。

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