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通过外显子组测序鉴定犬口腔黏膜黑色素瘤中的突变,并与人类黑色素瘤进行比较。

Identification of mutations in canine oral mucosal melanomas by exome sequencing and comparison with human melanomas.

机构信息

Laboratory of Experimental and Comparative Oncology, Department of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, SP, Brazil.

Omixlab - Laboratory of Bioinformatics, Federal University of Pelotas, Pelotas, RS, Brazil.

出版信息

Sci Rep. 2024 Oct 15;14(1):24174. doi: 10.1038/s41598-024-74748-z.

Abstract

Oral mucosal melanomas (OMMs) are aggressive neoplasms commonly found in dogs but rare in humans. Utilizing whole exome sequencing (WES), which focuses on protein-coding regions to reveal mutation profiles, we conducted a comparative analysis of canine OMM and human melanomas. This study involved DNA extraction, exome enrichment, and sequencing from three canine OMM cell lines (CMGD-2, CMGD-5, TLM-1), five canine OMM frozen samples, a human OMM cell line (MEMO), and a human commercial skin melanoma cell line (SK-MEL-28). The sequencing and subsequent analysis of FASTQ files yielded final variant files, leading to the identification of mutations. Our findings revealed a total of 500 mutated genes in canine OMM, including significant ones such as EP300, FAT4, JAK3, LRP1B, NCOR1, and NOTCH1. Notably, 82 shared mutations were identified between human melanomas and canine OMM genomes. These mutations were categorized based on the gene functions. The identification of these mutations provides critical insights that can pave the way for the development of novel therapeutic strategies for both canine and human OMM, offering hope for more effective treatments in the future.

摘要

口腔黏膜黑色素瘤(OMM)是一种常见于犬类但罕见于人类的侵袭性肿瘤。本研究利用全外显子组测序(WES),专注于蛋白质编码区域以揭示突变谱,对犬类 OMM 和人类黑色素瘤进行了比较分析。该研究涉及从三个犬类 OMM 细胞系(CMGD-2、CMGD-5、TLM-1)、五个犬类 OMM 冷冻样本、一个人类 OMM 细胞系(MEMO)和一个人类商业皮肤黑色素瘤细胞系(SK-MEL-28)中提取 DNA、外显子富集和测序。对 FASTQ 文件的测序和后续分析产生了最终的变异文件,从而鉴定出突变。我们的研究结果在犬类 OMM 中共发现了 500 个突变基因,其中包括 EP300、FAT4、JAK3、LRP1B、NCOR1 和 NOTCH1 等重要基因。值得注意的是,在人类黑色素瘤和犬类 OMM 基因组之间发现了 82 个共享突变。这些突变是根据基因功能进行分类的。这些突变的鉴定为开发犬类和人类 OMM 的新型治疗策略提供了关键的见解,为未来更有效的治疗方法带来了希望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d751/11480479/439ea7e1c1a7/41598_2024_74748_Fig1_HTML.jpg

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