AMLdb:鉴定急性髓性白血病生物标志物和药物靶点的综合性多组学平台。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Keerthana Vinod Kumar, Ambuj Kumar, Kavita Kundal, Avik Sengupta, Kunjulakshmi R, Subashani Singh, Bhanu Teja Korra, Simran Sharma, Vandana Suresh, Mayilaadumveettil Nishana, Rahul Kumar
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引用次数: 0

摘要

急性髓性白血病(AML)是成人主要的白血病恶性肿瘤之一。这种疾病的异质性给诊断和治疗带来了极大的困难。随着下一代测序(NGS)技术的出现,在分子水平上探索生物标志物和药物靶点已成为研究人员的工作重点,以便提出新的疗法,改善急性髓细胞白血病患者的预后和生存状况。然而,来自 NGS 平台的海量数据需要一个全面的 AML 平台来简化文献挖掘工作并节省时间。为此,我们开发了一个交互式多组学平台 AMLdb,允许用户查询、可视化、检索和分析 AML 相关的多组学数据。AMLdb 包含 86 个基因表达谱数据集、15 个甲基化谱数据集、26 个 AML 细胞系的 CRISPR-Cas9 基因敲除筛选、26 个 AML 细胞系对 288 种药物的敏感性、23 个 AML 细胞系中 41 个独特基因的突变以及 41 个实验验证生物标志物的信息。在本研究中,我们报告了通过 AMLdb 分析发现的五个基因,即 CBFB、ENO1、IMPDH2、SEPHS2 和 MYH9。ENO1是唯一被发现的基因,作为一个新的潜在靶点还需要进一步研究,而其他报告的基因之前已通过实验研究证实为靶点。最重要的是,我们相信利用 AMLdb 的这些发现可以使其成为加快开发急性髓细胞性白血病有效疗法的宝贵资源,并帮助研究界加深对急性髓细胞性白血病发病机制的了解。AMLdb 可在 https://project.iith.ac.in/cgntlab/amldb 免费获取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
AMLdb: a comprehensive multi-omics platform to identify biomarkers and drug targets for acute myeloid leukemia.

Acute myeloid leukemia (AML) is one of the leading leukemic malignancies in adults. The heterogeneity of the disease makes the diagnosis and treatment extremely difficult. With the advent of next-generation sequencing (NGS) technologies, exploration at the molecular level for the identification of biomarkers and drug targets has been the focus for the researchers to come up with novel therapies for better prognosis and survival outcomes of AML patients. However, the huge amount of data from NGS platforms requires a comprehensive AML platform to streamline literature mining efforts and save time. To facilitate this, we developed AMLdb, an interactive multi-omics platform that allows users to query, visualize, retrieve, and analyse AML related multi-omics data. AMLdb contains 86 datasets for gene expression profiles, 15 datasets for methylation profiles, CRISPR-Cas9 knockout screens of 26 AML cell lines, sensitivity of 26 AML cell lines to 288 drugs, mutations in 41 unique genes in 23 AML cell lines, and information on 41 experimentally validated biomarkers. In this study, we have reported five genes, i.e. CBFB, ENO1, IMPDH2, SEPHS2, and MYH9 identified via our analysis using AMLdb. ENO1 is uniquely identified gene which requires further investigation as a novel potential target while other reported genes have been previously confirmed as targets through experimental studies. Top of form we believe that these findings utilizing AMLdb can make it an invaluable resource to accelerate the development of effective therapies for AML and assisting the research community in advancing their understanding of AML pathogenesis. AMLdb is freely available at https://project.iith.ac.in/cgntlab/amldb.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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