利用人工智能诊断乳腺癌的突变特征。

IF 2.1 Q3 ONCOLOGY
Patrick Odhiambo, Harrison Okello, Annette Wakaanya, Clabe Wekesa, Patrick Okoth
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引用次数: 0

摘要

背景:乳腺癌是世界范围内最常见的女性癌症。它的诊断和预后仍然很少,不精确,文献记录也很差。先前的研究表明,一些基因突变特征被怀疑会导致各种乳腺癌的进展。关于人工智能工具在描述乳腺癌突变特征方面的作用的数据缺乏。本研究旨在利用人工智能模型研究乳腺癌基因突变谱之间的关系,以期基于乳腺癌基因特征建立准确的预后预测。先前对乳腺癌的研究是基于症状、起源和肿瘤大小。目前还没有研究是否可以利用Cytoscape、Phenolyzer和genshot等具有更好预后潜力的人工智能平台来诊断乳腺癌。这是有史以来首次尝试使用不同的人工智能平台进行乳腺癌诊断的组合方法。方法:人工智能(AI)是一种模拟人类认知能力的数学算法,可以解决复杂的医疗保健问题,如乳腺癌等复杂的生物异常。目前的模型旨在通过将成像表型与基因突变、肿瘤概况和激素受体状态以及结合肿瘤和患者特异性特征的成像生物标志物的发展相关联来预测结果和预后。Geneshotsav 2021、Cytoscape 3.9.1和Phenolyzer Nature Methods, 12:841-843(2015)工具被用于挖掘乳腺癌相关的突变特征,并为识别途径和丰富的相似基因网络提供有用的替代计算工具,其总体目标是提供导致乳腺癌发展的各种突变过程的系统视图。大量数据集的收集和诊断标记等工具的使用将有助于开发量身定制的新型药物,以及分发前瞻性治疗方案。结果:特定的dna维持缺陷、内源性或环境暴露和癌症基因组特征是相关的。在PubMed数据库(genshot)中搜索这些关键词,总共产生了21921个与乳腺癌相关的基因。然后,根据它们导致基因突变的倾向,使用Phenolyzer软件筛选这些基因。这些平台证实了这样一个事实,即使用Cytoscape 3.9.1、Phenolyzer和genesshot 2021进行乳腺癌诊断,揭示了以下突变特征:BRCA1、BRCA2、TP53、CHEK2、PTEN、CDH1、BRIP1、RAD51C、CASP3、CREBBP和SMAD3。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mutational signatures for breast cancer diagnosis using artificial intelligence.

Background: Breast cancer is the most common female cancer worldwide. Its diagnosis and prognosis remain scanty, imprecise, and poorly documented. Previous studies have indicated that some genetic mutational signatures are suspected to lead to progression of various breast cancer scenarios. There is paucity of data on the role of AI tools in delineating breast cancer mutational signatures. This study sought to investigate the relationship between breast cancer genetic mutational profiles using artificial intelligence models with a view to developing an accurate prognostic prediction based on breast cancer genetic signatures. Prior research on breast cancer has been based on symptoms, origin, and tumor size. It has not been investigated whether diagnosis of breast cancer can be made utilizing AI platforms like Cytoscape, Phenolyzer, and Geneshot with potential for better prognostic power. This is the first ever attempt for a combinatorial approach to breast cancer diagnosis using different AI platforms.

Method: Artificial intelligence (AI) are mathematical algorithms that simulate human cognitive abilities and solve difficult healthcare issues such as complicated biological abnormalities like those experienced in breast cancer scenarios. The current models aimed to predict outcomes and prognosis by correlating imaging phenotypes with genetic mutations, tumor profiles, and hormone receptor status and development of imaging biomarkers that combine tumor and patient-specific features. Geneshotsav 2021, Cytoscape 3.9.1, and Phenolyzer Nature Methods, 12:841-843 (2015) tools, were used to mine breast cancer-associated mutational signatures and provided useful alternative computational tools for discerning pathways and enriched networks of genes of similarity with the overall goal of providing a systematic view of the variety of mutational processes that lead to breast cancer development. The development of novel-tailored pharmaceuticals, as well as the distribution of prospective treatment alternatives, would be aided by the collection of massive datasets and the use of such tools as diagnostic markers.

Results: Specific DNA-maintenance defects, endogenous or environmental exposures, and cancer genomic signatures are connected. The PubMed database (Geneshot) search for the keywords yielded a total of 21,921 genes associated with breast cancer. Then, based on their propensity to result in gene mutations, the genes were screened using the Phenolyzer software. These platforms lend credence to the fact that breast cancer diagnosis using Cytoscape 3.9.1, Phenolyzer, and Geneshot 2021 reveals high profile of the following mutational signatures: BRCA1, BRCA2, TP53, CHEK2, PTEN, CDH1, BRIP1, RAD51C, CASP3, CREBBP, and SMAD3.

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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
46
审稿时长
11 weeks
期刊介绍: As the official publication of the National Cancer Institute, Cairo University, the Journal of the Egyptian National Cancer Institute (JENCI) is an open access peer-reviewed journal that publishes on the latest innovations in oncology and thereby, providing academics and clinicians a leading research platform. JENCI welcomes submissions pertaining to all fields of basic, applied and clinical cancer research. Main topics of interest include: local and systemic anticancer therapy (with specific interest on applied cancer research from developing countries); experimental oncology; early cancer detection; randomized trials (including negatives ones); and key emerging fields of personalized medicine, such as molecular pathology, bioinformatics, and biotechnologies.
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