利用mirna与竞争内源性rna的扰动相关性预测癌症的远处转移部位。

IF 2.6 4区 生物学 Q2 BIOLOGY Computational Biology and Chemistry Pub Date : 2025-01-16 DOI:10.1016/j.compbiolchem.2025.108353
Myeonghoon Cho , Byungkyu Park , Kyungsook Han
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引用次数: 0

摘要

癌症转移是指肿瘤细胞通过淋巴系统或血液从原发肿瘤部位扩散到身体的其他部位。转移是癌症相关死亡的主要原因。尽管在过去的几十年里,癌症研究和治疗取得了重大进展,但转移并没有被完全了解,也很难提前预测。特别是,远端转移比淋巴结转移更难预测,淋巴结转移是癌细胞向附近淋巴结的扩散。远端转移位点甚至比远端转移的发生更难预测,因为预测远端转移位点的问题是一个多类别和多标签的分类问题;远处转移部位(骨、肝、肺和其他器官)有两种以上的分类,单个样本可以有多个转移部位的多个标签。本文提出了一种基于个体癌症患者中miRNAs与竞争内源性rna (ceRNAs)的相关性变化预测远处转移部位的新方法。在多个癌症类型的独立数据集上进行的测试表明,该方法具有较高的预测性能。将我们的方法与其他最先进的方法进行比较,我们的方法表现出比其他方法更好和更稳定的性能。我们的方法可以作为确定治疗方案的有用辅助工具,通过预测早期癌症患者是否会发生转移以及在哪里发生转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Predicting distant metastatic sites of cancer using perturbed correlations of miRNAs with competing endogenous RNAs
Cancer metastasis is the dissemination of tumor cells from the primary tumor site to other parts of the body via the lymph system or bloodstream. Metastasis is the leading cause of cancer associated death. Despite the significant advances in cancer research and treatment over the past decades, metastasis is not fully understood and difficult to predict in advance. In particular, distant metastasis is more difficult to predict than lymph node metastasis, which is the spread of cancer cells to nearby lymph nodes. Distant metastatic sites is even more difficult to predict than the occurrence of distant metastasis because the problem of predicting distant metastatic sites is a multi-class and multi-label classification problem; there are more than two classes for distant metastatic sites (bone, liver, lung, and other organs), and a single sample can have multiple labels for multiple metastatic sites. This paper presents a new method for predicting distant metastatic sites based on correlation changes of miRNAs with competing endogenous RNAs (ceRNAs) in individual cancer patients. Testing the method on independent datasets of several cancer types demonstrated a high prediction performance. In comparison of our method with other state of the art methods, our method showed a much better and more stable performance than the others. Our method can be used as useful aids in determining treatment options by predicting if and where metastasis will occur in cancer patients at early stages.
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来源期刊
Computational Biology and Chemistry
Computational Biology and Chemistry 生物-计算机:跨学科应用
CiteScore
6.10
自引率
3.20%
发文量
142
审稿时长
24 days
期刊介绍: Computational Biology and Chemistry publishes original research papers and review articles in all areas of computational life sciences. High quality research contributions with a major computational component in the areas of nucleic acid and protein sequence research, molecular evolution, molecular genetics (functional genomics and proteomics), theory and practice of either biology-specific or chemical-biology-specific modeling, and structural biology of nucleic acids and proteins are particularly welcome. Exceptionally high quality research work in bioinformatics, systems biology, ecology, computational pharmacology, metabolism, biomedical engineering, epidemiology, and statistical genetics will also be considered. Given their inherent uncertainty, protein modeling and molecular docking studies should be thoroughly validated. In the absence of experimental results for validation, the use of molecular dynamics simulations along with detailed free energy calculations, for example, should be used as complementary techniques to support the major conclusions. Submissions of premature modeling exercises without additional biological insights will not be considered. Review articles will generally be commissioned by the editors and should not be submitted to the journal without explicit invitation. However prospective authors are welcome to send a brief (one to three pages) synopsis, which will be evaluated by the editors.
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