上皮-间质转化通路的调控及基于人工智能的通路活性预测模型

Onco Pub Date : 2023-01-06 DOI:10.3390/onco3010002
Shihori Tanabe, Sabina Quader, Ryuichi Ono, Horacio Cabral, Kazuhiko Aoyagi, Akihiko Hirose, Edward J. Perkins, Hiroshi Yokozaki, Hiroki Sasaki
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引用次数: 2

摘要

由于上皮-间充质转化(epithelial-mesenchymal transition, EMT)的活性参与抗癌耐药、癌症恶性,并且与癌症干细胞(cancer stem cells, CSCs)有一些共同的特征,我们使用人工智能(AI)建模来识别基因表达数据集中EMT相关通路的癌症相关活性。我们使用独创性途径分析(Ingenuity Pathway Analysis, IPA)生成了覆盖在分子途径上的基因表达图像。然后通过datarrobot自动化机器学习平台对发育路径中50个激活和50个未激活的EMT调控通路图像进行建模。最准确的模型是基于Elastic-Net Classifier算法。用另外10张激活和失活的通路图像对模型进行验证。生成的模型有假阳性和假阴性结果。这些图像具有明显的反标签特征,原始数据与帕金森病有关。这种方法可靠地确定了癌症表型和治疗方法,其中EMT调节在发育途径中被激活或灭活,从而确定了可能应用或开发治疗方法的条件。由于有各种各样的癌症表型和CSC靶点,为CSC耐药和癌症转移的机制提供了新的见解,我们的方法有望建模和模拟细胞表型转变,以及预测分子诱导的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulation of Epithelial–Mesenchymal Transition Pathway and Artificial Intelligence-Based Modeling for Pathway Activity Prediction
Because activity of the epithelial–mesenchymal transition (EMT) is involved in anti-cancer drug resistance, cancer malignancy, and shares some characteristics with cancer stem cells (CSCs), we used artificial intelligence (AI) modeling to identify the cancer-related activity of the EMT-related pathway in datasets of gene expression. We generated images of gene expression overlayed onto molecular pathways with Ingenuity Pathway Analysis (IPA). A dataset of 50 activated and 50 inactivated pathway images of EMT regulation in the development pathway was then modeled by the DataRobot Automated Machine Learning platform. The most accurate models were based on the Elastic-Net Classifier algorithm. The model was validated with 10 additional activated and 10 additional inactivated pathway images. The generated models had false-positive and false-negative results. These images had significant features of opposite labels, and the original data were related to Parkinson’s disease. This approach reliably identified cancer phenotypes and treatments where EMT regulation in the development pathway was activated or inactivated thereby identifying conditions where therapeutics might be applied or developed. As there are a wide variety of cancer phenotypes and CSC targets that provide novel insights into the mechanism of CSCs’ drug resistance and cancer metastasis, our approach holds promise for modeling and simulating cellular phenotype transition, as well as predicting molecular-induced responses.
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