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DSPLMF:一种在逻辑矩阵分解中使用新型正则化方法进行癌症药物敏感性预测的方法。

DSPLMF: A Method for Cancer Drug Sensitivity Prediction Using a Novel Regularization Approach in Logistic Matrix Factorization.

作者信息

Emdadi Akram, Eslahchi Changiz

机构信息

Department of Computer Sciences, Faculty of Mathematics, Shahid Beheshti University, Tehran, Iran.

School of Biological Sciences, Institute for Research in Fundamental Sciences (IPM), Tehran, Iran.

出版信息

Front Genet. 2020 Feb 27;11:75. doi: 10.3389/fgene.2020.00075. eCollection 2020.

DOI:10.3389/fgene.2020.00075
PMID:32174963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7056895/
Abstract

The ability to predict the drug response for cancer disease based on genomics information is an essential problem in modern oncology, leading to personalized treatment. By predicting accurate anticancer responses, oncologists achieve a complete understanding of the effective treatment for each patient. In this paper, we present DSPLMF (rug ensitivity rediction using ogistic atrix actorization) approach based on Recommender Systems. DSPLMF focuses on discovering effective features of cell lines and drugs for computing the probability of the cell lines are sensitive to drugs by logistic matrix factorization approach. Since similar cell lines and similar drugs may have similar drug responses and incorporating similarities between cell lines and drugs can potentially improve the drug response prediction, gene expression profile, copy number alteration, and single-nucleotide mutation information are used for cell line similarity and chemical structures of drugs are used for drug similarity. Evaluation of the proposed method on CCLE and GDSC datasets and comparison with some of the state-of-the-art methods indicates that the result of DSPLMF is significantly more accurate and more efficient than these methods. To demonstrate the ability of the proposed method, the obtained latent vectors are used to identify subtypes of cancer of the cell line and the predicted IC50 values are used to depict drug-pathway associations. The source code of DSPLMF method is available in https://github.com/emdadi/DSPLMF.

摘要

基于基因组学信息预测癌症疾病药物反应的能力是现代肿瘤学中的一个关键问题,这有助于实现个性化治疗。通过准确预测抗癌反应,肿瘤学家能够全面了解针对每位患者的有效治疗方法。在本文中,我们提出了基于推荐系统的DSPLMF(使用逻辑矩阵分解预测药物敏感性)方法。DSPLMF专注于通过逻辑矩阵分解方法发现细胞系和药物的有效特征,以计算细胞系对药物敏感的概率。由于相似的细胞系和相似的药物可能具有相似的药物反应,纳入细胞系和药物之间的相似性可能会提高药物反应预测的准确性,因此基因表达谱、拷贝数改变和单核苷酸突变信息用于细胞系相似性分析,药物的化学结构用于药物相似性分析。在CCLE和GDSC数据集上对所提出方法进行评估,并与一些现有最先进的方法进行比较,结果表明DSPLMF的结果比这些方法显著更准确、更高效。为了证明所提出方法的能力,所获得的潜在向量用于识别细胞系癌症的亚型,预测的IC50值用于描述药物-通路关联。DSPLMF方法的源代码可在https://github.com/emdadi/DSPLMF获取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d384/7056895/1d72cd5d2211/fgene-11-00075-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d384/7056895/9063dac5edfc/fgene-11-00075-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d384/7056895/f94b33916172/fgene-11-00075-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d384/7056895/b9fc20ac7b4e/fgene-11-00075-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d384/7056895/6913bc5131d4/fgene-11-00075-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d384/7056895/306f2a312c77/fgene-11-00075-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d384/7056895/1d72cd5d2211/fgene-11-00075-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d384/7056895/9063dac5edfc/fgene-11-00075-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d384/7056895/f94b33916172/fgene-11-00075-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d384/7056895/b9fc20ac7b4e/fgene-11-00075-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d384/7056895/6913bc5131d4/fgene-11-00075-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d384/7056895/306f2a312c77/fgene-11-00075-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d384/7056895/1d72cd5d2211/fgene-11-00075-g006.jpg

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Anti-cancer Drug Response Prediction Using Neighbor-Based Collaborative Filtering with Global Effect Removal.使用基于邻居的协同过滤并去除全局效应进行抗癌药物反应预测。
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Predicting Cancer Drug Response using a Recommender System.
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