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Jahangiri-Tazehkand, S.

Publications and source records attributed to Jahangiri-Tazehkand, S..

3 recordsLinked to original sources

Drug Sensitivity Prediction From Cell Line-Based Pharmacogenomics Data: Guidelines for Developing Machine Learning Models

The goal of precision oncology is to tailor treatment for patients individually using the genomic profile of their tumors. Pharmacogenomics datasets such as cancer cell lines are among the most valuable resources for drug sensitivity prediction, a crucial task of precision oncology. Machine learning methods have been employed to predict drug sensitivity based on the multiple omics data available for large panels of cancer cell lines. However, there are no comprehensive guidelines on how to properly train and validate such machine learning models for drug sensitivity prediction. In this paper, we introduce a set of guidelines for different aspects of training gene expression-based predictors using cell line datasets. These guidelines provide extensive analysis of the generalization of drug sensitivity predictors, and challenge many current practices in the community including the choice of training dataset and measure of drug sensitivity. Application of these guidelines in future studies will enable the development of more robust preclinical biomarkers.

bioinformatics↗

The Expression Pattern of miR-17, -24, -124 and -145 as Diagnostic Factor for Metastatic Gastric Cancer; a Lesson from Gastric Cancer Stem cells

BackgroundDistant metastasis of Gastric Cancer (GC) causes more than 700 000 deaths worldwide. Cancer Stem Cells (CSCs) are a subpopulation of cancer cells responsible for aggressiveness and chemoresistance in clinical settings. MicroRNAs (miRNAs) emerge as important players in regulating self-renewal and metastasis in CSCs. Understanding the role of miRNAs in CSCs offer a potential diagnostic tool for GC patients. This study is aimed to identify miRNAs that target both stemness and metastasis in gastric cancer stem cells (GCSCs) and differentially expressed in metastatic GC patients as diagnostic biomarkers for GC metastasis. MethodsWe investigate the gene expression profile of patients using the GEO database and Rstudio software. To obtain the regulatory networks and miRNAs, the STRING and miRwalk database used. The gastric cancer tissues were obtained from Iranian National Tumor Bank (INTB) to validate the results. ResultsOur results indicated three important regulatory cores affecting the immune systems regulation, tumor progress, and metastasis. Based on the bioinformatics results, four miRNAs miR-17-5p, miR-24-3p, miR-124-3p, and miR-145-5p, were selected, and their expression pattern was evaluated in 10 patients metastatic tumors compared to 10 nonmetastatic tumors by real-time PCR. The expression level of mir-17, -24, and -124 was upregulated about 8, 10, 60 folds, respectively, and miR-145 was down-regulated 4.5 folds in metastatic tumors compared to nonmetastatic tumors. Conclusionthe high expression level of miR-17, -24, -124, and low level of miR-145 in GC patients samples could be a potential biomarker for the presence of GCSCs and the diagnosis of metastasis.

cancer biology↗

PSL-Recommender: Protein Subcellular Localization Prediction using Recommender System

Identifying a proteins subcellular location is of great interest for understanding its function and behavior within the cell. In the last decade, many computational approaches have been proposed as a surrogate for expensive and inefficient wet-lab methods that are used for protein subcellular localization. Yet, there is still much room for improving the prediction accuracy of these methods.\n\nPSL-Recommender (Protein subcellular location recommender) is a method that employs neighborhood regularized logistic matrix factorization to build a recommender system for protein subcellular localization. The effectiveness of PSL-Recommender method is benchmarked on one human and three animals datasets. The results indicate that the PSL-Recommender significantly outperforms state-of-the-art methods, improving the previous best method up to 31% in F1 - mean, up to 28% in ACC, and up to 47% in AVG. The source of datasets and codes are available at: https://github.com/RJamali/PSL-Recommender

bioinformatics↗