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Identification of Differentially Expressed Genes between Original Breast Cancer and Xenograft Using Machine Learning
Deling Wang1,2, Jia-Rui Li3, Yu-Hang Zhang4
1Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China. wangdl@sysucc.org.cn.
Abstract:
Breast cancer is one of the most common malignancies in women. Patient-derived tumor xenograft (PDX) model is a cutting-edge approach for drug research on breast cancer. However, PDX still exhibits differences from original human tumors, thereby challenging the molecular understanding of tumorigenesis. In particular, gene expression changes after tissues are transplanted from human to mouse model. In this study, we propose a novel computational method by incorporating several machine learning algorithms, including Monte Carlo feature selection (MCFS), random forest (RF), and rough set-based rule learning, to identify genes with significant expression differences between PDX and original human tumors. First, 831 breast tumors, including 657 PDX and 174 human tumors, were collected. Based on MCFS and RF, 32 genes were then identified to be informative for the prediction of PDX and human tumors and can be used to construct a prediction model. The prediction model exhibits a Matthews coefficient correlation value of 0.777. Seven interpretable interactions within the informative gene were detected based on the rough set-based rule learning. Furthermore, the seven interpretable interactions can be well supported by previous experimental studies. Our study not only presents a method for identifying informative genes with differential expression but also provides insights into the mechanism through which gene expression changes after being transplanted from human tumor into mouse model. This work would be helpful for research and drug development for breast cancer.
Insights
This study introduces a new computational method to find gene expression differences between patient-derived tumor xenograft (PDX) models and original human breast tumors. The findings aid in understanding gene expression changes and support breast cancer research and drug development.
Area of Science:
- Oncology
- Computational Biology
- Genomics
Background:
- Breast cancer is a prevalent malignancy in women.
- Patient-derived tumor xenograft (PDX) models are crucial for breast cancer drug research.
- Differences in gene expression between PDX models and original human tumors pose challenges for molecular understanding.
Purpose of the Study:
- To develop a novel computational method for identifying genes with significant expression differences between PDX and human breast tumors.
- To gain insights into the mechanisms of gene expression alteration during xenograft transplantation.
- To support breast cancer research and drug development.
Main Methods:
- Utilized a dataset of 831 breast tumors (657 PDX, 174 human).
- Employed machine learning algorithms: Monte Carlo feature selection (MCFS) and random forest (RF) to identify informative genes.
- Applied rough set-based rule learning to detect interpretable gene interactions.
Main Results:
- Identified 32 informative genes for distinguishing PDX from human tumors using MCFS and RF.
- Developed a prediction model with a Matthews coefficient correlation of 0.777.
- Discovered seven interpretable gene interactions supported by existing literature.
Conclusions:
- The proposed computational method effectively identifies informative genes with differential expression between PDX and human tumors.
- The findings provide valuable insights into gene expression changes post-xenotransplantation.
- This research contributes to advancing breast cancer studies and therapeutic development.
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