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Published on: April 22, 2021
Molecular-level effects of eribulin and paclitaxel on breast cancer based on differential co-expression network
Abstract:
We investigated the effects of eribulin and paclitaxel on breast cancer (BC) by exploring molecular biomarkers and pathways. Co-expression networks were constructed by differentially co-expressed genes and links, and centralities were analyzed to explore the hub genes. Pathway-enrichment analysis was performed. The hub genes were validated using the polymerase chain reaction and western blotting. A total of 132 and 153 differentially expressed genes were identified in BC cell lines treated with eribulin and paclitaxel, respectively. Six hub genes were identified in two co-expression networks. The spliceosome pathway was the mutually significant pathway. The validation analysis was basically consistent with the bioinformatics. We successfully identified several hub genes and pathways relevant to the effects of eribulin and paclitaxel on BC based on the network analysis.
Insights
Eribulin and paclitaxel impact breast cancer (BC) by altering gene expression. Network analysis identified key genes and the spliceosome pathway involved in their effects on BC.
Area of Science:
- Oncology
- Genomics
- Bioinformatics
Background:
- Breast cancer (BC) treatment involves chemotherapeutic agents like eribulin and paclitaxel.
- Understanding the molecular mechanisms of these drugs is crucial for optimizing BC therapy.
Purpose of the Study:
- To investigate the molecular biomarkers and pathways affected by eribulin and paclitaxel in breast cancer.
- To identify potential therapeutic targets through network analysis.
Main Methods:
- Differential gene expression analysis was performed on BC cell lines treated with eribulin and paclitaxel.
- Co-expression network construction and hub gene identification using network centrality.
- Pathway-enrichment analysis to identify significantly affected biological pathways.
- Validation of identified hub genes using polymerase chain reaction and western blotting.
Main Results:
- 132 differentially expressed genes were identified with eribulin treatment and 153 with paclitaxel treatment.
- Six hub genes were identified across two co-expression networks.
- The spliceosome pathway was identified as a significantly enriched pathway common to both treatments.
- Bioinformatic findings were largely consistent with experimental validation.
Conclusions:
- Eribulin and paclitaxel exert their effects on breast cancer through distinct and overlapping molecular mechanisms.
- Network analysis successfully identified key genes and pathways, including the spliceosome, relevant to eribulin and paclitaxel action in BC.
- The identified hub genes and pathways may represent potential targets for future breast cancer therapies.

