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Identifying Genes Associated with the Anticancer Activity of a Fluorinated Chalcone in Triple-Negative Breast Cancer
Eduardo De la Cruz-Cano1, José Ángel González-Díaz1, Ivonne María Olivares-Corichi2
1Laboratorio de Bioquímica y Biología Molecular, División Académica de Ciencias Básicas, Centro de Investigación de Ciencia y Tecnología Aplicada de Tabasco (CICTAT), Universidad Juárez Autónoma de Tabasco, Cunduacán C.P. 86690, Mexico.
Abstract:
Fluorinated chalcones are molecules reported to possess potent anticancer properties against triple-negative breast cancer (TNBC) cells. However, their molecular mechanisms have not yet been fully explored. Using bioinformatics tools, we analyzed the transcriptomes of MDA-MB-231 cells treated with either a novel fluorinated chalcone (compound 3) or a control in order to identify differentially expressed (DE) genes associated with its anticancer activity and determine the biological processes in which these genes are involved. A fluorinated chalcone was synthesized using the Claisen-Schmidt method. The transcriptome of MDA-MB-231 cells was then analyzed on an Illumina NextSeq500, and DE genes with significant changes in expression were identified using the DESeq2 v1.38.0 bioinformatics tool under the strict detection criteria of |log2FC| ≥ 2 and adjusted p < 0.05. We identified 504 DE genes, which were enriched in terms related to "regulation of cell death", "cation transport", "response to topologically incorrect proteins", and "response to unfolded proteins". Surprisingly, these genes were involved in "the HSF1-dependent transactivation pathway" and "the attenuation phase pathway". This bioinformatics-based study suggests that the tested fluorinated chalcone could influence HSF-1 silencing in addition to promoting the up-regulation of several genes involved in stress-induced apoptosis. Therefore, the tested compound could have enormous potential as a novel approach for TNBC treatment.
Insights
Novel fluorinated chalcones show promise for triple-negative breast cancer (TNBC) treatment. This study identified key genes and pathways, including HSF1 regulation and stress-induced apoptosis, offering new therapeutic strategies for TNBC.
Area of Science:
- Molecular Biology
- Bioinformatics
- Oncology
Background:
- Fluorinated chalcones exhibit anticancer properties against triple-negative breast cancer (TNBC).
- The precise molecular mechanisms underlying their efficacy remain underexplored.
Purpose of the Study:
- To investigate the molecular mechanisms of a novel fluorinated chalcone (compound 3) against TNBC cells.
- To identify differentially expressed genes and associated biological pathways affected by compound 3 treatment.
Main Methods:
- Synthesis of a novel fluorinated chalcone via Claisen-Schmidt reaction.
- Transcriptome analysis of MDA-MB-231 cells using Illumina NextSeq500.
- Bioinformatic identification of differentially expressed genes (|log2FC| ≥ 2, adjusted p < 0.05) using DESeq2.
Main Results:
- Identified 504 differentially expressed genes in response to compound 3.
- Enrichment analysis revealed involvement in "regulation of cell death" and "response to unfolded proteins".
- Discovered involvement in "HSF1-dependent transactivation pathway" and "attenuation phase pathway".
Conclusions:
- The fluorinated chalcone may modulate HSF1 silencing.
- Compound 3 up-regulates genes involved in stress-induced apoptosis.
- This compound holds potential as a novel therapeutic agent for TNBC.
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