# Identifying Genes Associated with the Anticancer Activity of a Fluorinated Chalcone in Triple-Negative Breast Cancer Cells Using Bioinformatics Tools

**Authors:** Eduardo De la Cruz-Cano, José Ángel González-Díaz, Ivonne María Olivares-Corichi, Jorge Tonatiuh Ayala-Sumuano, José Alfredo Díaz-Gandarilla, Quirino Torres-Sauret, Violeta Larios-Serrato, Miguel Ángel Vilchis-Reyes, Carlos Javier López-Victorio, José Arnold González-Garrido, José Rubén García-Sánchez

PMC · DOI: 10.3390/ijms26083662 · 2025-04-12

## TL;DR

This study uses bioinformatics to identify genes affected by a fluorinated chalcone in triple-negative breast cancer cells, revealing potential new treatment pathways.

## Contribution

The study identifies novel gene expression patterns and biological pathways influenced by a fluorinated chalcone in TNBC cells.

## Key findings

- 504 differentially expressed genes were identified in MDA-MB-231 cells treated with a fluorinated chalcone.
- DE genes were enriched in processes like regulation of cell death and response to unfolded proteins.
- The fluorinated chalcone may influence HSF-1 silencing and promote stress-induced apoptosis.

## 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.

## Linked entities

- **Proteins:** HSF1 (heat shock transcription factor 1)
- **Chemicals:** fluorinated chalcone (PubChem CID 7946825), doxorubicin (PubChem CID 31703)
- **Diseases:** triple-negative breast cancer (MONDO:0005494), breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** HSF1 (heat shock transcription factor 1) [NCBI Gene 3297] {aka HSTF1}
- **Diseases:** TNBC (MESH:D064726)
- **Chemicals:** chalcones (MESH:D047188), Chalcone (MESH:D002599)
- **Cell lines:** MDA-MB-231 — Homo sapiens (Human), Breast adenocarcinoma, Cancer cell line (CVCL_0062)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12027753/full.md

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Source: https://tomesphere.com/paper/PMC12027753