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Updated: Jan 23, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Effects of gossypol on apoptosis‑related gene expression in racially distinct triple‑negative breast cancer cells
Samia S Messeha1, Najla O Zarmouh1, Patricia Mendonca1
1College of Pharmacy and Pharmaceutical Science, Florida A&M University, Tallahassee, Florida 32307, USA.
Abstract:
Apoptosis is a gene‑directed mechanism that regulates cell proliferation and maintains homeostasis. Moreover, an aberrant apoptotic process can lead to several pathological conditions, such as tumorigenesis and cancer metastasis. In the present study, the apoptotic effect of the natural polyphenol compound gossypol GOSS) was investigated in triple‑negative breast cancer TNBC) cells. The effect of GOSS was evaluated in two cell lines representative of a Caucasian‑American and African‑American origin, MDA‑MB‑231 MM‑231) and MDA‑MB‑468 MM‑468), respectively. A similar response to both cytotoxicity and proliferation was observed in the two cell lines. However, MM‑468 cells were 2‑fold more sensitive to the apoptotic effect of the compound, which was accompanied by a longer delay in colony formation. Furthermore, GOSS was found to alter the mRNA expression of many apoptosis‑related genes. The compound significantly upregulated growth arrest and DNA damage‑inducible 45 alpha protein (GADD45A), tumor necrosis factor receptor superfamily 9 (TNFRSF9) and BCL2 interacting protein 3 BNIP3) in MM‑231 cells. Similarly, GADD45A and BNIP3 were upregulated in MM‑468 cells. A significant finding in this study is the profound 159‑fold increase in TNF gene expression that was observed in MM‑468 cells. Moreover, the apoptosis‑suppressor gene baculoviral IAP repeat containing 5 BIRC5) was significantly repressed (by more than 90%) in both cell lines, as well as death‑associated protein kinase 1 (DAPK1) in MM‑231 cells and tumor protein 73 (TP73) in MM‑468 cells. In conclusion, the data obtained in this study provide a molecular understanding of the GOSS‑induced apoptosis effect and suggest the importance of this polyphenol compound targeted towards TNBC treatment, particularly in African‑American women.
Insights
Gossypol induces apoptosis in triple-negative breast cancer cells, particularly those of African-American origin. This natural compound shows promise for TNBC treatment by altering key gene expressions related to cell death.
Area of Science:
- Biochemistry
- Molecular Biology
- Oncology
Background:
- Apoptosis is a crucial gene-directed process for cell proliferation and homeostasis.
- Dysregulation of apoptosis is linked to tumorigenesis and cancer metastasis.
- Triple-negative breast cancer (TNBC) presents a significant therapeutic challenge.
Purpose of the Study:
- To investigate the apoptotic effects of the natural polyphenol gossypol (GOSS) on TNBC cells.
- To compare the sensitivity and molecular response of Caucasian-American and African-American TNBC cell lines to GOSS.
- To elucidate the molecular mechanisms underlying GOSS-induced apoptosis in TNBC.
Main Methods:
- Treatment of MDA-MB-231 (Caucasian-American) and MDA-MB-468 (African-American) TNBC cell lines with gossypol.
- Assessment of cytotoxicity, proliferation, and colony formation.
- Analysis of mRNA expression levels of apoptosis-related genes using quantitative PCR.
Main Results:
- Gossypol exhibited similar cytotoxicity and proliferation inhibition in both cell lines.
- MDA-MB-468 cells showed a 2-fold higher sensitivity to GOSS-induced apoptosis.
- Gossypol modulated the expression of key apoptosis-related genes, including upregulation of GADD45A, TNFRSF9, BNIP3, and TNF, and downregulation of BIRC5, DAPK1, and TP73.
Conclusions:
- Gossypol effectively induces apoptosis in TNBC cells through modulation of specific gene expression pathways.
- The compound demonstrates differential sensitivity between TNBC cell lines of different ethnicities, with African-American cell lines being more sensitive.
- Gossypol represents a potential therapeutic agent for TNBC, especially for African-American women, warranting further investigation.
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