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Galangin promotes apoptosis by upregulating the pro-apoptotic gene BAX in triple-negative breast cancer
Shruti Sinnarkar1, Poonam Suryawanshi2, Amol Dilip3
1Dr. D. Y. Patil Biotechnology & Bioinformatics Institute, Dr. D. Y. Patil Vidyapeeth, Tathawade, Pune, India.
Background:
Triple-negative breast cancer (TNBC) is one of the most aggressive and formidable subtypes of breast cancer, devoid of targeted therapy and frequently leading to unfavorable prognoses and significant side effects. The demand for creative and effective treatment options has prompted the current study to investigate the potential of natural chemicals as therapeutic agents. This study intends to examine the efficacy of Galangin, a naturally occurring flavonoid, in treating triple-negative breast cancer.
Methods:
The research utilizes a dual methodology, combining in silico network pharmacology with in vitro experimental methods. The in silico research proved crucial in finding significant gene targets and cellular signaling pathways influenced by Galangin in triple-negative breast cancer. To corroborate these computational predictions, a variety of in vitro studies were conducted, including the MTT assay, wound scratch assay, apoptosis assay, reactive oxygen species assay, mitochondrial membrane potential assessment, and RT-PCR.
Results:
Fifteen prevalent genes were identified, demonstrating involvement in cellular proliferation, apoptosis regulation, cell migration, MAPK cascade regulation, and cell cycle regulation. The predominant genes implicated in the ten principal pathways were MAPK1, MAPK8, MAPK14, and IL6, which were observed to be linked to the MAPK signaling pathway, perhaps serving as the critical channel through which Galangin may facilitate the treatment of oral cancer. In vitro experiments demonstrated anti-proliferative effects, late-stage apoptosis, anti-migratory characteristics, antioxidant activity, and upregulation of the pro-apoptotic BAX gene.
Conclusion:
This study's results demonstrate that Galangin possesses considerable anti-proliferative effects on TNBC cells, underscoring its potential as a viable therapeutic drug. These findings facilitate the development of more effective and precisely focused therapy approaches for TNBC, providing optimism for enhanced treatment outcomes for patients suffering from this challenging disease.
Insights
Galangin, a natural flavonoid, shows significant anti-cancer effects against triple-negative breast cancer (TNBC). This study reveals its potential to inhibit proliferation and induce apoptosis, offering new therapeutic avenues for TNBC treatment.
Area of Science:
- Oncology
- Natural Product Chemistry
- Molecular Biology
Background:
- Triple-negative breast cancer (TNBC) is an aggressive subtype lacking targeted therapies, necessitating novel treatment strategies.
- Natural compounds are being explored for their therapeutic potential against challenging cancers.
- Galangin, a flavonoid, is investigated for its efficacy in treating TNBC.
Purpose of the Study:
- To evaluate the therapeutic potential of Galangin against triple-negative breast cancer.
- To identify molecular targets and pathways affected by Galangin in TNBC cells.
Main Methods:
- Combined in silico network pharmacology and in vitro experimental approaches.
- In silico analysis identified key gene targets and signaling pathways.
- In vitro assays included MTT, wound scratch, apoptosis, ROS, mitochondrial membrane potential, and RT-PCR.
Main Results:
- Identified 15 key genes involved in proliferation, apoptosis, migration, and cell cycle regulation.
- MAPK signaling pathway, involving MAPK1, MAPK8, MAPK14, and IL6, emerged as a critical target.
- In vitro studies confirmed Galangin's anti-proliferative, pro-apoptotic, anti-migratory, and antioxidant effects, with BAX gene upregulation.
Conclusions:
- Galangin exhibits significant anti-proliferative effects on TNBC cells.
- It holds promise as a potential therapeutic agent for TNBC.
- Findings support the development of targeted therapies for TNBC, improving patient outcomes.
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