Nimbolide epigenetically regulates autophagy and apoptosis in breast cancer

Venkatesh Pooladanda1, Soumya Bandi2, Sandhya Rani Mondi2

  • 1Department of Regulatory Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Balanagar, Hyderabad, Telangana 500037, India.

Insights

Nimbolide, a neem compound, triggers autophagy and apoptosis in breast cancer cells, offering a potential new therapeutic strategy. This study reveals its epigenetic modifications and impact on cell proliferation.

Area of Science:

  • Biochemistry
  • Molecular Biology
  • Cancer Research

Background:

  • Autophagy is crucial for cellular balance; its disruption contributes to diseases like cancer.
  • Nimbolide, from neem, shows anticancer properties, but its role in autophagy and epigenetic changes in breast cancer is unknown.

Purpose of the Study:

  • To investigate nimbolide's potential to induce autophagy and epigenetic modifications in breast cancer.
  • To understand how nimbolide counters breast cancer progression through autophagy.

Main Methods:

  • Assessed nimbolide's effect on MDA-MB-231 and MCF-7 cell proliferation (IC50 values determined).
  • Analyzed cell cycle, mitochondrial membrane potential, and protein expression (Bcl-2, Bax, caspases, HDAC-2, H3K27Ac).
  • Utilized acridine orange, MDC, and Lysotracker Red staining for autophagolysosome visualization; quantified autophagy markers (Beclin 1, LC3B, p62, mTOR).

Main Results:

  • Nimbolide significantly inhibited breast cancer cell proliferation.
  • It induced apoptosis by altering mitochondrial membrane potential and key protein levels.
  • Nimbolide triggered autophagolysosome accumulation and modulated autophagy signaling pathways, alongside epigenetic modifications (HDAC-2, H3K27Ac).

Conclusions:

  • Nimbolide effectively induces autophagy-mediated apoptosis in breast cancer cells.
  • Epigenetic alterations play a role in nimbolide's anticancer effects.
  • Nimbolide presents a promising therapeutic agent for breast cancer, targeting both autophagy and epigenetic pathways.

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