Clerodendrum chinense Stem Extract and Nanoparticles: Effects on Proliferation, Colony Formation, Apoptosis Induction, Cell Cycle Arrest, and Mitochondrial Membrane Potential in Human Breast Adenocarcinoma Breast Cancer Cells

Int J Mol Sci. 2024 Jan 12;25(2):978. doi: 10.3390/ijms25020978.

Abstract

Breast cancer stands out as the most widespread form of cancer globally. In this study, the anticancer activities of Clerodendrum chinense (C. chinense) stem ethanolic extract were investigated. High-performance liquid chromatography (HPLC) analysis identified verbascoside and isoverbascoside as the major bioactive compounds in the C. chinense stem extract. Successfully developed nanoparticles exhibited favorable hydrodynamic diameter, polydispersity index, and surface charge, thus ensuring stability after four months of storage. The total phenolic content and total flavonoid contents in the nanoparticles were reported as 88.62% and 95.26%, respectively. The C. chinense stem extract demonstrated a dose-dependent inhibitory effect on MCF-7, HeLa, A549, and SKOV-3 cancer cell lines, with IC50 values of 109.2, 155.6, 206.9, and 423 µg/mL, respectively. C. chinense extract and NPs exhibited dose-dependent cytotoxicity and the highest selectivity index values against MCF-7 cells. A dose-dependent reduction in the colony formation of MCF-7 cells was observed following treatment with the extract and nanoparticles. The extract induced cytotoxicity in MCF-7 cells through apoptosis and necrosis. C. chinense stem extract and nanoparticles decreased mitochondrial membrane potential (MMP) and induced G0/G1 phase arrest in MCF-7 cells. In conclusion, use of C. chinense stem extract and nanoparticles may serve as a potential therapeutic approach for breast cancer, thus warranting further exploration.

Keywords: anticancer; breast cancer; nanoparticles; plant extract; polyphenol.

MeSH terms

  • Adenocarcinoma*
  • Apoptosis
  • Breast Neoplasms* / drug therapy
  • Cell Cycle Checkpoints
  • Cell Proliferation
  • Clerodendrum*
  • Female
  • HeLa Cells
  • Humans
  • Membrane Potential, Mitochondrial
  • Plant Extracts / pharmacology

Substances

  • Plant Extracts

Grants and funding

This research was funded by Chiang Mai University grant number RG01/2566 and The APC was funded by the Center of Excellence in Pharmaceutical Nanotechnology, Chiang Mai University.