Sanguinarine cytotoxicity on mouse melanoma K1735-M2 cells-Nuclear vs. mitochondrial effects

Teresa L. Serafim, Júlio A.C. Matos, Vilma A. Sardão, Gonçalo C. Pereira, Ana F. Branco, Sandro L. Pereira, Donna Parke, Edward L. Perkins, António J.M. Moreno, Jon M Holy, Paulo J. Oliveira

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45 Scopus citations


Sanguinarine (SANG) is an alkaloid recognized to have anti-proliferative activity against various human tumour cell lines. No data is available on the susceptibility of advanced malignant melanoma to SANG, although this disease has a very poor prognosis if not detected in time due to the resistance to conventional chemotherapy. The present work was designed to study the nuclear and mitochondrial involvement in the pro-apoptotic effect of SANG in an invasive mouse melanoma cell line. The results obtained show that SANG is primarily accumulated by the cell nuclei, causing inhibition of cell proliferation and inducing cell death, as confirmed by an increase in sub-G1 peaks. At low concentrations, SANG induces mitochondrial depolarization in a sub-population of melanoma cells, which also generally displayed strong nuclear labelling of phosphorylated histone H2AX. Western blotting revealed an increase in p53, but not Bax protein, in both whole-cell extracts and in mitochondrial fractions. Isolated hepatic mitochondrial fractions revealed that SANG affects the mitochondrial respiratory chain, and has dual effects on mitochondrial calcium loading capacity. We suggest that SANG is able to induce apoptosis in metastatic melanoma cells. The knowledge of mitochondrial vs. nuclear effects of SANG is important in the development of this promising compound for clinical use against aggressive melanoma.

Original languageEnglish (US)
Pages (from-to)1459-1475
Number of pages17
JournalBiochemical Pharmacology
Issue number11
StatePublished - Dec 1 2008

Bibliographical note

Funding Information:
The present work was funded by the Portuguese Foundation for Science and Technology (FCT), research grant PTDC/SAU/OSM/64084/2006. FCT also supported TLS (Ph.D. fellowship SFRH/BD/38067/2007), VAS (Pos-Doc fellowship SFRH/BPD/31549/2006), GCP (Ph.D. fellowship SFRH/BD/36938/2007), AFB (Ph.D. fellowship SFRH/BD/41384/2007) and SLP (Ph.D. fellowship SFRH/BD/37933/2007).


  • Apoptosis
  • Bioenergetics
  • Cell proliferation
  • K1735-M2 rat melanoma cells
  • Liver mitochondria
  • Mitochondrial permeability transition
  • Mitochondrial physiology
  • Sanguinarine


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