The natural compound Alizarin as an osteotropic drug for the treatment of bone tumors

Research output: Contribution to journalArticlepeer-review

Abstract

Despite significant clinical improvements, conventional therapies for bone cancer treatment are limited by significant systemic toxicity and lack of specific targeting. In this study, we considered Alizarin, a natural hydroxyanthraquinone derived from madder root with high affinity to calcium and remarkable osteotropic features, as a novel approach for bone cancer treatment. Due to its antitumor properties, as demostrated in colon cancer cells, and to its tropism to bone, Alizarin may be an ideal drug to reduce bone tumor growth. We demonstrated that low dosages of Alizarin strongly inhibited the osteosarcoma (IC 50 for Saos-2, MG-63, and U-2 OS cells, 27.5, 29.0, and 69.9μg/ml, respectively) and breast carcinoma (IC 50 for MDA-MB-231 cells, 62.1μg/ml) cell proliferation in vitro. Importantly, Alizarin had a significantly lower inhibitory activity on normal cells (IC 50 for MSC, 828.6μg/ml), thereby revealing a selective activity towards malignant cells. Furthermore, we found that Alizarin acted through the inhibition of ERK phosphorylation and cell cycle arrest in the S-phase. Finally, Alizarin significantly and strongly impaired both osteosarcoma and breast cancer tumorigenesis. Our results highlight a selective and effective inhibitory activity of Alizarin towards cancerous cells, laying the basis for further studies to investigate its application in bone cancer therapy.

Original languageEnglish
Pages (from-to)1486-1492
Number of pages7
JournalJournal of Orthopaedic Research
Volume30
Issue number9
DOIs
Publication statusPublished - Sep 2012

Keywords

  • alizarin
  • anthraquinone
  • bone tumors
  • cell cycle
  • osteotropism

ASJC Scopus subject areas

  • Orthopedics and Sports Medicine

Fingerprint Dive into the research topics of 'The natural compound Alizarin as an osteotropic drug for the treatment of bone tumors'. Together they form a unique fingerprint.

Cite this