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Cancer Chemotherapy and Pharmacology

, Volume 64, Issue 1, pp 201–211 | Cite as

Do anthocyanins and anthocyanidins, cancer chemopreventive pigments in the diet, merit development as potential drugs?

  • Sarah Thomasset
  • Nicole Teller
  • Hong Cai
  • Doris Marko
  • David P. Berry
  • William P. Steward
  • Andreas J. Gescher
Commentary

Abstract

Anthocyanins, plant pigments in fruits and berries, have been shown to delay cancer development in rodent models of carcinogenesis, especially those of the colorectal tract. Anthocyanins and anthocyanidins, their aglycons, especially cyanidin and delphinidin, have been subjected to extensive mechanistic studies. In cells in vitro, both glycosides and aglycons engage an array of anti-oncogenic mechanisms including anti-proliferation, induction of apoptosis and inhibition of activities of oncogenic transcription factors and protein tyrosine kinases. Anthocyanins and anthocyanidins exist as four isomers, interconversion between which depends on pH, temperature and access to light. Anthocyanidins are much more prone to avid chemical decomposition than the glycosides, and they only survive for minutes in the biophase. These pharmaceutical issues are very important determinants of the suitability of these flavonoids for potential development as cancer chemopreventive drugs, and they have hitherto not received adequate attention. In the light of their robust cancer chemopreventive efficacy in experimental models and their superior stability as compared to that of the aglycons, the anthocyanins seem much more suitable for further drug development than their anthocyanidin counterparts.

Keywords

Cancer chemoprevention Anthocyanins Drug development 

Notes

Acknowledgments

The work in the Karlsruhe and Leicester groups is supported by a grant from the FlavoNet initiative of the Deutsche Forschungsgemeinschaft and a programme grant from Cancer Research UK.

Conflict of interest statement

None.

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Copyright information

© Springer-Verlag 2009

Authors and Affiliations

  • Sarah Thomasset
    • 1
  • Nicole Teller
    • 2
  • Hong Cai
    • 1
  • Doris Marko
    • 2
  • David P. Berry
    • 3
  • William P. Steward
    • 1
  • Andreas J. Gescher
    • 1
  1. 1.Cancer Biomarkers and Prevention Group, Department of Cancer Studies and Molecular Medicine, RKCSB, LRIUniversity of LeicesterLeicesterUK
  2. 2.Section of Food Toxicology, Institute of Applied BiosciencesUniversität Karlsruhe (TH)KarlsruheGermany
  3. 3.Department of Hepatobiliary and Pancreatic SurgeryLeicester General Hospital, University Hospitals of LeicesterLeicesterUK

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