Carcinogenesis 2015-03-01

Curcumin mediates chemosensitization to 5-fluorouracil through miRNA-induced suppression of epithelial-to-mesenchymal transition in chemoresistant colorectal cancer.

Shusuke Toden, Yoshinaga Okugawa, Thomas Jascur, Dominik Wodarz, Natalia L Komarova, Constanze Buhrmann, Mehdi Shakibaei, C Richard Boland, Ajay Goel

Index: Carcinogenesis 36(3) , 355-67, (2015)

Full Text: HTML

Abstract

Resistance to cytotoxic chemotherapy is a major cause of mortality in colorectal cancer (CRC) patients. Chemoresistance has been linked primarily to a subset of cancer cells undergoing epithelial-mesenchymal transition (EMT). Curcumin, a botanical with antitumorigenic properties, has been shown to enhance sensitivity of cancer cells to chemotherapeutic drugs, but the molecular mechanisms underlying this phenomenon remain unclear. Effects of curcumin and 5-fluorouracil (5FU) individually, and in combination, were examined in parental and 5FU resistant (5FUR) cell lines. We performed a series of growth proliferation and apoptosis assays in 2D and 3D cell cultures. Furthermore, we identified and analyzed the expression pattern of a subset of putative EMT-suppressive microRNAs (miRNAs) and their downstream target genes regulated by curcumin. Chemosensitizing effects of curcumin were validated in a xenograft mouse model. Combined treatment with curcumin and 5FU enhanced cellular apoptosis and inhibited proliferation in both parental and 5FUR cells, whereas 5FU alone was ineffective in 5FUR cells. A group of EMT-suppressive miRNAs were upregulated by curcumin treatment in 5FUR cells. Curcumin suppressed EMT in 5FUR cells by downregulating BMI1, SUZ12 and EZH2 transcripts, key mediators of cancer stemness-related polycomb repressive complex subunits. Using a xenograft and mathematical models, we further demonstrated that curcumin sensitized 5FU to suppress tumor growth. We provide novel mechanistic evidence for curcumin-mediated sensitization to 5FU-related chemoresistance through suppression of EMT in 5FUR cells via upregulation of EMT-suppressive miRNAs. This study highlights the potential therapeutic usefulness of curcumin as an adjunct in patients with chemoresistant advanced CRC. © The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.


Related Compounds

  • Curcumin
  • toluidine blue for...

Related Articles:

Mucoadhesive films containing chitosan-coated nanoparticles: a new strategy for buccal curcumin release.

2014-11-01

[J. Pharm. Sci. 103(11) , 3764-71, (2014)]

Enhancing the anti-inflammatory activity of chalcones by tuning the Michael acceptor site.

2015-03-14

[Org. Biomol. Chem. 13(10) , 3040-7, (2015)]

An antifungal mechanism of curcumin lies in membrane-targeted action within Candida albicans.

2014-11-01

[IUBMB Life 66(11) , 780-5, (2015)]

Identification of the cellular mechanisms that modulate trafficking of frizzled family receptor 4 (FZD4) missense mutants associated with familial exudative vitreoretinopathy.

2014-06-01

[Invest. Ophthalmol. Vis. Sci. 55(6) , 3423-31, (2014)]

Improved plasma membrane expression of the trafficking defective P344R mutant of muscle, skeletal, receptor tyrosine kinase (MuSK) causing congenital myasthenic syndrome.

2015-03-01

[Int. J. Biochem. Cell Biol. 60 , 119-29, (2015)]

More Articles...