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Gercumin synergizes the action of 5-fluorouracil and oxaliplatin against chemoresistant human cancer colon cells

Authors :
Pratima Nangia-Makker
Francesca Preziuso
Serena Fiorito
Adhip P.N. Majumdar
Salvatore Genovese
Francesco Epifano
Jill Slater
Source :
Biochemical and Biophysical Research Communications. 522:95-99
Publication Year :
2020
Publisher :
Elsevier BV, 2020.

Abstract

Advanced colon cancer is extremely difficult to cure, underscoring the need to develop novel therapeutic agents. Prenylated curcumins that are semisynthetic curcumin derivatives with significant anti-cancer potential have been studied herein to assess their therapeutic potential for colon cancer and tested to this aim in vitro for their growth inhibitory properties against 5-fluorouracil + oxaliplatin resistant human colon cancer CR-HT29 and HCT-116 cells. The resulting most active product, gercumin (mono-O-geranylcurcumin), has been further tested for its synergistic effects with FOLFOX (a combination of 5-fluorouracil and oxaliplatin) on the same cell lines. Activity of this combination on colonosphere formation was also investigated. Gercumin was able to suppress the growth of cancer cells with a potency similar to that of curcumin. A synergistic effect of this compound and FOLFOX was also observed. doses tested for synergy in the colonosphere assays did not show greater suppression of colonosphere formation than independent treatment with either reagent alone. Only one of the combinations was shown to be more effective at suppressing colonosphere formation [gercumin 5 μM + FOLFOX (2x)]. Thus, the growth inhibitory effects of curcumin against human cancer cells can be modulated and enhanced by the introduction of hydrophobic chains, normally found in several natural compounds, like the geranyl one. Such compounds are also able to synergize with known chemotherapeutics.

Details

ISSN :
0006291X
Volume :
522
Database :
OpenAIRE
Journal :
Biochemical and Biophysical Research Communications
Accession number :
edsair.doi.dedup.....1bc54624842078f48ebc119605904ff3
Full Text :
https://doi.org/10.1016/j.bbrc.2019.11.068