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ABSTRACT
Sulforaphane (SFN), a naturally occurring chemopreventive and anticancer agent, is a nuclear factor, erythroid 2-like 2 (NFE2L2/Nrf2) inducer. Nrf2 plays a critical role in coordinating the cell defense system by initiating the transcription of cytoprotective genes, including detoxification enzymes such as NAD(P)H quinone dehydrogenase 1 (NQO1) and transport proteins such as ATP-binding cassette, subfamily C (CFTR/MRP). Recently, the essential role of Nrf2 in tumor development and progression and in the development of multidrug resistance in cancer cells has been highlighted. The aim of this study was to compare the effect of SFN on the Nrf2 system and the Nrf2-target enzymes NQO1 and MRP in human untransformed epithelial colon CRL-1790 cells and in HT-29 and Caco-2 colorectal cancer cells to elucidate the role of SFN in cancer prevention and treatment. We have demonstrated that SFN has excellent cytoprotective properties in CRL-1790 cells, as it induced Nrf2-dependent expression of MRP1 and NQO1. SFN induced Nrf2 target enzyme activity in HT-29 and Caco-2 cancer cells but regulated the Nrf2/ARE signaling pathway differently in cancer and untransformed cells.
Abbreviations
| Nrf2 | = | nuclear factor, erythroid 2-like 2 |
| SFN | = | sulforaphane |
| ITCs | = | isothiocyanates |
| NQO1 | = | NAD(P)H quinone dehydrogenase 1 |
| MRP | = | ATP-binding cassette, subfamily C |
| MDR | = | multidrug resistance |
| ARE | = | antioxidant response element |
| Keap1 | = | Kelch-like ECH-associated protein 1 |
Acknowledgments
This research was supported by institutional funding DS 3.12 from the National Medicines Institute, Warsaw, Poland.