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Sulforaphane as a Promising Natural Molecule for Cancer Prevention and Treatment
Osama A Elkashty1,2, Simon D Tran3
1McGill Craniofacial Tissue Engineering and Stem Cells Laboratory, Faculty of Dentistry, McGill University, Montreal, H3A 0G4, Canada.
Abstract:
Tumorigenicity-inhibiting compounds have been identified in our daily diet. For example, isothiocyanates (ITCs) found in cruciferous vegetables were reported to have potent cancer-prevention activities. The best characterized ITC is sulforaphane (SF). SF can simultaneously modulate multiple cellular targets involved in carcinogenesis, including (1) modulating carcinogen-metabolizing enzymes and blocking the action of mutagens; (2) inhibition of cell proliferation and induction of apoptosis; and (3) inhibition of neo-angiogenesis and metastasis. SF targets cancer stem cells through modulation of nuclear factor kappa B (NF-κB), Sonic hedgehog (SHH), epithelial-mesenchymal transition, and Wnt/β-catenin pathways. Conventional chemotherapy/SF combination was tested in several studies and resulted in favorable outcomes. With its favorable toxicological profile, SF is a promising agent in cancer prevention and/or therapy. In this article, we discuss the human metabolism of SF and its effects on cancer prevention, treatment, and targeting cancer stem cells, as well as providing a brief review of recent human clinical trials on SF.
Insights
Sulforaphane (SF), a compound from cruciferous vegetables, shows promise in cancer prevention and therapy. It targets multiple cancer pathways and stem cells, with favorable outcomes in combination studies.
Area of Science:
- Nutritional Biochemistry
- Cancer Biology
- Pharmacology
Background:
- Dietary compounds, such as isothiocyanates (ITCs) found in cruciferous vegetables, exhibit cancer-preventive properties.
- Sulforaphane (SF) is a well-characterized ITC with potent anti-cancer activities.
- SF modulates multiple targets crucial in carcinogenesis.
Purpose of the Study:
- To discuss the human metabolism of SF.
- To review SF's effects on cancer prevention, treatment, and cancer stem cell targeting.
- To provide a brief overview of recent human clinical trials involving SF.
Main Methods:
- Review of existing literature on SF metabolism and anti-cancer mechanisms.
- Analysis of SF's impact on carcinogen metabolism, cell proliferation, apoptosis, angiogenesis, and metastasis.
- Examination of SF's effects on cancer stem cell pathways (NF-κB, SHH, EMT, Wnt/β-catenin).
Main Results:
- SF modulates carcinogen-metabolizing enzymes and blocks mutagens.
- SF inhibits cell proliferation, induces apoptosis, and reduces neo-angiogenesis and metastasis.
- SF targets cancer stem cells via modulation of key signaling pathways.
Conclusions:
- SF possesses a favorable toxicological profile, making it a promising agent for cancer prevention and therapy.
- Combination therapy with conventional chemotherapy and SF has shown favorable outcomes.
- SF's multifaceted mechanisms and clinical trial data support its potential role in oncology.
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