| Literature DB >> 32825600 |
Natalia Miękus1, Krystian Marszałek2,3, Magdalena Podlacha4, Aamir Iqbal5, Czesław Puchalski6, Artur H Świergiel7,8.
Abstract
The broad spectrum of the mechanism of action of immune-boosting natural compounds as well as the complex nature of the food matrices make researching the health benefits of various food products a complicated task. Moreover, many routes are involved in the action of most natural compounds that lead to the inhibition of chronic inflammation, which results in a decrease in the ability to remove a pathogen asymptomatically and is connected to various pathological events, such as cancer. A number of cancers have been associated with inflammatory processes. The current review strives to answer the question of whether plant-derived sulfur compounds could be beneficial in cancer prevention and therapy. This review focuses on the two main sources of natural sulfur compounds: alliaceous and cruciferous vegetables. Through the presentation of scientific data which deal with the study of the chosen compounds in cancer (cell lines, animal models, and human studies), the discussion of food processing's influence on immune-boosting food content is presented. Additionally, it is demonstrated that there is still a need to precisely demonstrate the bioavailability of sulfur-containing compounds from various types of functional food, since the inappropriate preparation of vegetables can significantly reduce the content of beneficial sulfur compounds. Additionally, there is an urgent need to carry out more epidemiological studies to reveal the benefits of several natural compounds in cancer prevention and therapy.Entities:
Keywords: alliaceous vegetables; cruciferous vegetables; food processing; functional food; nutraceuticals; sulfur-based compounds
Mesh:
Substances:
Year: 2020 PMID: 32825600 PMCID: PMC7503525 DOI: 10.3390/molecules25173804
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411
Figure 1Glucosinolate classification based on the structure of their amino acid precursors. Among the common amino acid precursors of glucosinolates are aromatic amino acids, phenylalanine, or tyrosine; aliphatic amino acids include alanine, leucine, isoleucine, methionine, and valine, whereas indole glucosinolates are those derived from tryptophan.
Figure 2Breakdown of glucosinolates and the possible alternative breakdown products.
Health-promoting role of Glucosinolate.
| Glucosinolate | Type of Compound | Health Promoting Roles and Plant Protection | Reference |
|---|---|---|---|
| Sulforaphane | Isothiocyanates | Inhibition of transcription regulator (NF-κB), which is relevant against inflammation and for minimizing diabetes-related complications such as diabetic neuropathy. | [ |
| Mediation of cell cycle arrest and apoptosis; inhibition of the activity of histone deacetylase; and increasing histone acetylation, which leads to the enhancement of protection against carcinogenesis. | [ | ||
| Normalization of kidney genome and blood pressure owing to the decrease in oxidative stress in cardiovascular and kidney tissues. | [ | ||
| Decreasing infarct size, brain edema, and cortical apoptosis, reducing the inflammation and tissue damage of the central nervous system due to the activation of the transcription factor Nrf2, and the upregulation of different target genes. | [ | ||
| Reduction in the damage induced by high concentrations of substances that mimic the pathomechanism of autism spectrum disorders in mice models. | [ | ||
| Treatment of | [ | ||
| Reduces the risk of skin lesions caused by UV radiation, especially in high-risk patients. | [ | ||
| Glucoiberin, Sinigrin, and Progoitrin | Suppressing agents, protection of human and animal cells against carcinogenesis owing to the induction of Phase II detoxification enzymes or the inhibition of Phase I enzymes. | [ | |
| Indole-3-Carbinol | Chemopreventive agent. | [ | |
| Benzyl Isothiocyanate | Bactericidal and fungicidal properties and has proven effective in combating respiratory and urinary tract infections. | [ | |
| Chemopreventive agent. | [ | ||
| Allyl Isothiocyanate, Allyl Thiocyanate, and Allyl Isocyanate | Effective natural insecticides, efficiency in eliminating nematodes or flying insects. Possible mechanisms: the inhibition of the activity of the thiol groups of key enzymes, or the blocking of electron transport and ATP synthesis. | [ |
Figure 3Organosulfur compounds and possible reactions of allicin.
Metabolic role of different organo-sulfur compounds in the human body.
| Organosulfur Compound | Type of Compound | Health Promoting Role | Reference |
|---|---|---|---|
| Alliin (S-Allylcysteine Sulfoxide) | Natural bioactive constituent, with general formula C6H11NO3S. | It modulates the generation of proinflammatory cytokines by increasing the expression of cytokine genes like IL-6, MCP-1, and EGR-1. It also shows strong antioxidant and radical-scavenging properties. Alliin has also been found to boost the immune response in blood. | [ |
| Allicin | Thiosulfinate and also the precursor of various sulfur-containing compounds, with the general formula C6H10OS2. | Allicin exhibits anti-cancer, anti-bacterial, anti-fungal, and anti-tumor activities. Allicin can inhibit the proliferation of tumor cells and can induce apoptosis in gastric cells by activating both the intrinsic and extrinsic pathways. Allicin shows anti-bacterial effects against a wide range of Gram-negative and Gram-positive bacteria (Staphylococcus, Escherichia, Klebsiella, Salmonella, Bacillus, Streptococcus, Proteus, and Clostridium). Moreover, allicin can also stimulate cytokine release, enhance immune resistance, and has anti-parasitic activity against several parasites. | [ |
| Sulfenic Acid | First member of the family of organosulfur oxoacids, with the general formula RSOH. | Upon the chopping, damage, chewing, or crushing of Allium plants, the enzyme alliinase catalyzes the decomposition of alliin into short-lived and unstable sulfenic acid. It is thought to be responsible for antioxidant activities. | [ |
| Diallyl Sulfide (DAS) | Derived bioactive compound which is a lipophilic thioether, with the general formula C6H10S. | Diallyl sulfide can boost the detoxification functions of liver cells, preventing symptoms of inflammation. It significantly enhances the production of the enzyme glutathione S-transferase (GST), which binds the electrophilic toxins inside the cell. DAS can inhibit the activation of nicotine-derived nitrosamine ketone (NNK), which is related to carcinogenesis. The preventive treatment with DAS also decreases the acetaminophen-induced hepatotoxicity and nephrotoxicity, indicating that it can decrease liver damage induced by drugs. It is also found to be effective against cardiovascular disease and colon cancer. | [ |
| Diallyl Disulfide (DADS) | Derived organosulfur compound with the general formula C6H10S2. | Diallyl disulfide has multitargeted anti-carcinogenic activities, by (1) promoting carcinogen metabolism, (2) retarding the progression of the cell cycle, (3) inhibiting the proliferation of cells and inducing apoptosis. Moreover, diallyl disulfide also inhibit histone deacetylase activities, which have a therapeutic effect to stop cancer, since it can modulate histone hyper-acetylation and can reactivate tumor suppressor genes involved in cancer progression. Besides these benefits, it can induce allergens in | [ |
| Allitridin or Diallyl | Derived organosulfur compound with the formula C6H10S3. | Diallyl trisulfide have several health-promoting benefits, including having anti-cancer properties, being an antiviral immune booster, causing an increase in the reactive oxygen species (ROS) level, causing platelet aggregation, causing a decrease in blood pressure, causing cholesterol reduction, and being helpful in the treatment of cardiac arrhythmias. It has been found to selectively kill the cancerous cells in the breast and prostate, leaving the healthy cells unharmed. | [ |