Table 4.
Biomedical activity and application of sphingolipids
Subclass | Name | Activity | Medical application | Ref. |
---|---|---|---|---|
Ceramide | C6 ceramide | Increasing vincristine sensitivity via AMP activated protein kinase–p53 signaling | Colon cancer, pancreatic cancer | Chen et al., 2015 |
Oxidized graphene nanoparticles as a delivery system for the pro-apoptotic C6 ceramide | Cervical cancer | Suhrland et al., 2019 | ||
Graphene oxide nanoparticle delivery system enhance anti-cancer activity of C6 ceramide | Hepatocellular carcinoma | Wang et al., 2019 | ||
Liposomal short-chain C6 ceramide induces potent anti-osteosarcoma activity | Osteosarcoma | Zhai et al., 2015 | ||
Sphingo-myelin | Sphingomyelin | Sphingomyelin-based nanosystems (SNs) for the anticancer miRNA therapeutics | Colon cancer | Nagachinta et al., 2020 |
Site-activated drug releasing lipid-iron nanoparticle | Cancer | Medina et al., 2020 | ||
Engineered liposomes sequester bacterial exotoxins and protect from invasive infections | Antibiotics | Henry et al., 2015 | ||
Specific drug release lipid nanoparticles at infection sites | Antibiotics | Zhang et al., 2021 | ||
Glyco-sphingolipid | N-octanoyl-glucosylceramide | Improvement of doxorubicin delivery and efficacy in solid tumors | Squamous cell carcinoma, Melanoma | van Lummel et al., 2011 |
Improvement of efficacy of liposomal doxorubicin | Lobular breast carcinoma | van Hell et al., 2013 | ||
Formation of transient micro-channels within the cell membrane | Uterine sarcoma | Zalba et al., 2020 | ||
α-Galactosyl-ceramide (α-GalCer) | Antigen-presenting cell immunotherapy by the activation of endogenous iNKT cells | Non-small cell lung cancer | Toyoda et al., 2020 | |
mRNA nanovaccine with α-GalCer induces antitumor immunity by NKT cells | Melanoma | Verbeke et al., 2019 |