Cordycepin-loaded Nanoparticles from Cassava Starch Promote the Proliferation of Submandibular Gland Cells and Inhibit the Growth of Oral Squamous Carcinoma Cells.
Palakorn KaokaenAtchara JaiboonmaNipha ChaicharoenaudomrungPhongsakorn KunhormKajohnkiart JanebodinParinya NoisaPaiboon JitprasertwongPublished in: Nutrition and cancer (2020)
This study examined associations between the effect of treatment with nano-cassava starch that contained cordycepin (CS) extract, targeting human submandibular gland cells (HSGs), and human oral squamous carcinoma cells (HSC-4). Cassava starch nanoparticles (CSNPs) were prepared by either physical or acid treatment. These nanoparticles were then loaded with either CS or cordyceps medium and then treated with HSG or HSC-4 cells in different concentrations of CS and nanoparticles. Moreover, the protein secretion, reactive oxygen species (ROS) activity and the expression of salivary-specific genes, antioxidant gene were determined after treatment. CSNPs can enhance the activity of CS at low concentrations. Cordycepin-loaded cassava starch nanoparticles (CCSNPs) increased HSG proliferation, protein secretion, and the expression of salivary-specific genes, AMY and AQP5. Besides, CCSNPs also protected and scavenged of ROS via the stimulation of the antioxidant genes in HSGs, indicating the protective roles of CS to HSGs. On the other hand, CCSNPs inhibited the growth of HSC-4 cells by stimulating ROS generation and reducing protein secretion. This finding suggested that CCSNPs presented the dual actions against HSGs and human oral squamous carcinoma cells, and the encapsulation of CS with cassava nanoparticles enhanced the activity of CS.
Keyphrases
- induced apoptosis
- cell cycle arrest
- reactive oxygen species
- endothelial cells
- cell death
- drug delivery
- signaling pathway
- genome wide
- cancer therapy
- high grade
- dna damage
- endoplasmic reticulum stress
- binding protein
- physical activity
- small molecule
- induced pluripotent stem cells
- anti inflammatory
- amino acid
- pi k akt
- copy number
- protein protein
- combination therapy
- long non coding rna
- genome wide analysis