Date Pit Carbon Dots Induce Acidic Inhibition of Peroxidase and Disrupt DNA Repair in Antibacteria Resistance.
Ayan A NurkeshQinglei SunHaiyan FanKanat DukenbayevAndrey TsoyAkerke AltaikyzyKunjie WangYingqiu XiePublished in: Global challenges (Hoboken, NJ) (2019)
Carbon nanodots (C-dots) are emerging as a new type of promising agent in anticancer, imaging, and new energy. Reports as well as the previous research indicate that certain C-dots can enhance targeted cancer therapy. However, in-depth mechanisms for such anticancer effect remain unclear. In this work, treatment provided by the date pit-derived C-dots, exhibits significant DNA damage; Annexin V/7-AAD-mediated apoptosis, and G2/M cell cycle arrest in prostate cancer cells. The application of C-dots to the cell generally leads to acidulation of the cell medium, cooperated with membrane compact. The date pit-derived C-dots are observed inhibiting the horseradish peroxidase. Moreover, the C-dots disrupt likely through nucleotide excision DNA repair at low dose during DNA ligation step suggesting the antimicrobial effect and targeting Pim-1, EGFR, mTOR, and DNA damage pathways in cancer cells. For the first time the detailed and novel mechanisms underlying the C-dots, derived from the date-pit, as an efficient, low-cost, and green nanomaterial are reveled for cancer therapy and anti-infection.
Keyphrases
- dna repair
- dna damage
- cancer therapy
- fluorescent probe
- molecularly imprinted
- low dose
- low cost
- drug delivery
- oxidative stress
- dna damage response
- cell cycle arrest
- single cell
- cell death
- high resolution
- cell therapy
- emergency department
- stem cells
- photodynamic therapy
- ionic liquid
- pi k akt
- tyrosine kinase
- cell free
- mesenchymal stem cells