Graphene Oxide⁻Platinum Nanoparticle Nanocomposites: A Suitable Biocompatible Therapeutic Agent for Prostate Cancer

• Published in: Polymers Vol. 11; no. 4; p. 733
• Main Authors: Gurunathan, Sangiliyandi, Jeyaraj, Muniyandi, Kang, Min-Hee, Kim, Jin-Hoi
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 23.04.2019; MDPI
• Subjects: Apoptosis; Biocompatibility; Breast cancer; Cancer therapies; Carbonyls; Cell growth; Chemical compounds; Cytotoxicity; Damage; Deoxyribonucleic acid; DNA; DNA damage; Drug dosages; Drug resistance; Gene expression; Genes; Genotoxicity; Gold; Graphene; graphene oxide–platinum nanoparticles nanocomposites; Kinases; Lactate dehydrogenase; Malondialdehyde; Membranes; Mitochondria; mitochondrial membrane potential; Mortality; Nanocomposites; Nanomaterials; Nanoparticles; Neuroblastoma; Nitric oxide; Ovarian cancer; oxidative stress; Palladium; Pharmacology; Platinum; Prostate cancer; Quantum dots; Radiation therapy; Sensors; Synthesis; Toxicity; Uric acid; Vanillin; St Louis Missouri; United States > US; prostate cancer; graphene oxide–platinum nanoparticles nanocomposites; DNA damage; cytotoxicity; oxidative stress; mitochondrial membrane potential
• ISSN: 2073-4360; 2073-4360
• DOI: 10.3390/polym11040733

Metal nanoparticles and the combination of metal nanoparticles with graphene oxide are widely used in environmental, agriculture, textile, and therapeutic applications. The effect of graphene oxide-green platinum nanoparticles (GO-PtNPs) on human prostate cancer cells (LNCaP) is unclear. Therefore, this study aimed to synthesize a nanocomposite of GO-PtNPs and evaluate their effect on prostate cancer cells. Herein, we synthesized GO-PtNPs using vanillin and characterized GO-PtNPs. GO-PtNP cytotoxicity in LNCaP cells was demonstrated by measuring cell viability and proliferation. Both decreased in a dose-dependent manner compared to that by GO or PtNPs alone. GO-PtNP cytotoxicity was confirmed by increased lactate dehydrogenase release and membrane integrity loss. Oxidative stress induced by GO-PtNPs increased malondialdehyde, nitric oxide, and protein carbonyl contents. The effective reactive oxygen species generation impaired the cellular redox balance and eventually impaired mitochondria by decreasing the membrane potential and ATP level. The cytotoxicity to LNCaP cells was correlated with increased expression of proapoptotic genes (p53, p21, Bax, Bak, caspase 9, and caspase 3) and decreased levels of antiapoptotic genes (Bcl2 and Bcl-xl). Activation of the key regulators p53 and p21 inhibited the cyclin-dependent kinases Cdk2 and Cdk4, suggesting that p53 and p21 activation in GO-PtNP-treated cells caused genotoxic stress and apoptosis. The increased expression of genes involved in cell cycle arrest and DNA damage and repair, and increased levels of 8-oxo-deoxyguanosine and 8-oxoguanine suggested that GO-PtNPs potentially induce oxidative damage to DNA. Thus, GO-PtNPs are both cytotoxic and genotoxic. LNCaP cells appear to be more susceptible to GO-PtNPs than to GO or PtNPs. Therefore, GO-PtNPs have potential as an alternate and effective cancer therapeutic agent. Finally, this work shows that the combination of graphene oxide with platinum nanoparticles opens new perspectives in cancer therapy. However further detailed mechanistic studies are required to elucidate the molecular mechanism of GO-PtNPs induced cytotoxicity in prostate cancer.