Nanomaterial-Based Organelles Protect Normal Cells against Chemotherapy-Induced Cytotoxicity.
Ruibo ZhaoXueyao LiuXinyan YangBiao JinChangyu ShaoWeijia KangRuikang TangPublished in: Advanced materials (Deerfield Beach, Fla.) (2018)
Chemotherapy-induced cytotoxicity in normal cells and organs triggers undesired lesions. Although targeted delivery is used extensively, more than half of the chemotherapy dose still concentrates in normal tissues, especially in the liver. Enabling normal cells or organs to defend against cytotoxicity represents an alternative method for improving chemotherapy. Herein, rationally designed nanomaterials are used as artificial organelles to remove unexpected cytotoxicity in normal cells. Nanocomposites of gold-oligonucleotides (Au-ODN) can capture intracytoplasmic doxorubicin (DOX), a standard chemotherapy drug, blocking the drug's access into the cell nucleus. Cells with implanted Au-ODN are more robust since their viability is maintained during DOX treatment. In vivo experiments confirm that the Au-ODN nanomaterials selectively concentrate in hepatocytes and eliminate DOX-induced hepatotoxicity, increasing the cell's capacity to resist the threatening chemotherapeutic milieu. The finding suggests that introducing functional materials as biological devices into living systems may be a new strategy for improving the regulation of cell fate in more complex conditions and for manufacturing super cells.
Keyphrases
- induced apoptosis
- cell cycle arrest
- chemotherapy induced
- emergency department
- gene expression
- drug induced
- signaling pathway
- cell death
- multidrug resistant
- squamous cell carcinoma
- oxidative stress
- liver injury
- cell proliferation
- radiation therapy
- cell therapy
- gold nanoparticles
- sensitive detection
- reduced graphene oxide
- adverse drug
- pi k akt