The Cytotoxicity of Carbon Nanotubes and Hydroxyapatite, and Graphene and Hydroxyapatite Nanocomposites against Breast Cancer Cells.
Tristan NguyenAnuj ManiyarMrinmoy SarkarTapasree Roy SarkarGururaj M NeelgundPublished in: Nanomaterials (Basel, Switzerland) (2023)
Cancer is a current dreadful disease and the leading cause of death. Next to cardiovascular diseases, cancer is the most severe threat to human life and health. Breast cancer is the most common invasive cancer diagnosed in women. Each year about 2.3 million women are diagnosed with breast cancer. In consideration of the severity of breast cancer, herein we designed the biocompatible nanomaterials, CNTs-HAP and GR-HAP, through grafting of hydroxyapatite (HAP) to carbon nanotubes (CNTs) and graphene (GR) nanosheets. CNTs-HAP and GR-HAP have been tested for their cytotoxicity, growth and motility inhibitory effects, and their effects on the mesenchymal markers. All these demonstrated significant dose-dependent and time-dependent in vitro cytotoxicity against SUM-159 and MCF-7 breast cancer cell lines. The cell viability assay showed that the CNTs-HAP was more effective over SUM-159 cells than MCF-7 cells. It found that the increase in the concentration of GR-HAP has inhibited the clonogenic ability of breast cancer cells. The GR-HAP exhibited a substantial inhibitory effect on the cell motility of SUM-159 cell lines. It was investigated that the expression of vimentin (mesenchymal marker) was majorly reduced in SUM-159 cells by GR-HAP.
Keyphrases
- carbon nanotubes
- breast cancer cells
- induced apoptosis
- papillary thyroid
- cell cycle arrest
- cardiovascular disease
- stem cells
- squamous cell
- breast cancer risk
- childhood cancer
- polycystic ovary syndrome
- healthcare
- public health
- endothelial cells
- poor prognosis
- type diabetes
- escherichia coli
- coronary artery disease
- mental health
- ionic liquid
- early onset
- high resolution
- pregnancy outcomes
- lymph node metastasis
- skeletal muscle
- bone regeneration
- drug delivery
- staphylococcus aureus
- single molecule
- pluripotent stem cells
- binding protein