Gene Expression and Transcriptome Profiling of Changes in a Cancer Cell Line Post-Exposure to Cadmium Telluride Quantum Dots: Possible Implications in Oncogenesis.
Mohammed S AldughaimMashael R Al-AnaziMarie Fe F BoholDilek ColakHani AlothaidSalma Majid WakilSamya T HagosDaoud AliSaud AlarifiSashmita RoutSaad AlkahtaniMohammed N Al-AhdalAhmed A Al-QahtaniPublished in: Dose-response : a publication of International Hormesis Society (2021)
Cadmium telluride quantum dots (CdTe-QDs) are acquiring great interest in terms of their applications in biomedical sciences. Despite earlier sporadic studies on possible oncogenic roles and anticancer properties of CdTe-QDs, there is limited information regarding the oncogenic potential of CdTe-QDs in cancer progression. Here, we investigated the oncogenic effects of CdTe-QDs on the gene expression profiles of Chang cancer cells. Chang cancer cells were treated with 2 different doses of CdTe-QDs (10 and 25 μg/ml) at different time intervals (6, 12, and 24 h). Functional annotations helped identify the gene expression profile in terms of its biological process, canonical pathways, and gene interaction networks activated. It was found that the gene expression profiles varied in a time and dose-dependent manner. Validation of transcriptional changes of several genes through quantitative PCR showed that several genes upregulated by CdTe-QD exposure were somewhat linked with oncogenesis. CdTe-QD-triggered functional pathways that appear to associate with gene expression, cell proliferation, migration, adhesion, cell-cycle progression, signal transduction, and metabolism. Overall, CdTe-QD exposure led to changes in the gene expression profiles of the Chang cancer cells, highlighting that this nanoparticle can further drive oncogenesis and cancer progression, a finding that indicates the merit of immediate in vivo investigation.
Keyphrases
- quantum dots
- genome wide
- gene expression
- genome wide identification
- cell cycle
- sensitive detection
- cell proliferation
- copy number
- dna methylation
- papillary thyroid
- transcription factor
- energy transfer
- genome wide analysis
- heavy metals
- healthcare
- squamous cell carcinoma
- risk assessment
- molecularly imprinted
- late onset
- escherichia coli
- lymph node metastasis
- oxidative stress
- mass spectrometry
- childhood cancer
- health information
- staphylococcus aureus
- cystic fibrosis
- simultaneous determination
- social media