Evaluating Single-Cell DNA Damage Induced by Enhanced Radiation on a Gold Nanofilm Patch.
Yong QiaoYuanshuai ZhouTongqian XiaoZhiwei ZhangLiyuan MaMing SuGuangli SuoPublished in: ACS applied materials & interfaces (2017)
Although radiotherapy is a general oncology treatment and is often synergistically applied with surgery and chemotherapy, it can cause side effects during and after treatment. Gold nanoparticles were studied as a potential material to enhance radiation to induce damage in cancer cells. However, few studies have been conducted to examine the effects of gold nanofilm on cell impairment under X-ray treatment. This paper describes a microfabrication-based single-cell array platform to evaluate DNA damage induced by enhanced X-ray radiation on gold nanofilm patches (GNFPs). Cancer cells were patterned on GNFPs of different diameters and thicknesses, where each cell was attached on one GNFP. The end-point DNA damage induced by X-ray was examined in situ at the single-cell level using a halo assay. The preliminary data demonstrated that the enhancement of DNA damage was significantly related to the area and thickness of the GNFP. This platform may be hopefully used to establish the mathematical relationships among DNA damage, X-ray dosage, and thickness and area of the GNFP, and further contribute to radiation dosage screening for personalized radiotherapy.
Keyphrases
- dna damage
- single cell
- high throughput
- rna seq
- oxidative stress
- high resolution
- dna repair
- radiation induced
- gold nanoparticles
- dual energy
- early stage
- locally advanced
- radiation therapy
- optical coherence tomography
- minimally invasive
- magnetic resonance imaging
- computed tomography
- palliative care
- electron microscopy
- cell therapy
- machine learning
- electronic health record
- combination therapy
- big data