Extrachromosomal DNA (ecDNA) are circular DNA structures associated with cancer and drug resistance. One specific type, double minute (DM) chromosomes, has been studied since the 1960s using imaging techniques like cytogenetics and fluorescence microscopy. Specialized techniques such as atomic force microscopy (AFM) and scanning electron microscopy (SEM) offer micro to nano-scale visualization, but current sample preparation methods may not optimally preserve ecDNA structure. Our study introduces a systematic protocol using SEM for high-resolution ecDNA visualization. We have optimized the end-to-end procedure, providing a standardized approach to explore the circular architecture of ecDNA and address the urgent need for better understanding in cancer research.
Keyphrases
- electron microscopy
- single molecule
- atomic force microscopy
- high resolution
- high speed
- papillary thyroid
- circulating tumor
- cell free
- randomized controlled trial
- squamous cell
- molecularly imprinted
- squamous cell carcinoma
- lymph node metastasis
- palliative care
- young adults
- circulating tumor cells
- childhood cancer
- metabolic syndrome
- minimally invasive