Microfluidic-SERS Technologies for CTC: A Perspective on Clinical Translation.
Amin Hassanzadeh-BarforoushiAnastasiia TukovaAudrey NadaliniDavid W InglisSimon Chang-Hao TsaoYuling WangPublished in: ACS applied materials & interfaces (2024)
Enumeration and phenotypic profiling of circulating tumor cells (CTCs) provide critical information for clinical diagnosis and treatment monitoring in cancer. To achieve this goal, an integrated system is needed to efficiently isolate CTCs from patient samples and sensitively evaluate their phenotypes. Such integration would comprise a high-throughput single-cell processing unit for the isolation and manipulation of CTCs and a sensitive and multiplexed quantitation unit to detect clinically relevant signals from these cells. Surface-enhanced Raman scattering (SERS) has been used as an analytical method for molecular profiling and in vitro cancer diagnosis. More recently, its multiplexing capability and power to create distinct molecular signatures against their targets have garnered attention. Here, we share our insights into the combined power of microfluidics and SERS in realizing CTC isolation, enumeration, and detection from a clinical translation perspective. We highlight the key operational factors in CTC microfluidic processing and SERS detection from patient samples. We further discuss microfluidic-SERS integration and its clinical utility as a paradigm shift in clinical CTC-based cancer diagnosis and prognostication. Finally, we summarize the challenges and attempt to look forward to what lies ahead of us in potentially translating the technique into real clinical applications.
Keyphrases
- circulating tumor cells
- single cell
- gold nanoparticles
- circulating tumor
- high throughput
- sensitive detection
- label free
- papillary thyroid
- rna seq
- squamous cell
- case report
- loop mediated isothermal amplification
- ms ms
- lymph node metastasis
- gene expression
- induced apoptosis
- mass spectrometry
- signaling pathway
- working memory
- oxidative stress
- quantum dots
- high resolution
- endoplasmic reticulum stress
- single molecule
- solid phase extraction