Detection of Sialic Acid to Differentiate Cervical Cancer Cell Lines Using a Sambucus nigra Lectin Biosensor.
Ricardo Zamudio CañasMaría Eugenia Jaramillo FloresVerónica Vallejo RuizRaul Jacobo Delgado-MacuilValentín López GayouPublished in: Biosensors (2024)
Pap smear screening is a widespread technique used to detect premalignant lesions of cervical cancer (CC); however, it lacks sensitivity, leading to identifying biomarkers that improve early diagnosis sensitivity. A characteristic of cancer is the aberrant sialylation that involves the abnormal expression of α2,6 sialic acid, a specific carbohydrate linked to glycoproteins and glycolipids on the cell surface, which has been reported in premalignant CC lesions. This work aimed to develop a method to differentiate CC cell lines and primary fibroblasts using a novel lectin-based biosensor to detect α2,6 sialic acid based on attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and chemometric. The biosensor was developed by conjugating gold nanoparticles (AuNPs) with 5 µg of Sambucus nigra (SNA) lectin as the biorecognition element. Sialic acid detection was associated with the signal amplification in the 1500-1350 cm -1 region observed by the surface-enhanced infrared absorption spectroscopy (SEIRA) effect from ATR-FTIR results. This region was further analyzed for the clustering of samples by applying principal component analysis (PCA) and confidence ellipses at a 95% interval. This work demonstrates the feasibility of employing SNA biosensors to discriminate between tumoral and non-tumoral cells, that have the potential for the early detection of premalignant lesions of CC.
Keyphrases
- gold nanoparticles
- label free
- cell surface
- sensitive detection
- quantum dots
- induced apoptosis
- squamous cell carcinoma
- single cell
- mycobacterium tuberculosis
- pulmonary tuberculosis
- real time pcr
- dna damage response
- reduced graphene oxide
- papillary thyroid
- extracellular matrix
- binding protein
- risk assessment
- rna seq
- cell proliferation
- young adults
- long non coding rna
- childhood cancer