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Discrimination between drug-resistant and non-resistant human melanoma cell lines by FTIR spectroscopy
- Source :
- The Analyst. 134:294-300
- Publication Year :
- 2009
- Publisher :
- Royal Society of Chemistry (RSC), 2009.
-
Abstract
- We investigated the ability of FTIR-microscopy to define spectral changes between drug-sensitive and drug-resistant human melanoma cells. As a model system, a resistant melanoma cell line (GAC) was selected with cisplatin from parental (GA) cells. Using Fourier transform infrared spectroscopy (FTIR) we investigated the ability to differentiate between the resistant variant derived from the sensitive parental cell line, in the absence of cisplatin. We determined and validated spectral parameters (biomarkers) that differentiated between the two cell lines. By applying the principal component analysis (PCA) model, we reduced the original data size to six principal components. We detected a significant and consistent increase in the cell's DNA/RNA ratio as well as an increase in the lipid/protein ratio in the resistant cells. These results strongly support the potential of developing FTIR microspectroscopy as a simple, reagent-free method for the identification of drug-resistant cells. Rapid detection of tumors resistant to a particular drug, should contribute to the ability of the physician to choose an effective treatment protocol.
- Subjects :
- Skin Neoplasms
Cell
Infrared spectroscopy
Antineoplastic Agents
Biochemistry
Fourier transform spectroscopy
Analytical Chemistry
chemistry.chemical_compound
Cell Line, Tumor
Spectroscopy, Fourier Transform Infrared
Electrochemistry
medicine
Humans
Environmental Chemistry
Fourier transform infrared spectroscopy
Melanoma
Spectroscopy
Cisplatin
Principal Component Analysis
RNA
Molecular biology
medicine.anatomical_structure
chemistry
Drug Resistance, Neoplasm
Cell culture
Algorithms
DNA
medicine.drug
Subjects
Details
- ISSN :
- 13645528 and 00032654
- Volume :
- 134
- Database :
- OpenAIRE
- Journal :
- The Analyst
- Accession number :
- edsair.doi.dedup.....cd1b29481fdcbd3e3bf5a5596607c9f5
- Full Text :
- https://doi.org/10.1039/b805223a