4.6 Article

CARS based label-free assay for assessment of drugs by monitoring lipid droplets in tumour cells

期刊

JOURNAL OF BIOPHOTONICS
卷 7, 期 11-12, 页码 906-913

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/jbio.201300110

关键词

Coherent anti-Stokes Raman scattering; CARS; label-free imaging; lipid droplets; cell stress; apoptosis; drug efficiency; drug screening

资金

  1. EPSRC [EP/H028757/1, EP/H028757/2]
  2. Royal Society Research Grant award [RG2011R2]
  3. Cambridge Cancer Centre (CCC) pump-priming award
  4. EPSRC [EP/H028757/1, EP/H028757/2]
  5. Royal Society Research Grant award [RG2011R2]
  6. Cambridge Cancer Centre (CCC) pump-priming award
  7. EPSRC [EP/G03088X/1] Funding Source: UKRI
  8. EPSRC [EP/H028757/2, EP/H028757/1] Funding Source: UKRI
  9. Cancer Research UK [16465, 17242, 22310] Funding Source: researchfish
  10. Engineering and Physical Sciences Research Council [EP/H028757/2, EP/H028757/1, EP/G03088X/1] Funding Source: researchfish

向作者/读者索取更多资源

Coherent anti-Stokes Raman scattering (CARS) is becoming an established tool for label-free multi-photon imaging based on molecule specific vibrations in the sample. The technique has proven to be particularly useful for imaging lipids, which are abundant in cells and tissues, including cytoplasmic lipid droplets (LD), which are recognized as dynamic organelles involved in many cellular functions. The increase in the number of lipid droplets in cells undergoing cell proliferation is a common feature in many neoplastic processes [1] and an increase in LD number also appears to be an early marker of drug-induced cell stress and subsequent apoptosis [3]. In this paper, a CARS-based label-free method is presented to monitor the increase in LD content in HCT116 colon tumour cells treated with the chemotherapeutic drugs Etoposide, Camptothecin and the protein kinase inhibitor Staurosporine. Using CARS, LDs can easily be distinguished from other cell components without the application of fluorescent dyes and provides a label-free non-invasive drug screening assay that could be used not only with cells and tissues ex vivo but potentially also in vivo. ((c) 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)

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