Quantitative Evaluation of Cisplatin Uptake in Sensitive and Resistant Individual Cells by Single-Cell ICP-MS (SC-ICP-MS)

被引:116
作者
Corte Rodriguez, M. [1 ]
Alvarez-Fernandez Garcia, R. [1 ]
Blanco, E. [1 ]
Bettmer, J. [1 ]
Montes-Bayon, M. [1 ]
机构
[1] Univ Oviedo, Fac Chem, Dept Phys & Analyt Chem, C Julian Claveria 8, E-33006 Oviedo, Spain
关键词
INDUCTIVELY-COUPLED PLASMA; ANTICANCER DRUG CISPLATIN; FIELD MASS-SPECTROMETER; DNA ADDUCTS; NANOPARTICLES; YEAST; MODE; GOLD;
D O I
10.1021/acs.analchem.7b02746
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
One of the main limitations to the Pt-therapy in cancer is the development of associated drug resistance that can be associated with a significant reduction of the intracellular platinum concentration. Thus, intracellular Pt concentration could be considered as a biomarker of cisplatin resistance. In this work, an alternative method to address intracellular Pt concentration in individual cells is explored to permit the evaluation of different cell models and alternative therapies in a relatively fast way. For this aim, total Pt analysis in single cells has been implemented using a total consumption nebulizer coupled to inductively coupled plasma mass spectrometric detection (ICP-MS). The efficiency of the proposed device has been evaluated in combination with flow cytometry and turned out to be around 25% (cells entering the ICP-MS from the cells in suspension). Quantitative uptake studies of a nontoxic Tb-containing compound by individual cells were conducted and the results compared to those obtained by bulk analysis of the same cells. Both sets of data were statistically comparable. Thus, final application of the developed methodology to the comparative uptake of Pt-species in cisplatin resistant and sensitive cell lines (A2780cis and A2780) was conducted. The results obtained revealed the potential of this analytical strategy to differentiate between different cell lines of different sensitivity to the drug which might be of high medical interest.
引用
收藏
页码:11491 / 11497
页数:7
相关论文
共 33 条
  • [1] Amable L., 2017, APPL NOTE 013176 01
  • [2] Cisplatin resistance and opportunities for precision medicine
    Amable, Lauren
    [J]. PHARMACOLOGICAL RESEARCH, 2016, 106 : 27 - 36
  • [3] Recognition and processing of cisplatin- and oxaliplatin-DNA adducts
    Chaney, SG
    Campbell, SL
    Bassett, E
    Wu, YB
    [J]. CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2005, 53 (01) : 3 - 11
  • [4] Single-cell measurement of the uptake, intratumoral distribution and cell cycle effects of cisplatin using mass cytometry
    Chang, Qing
    Ornatsky, Olga I.
    Koch, Cameron J.
    Chaudary, Naz
    Marie-Egyptienne, Delphine T.
    Hill, Richard P.
    Tanner, Scott D.
    Hedley, David W.
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2015, 136 (05) : 1202 - 1209
  • [5] Quantitative evaluation of cellular uptake, DNA incorporation and adduct formation in cisplatin sensitive and resistant cell lines: Comparison of different Pt-containing drugs
    Corte-Rodriguez, M.
    Espina, M.
    Sierra, L. M.
    Blanco, E.
    Ames, T.
    Montes-Bayon, M.
    Sanz-Medel, A.
    [J]. BIOCHEMICAL PHARMACOLOGY, 2015, 98 (01) : 69 - 77
  • [6] De Stasio C, 2001, CANCER RES, V61, P4272
  • [7] Gold colloid analysis by inductively coupled plasma-mass spectrometry in a single particle mode
    Degueldre, C
    Favarger, PY
    Wold, S
    [J]. ANALYTICA CHIMICA ACTA, 2006, 555 (02) : 263 - 268
  • [8] Quantitative Imaging of Gold and Silver Nanoparticles in Single Eukaryotic Cells by Laser Ablation ICP-MS
    Drescher, Daniela
    Giesen, Charlotte
    Traub, Heike
    Panne, Ulrich
    Kneipp, Janina
    Jakubowski, Norbert
    [J]. ANALYTICAL CHEMISTRY, 2012, 84 (22) : 9684 - 9688
  • [10] Molecular mechanisms of cisplatin resistance
    Galluzzi, L.
    Senovilla, L.
    Vitale, I.
    Michels, J.
    Martins, I.
    Kepp, O.
    Castedo, M.
    Kroemer, G.
    [J]. ONCOGENE, 2012, 31 (15) : 1869 - 1883