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DNA interaction with platinum-based cytostatics revealed by DNA sequencing

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62156489%3A43210%2F17%3A43912469" target="_blank" >RIV/62156489:43210/17:43912469 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14310/17:00100210 RIV/00216208:11130/17:10369484 RIV/00216208:11310/17:10369484 RIV/00216305:26620/17:PU125955 RIV/00064203:_____/17:10369484

  • Result on the web

    <a href="https://doi.org/10.1016/j.ab.2017.09.018" target="_blank" >https://doi.org/10.1016/j.ab.2017.09.018</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.ab.2017.09.018" target="_blank" >10.1016/j.ab.2017.09.018</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    DNA interaction with platinum-based cytostatics revealed by DNA sequencing

  • Original language description

    The main mechanism of action of platinum-based cytostatic drugs - cisplatin, oxaliplatin and carboplatin - is the formation of DNA cross-links, which restricts the transcription due to the disability of DNA to enter the active site of the polymerase. The polymerase chain reaction (PCR) was employed as a simplified model of the amplification process in the cell nucleus. PCR with fluorescently labelled dideoxynucleotides commonly employed for DNA sequencing was used to monitor the effect of platinum-based cytostatics on DNA in terms of decrease in labeling efficiency dependent on a presence of the DNA-drug cross-link. It was found that significantly different amounts of the drugs - cisplatin (0.21 μg/mL), oxaliplatin (5.23 μg/mL), and carboplatin (71.11 μg/mL) - were required to cause the same quenching effect (50%) on the fluorescent labelling of 50 μg/mL of DNA. Moreover, it was found that even though the amounts of the drugs was applied to the reaction mixture differing by several orders of magnitude, the amount of incorporated platinum, quantified by inductively coupled plasma mass spectrometry, was in all cases at the level of tenths of μg per 5 μg of DNA.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Analytical Biochemistry

  • ISSN

    0003-2697

  • e-ISSN

  • Volume of the periodical

    539

  • Issue of the periodical within the volume

    15 December

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    7

  • Pages from-to

    22-28

  • UT code for WoS article

    000417117000004

  • EID of the result in the Scopus database

    2-s2.0-85030719997