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Diverse roles of RAD18 and Y-family DNA polymerases in tumorigenesis

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61988987%3A17310%2F18%3AA1901X15" target="_blank" >RIV/61988987:17310/18:A1901X15 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1080/15384101.2018.1456296" target="_blank" >http://dx.doi.org/10.1080/15384101.2018.1456296</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1080/15384101.2018.1456296" target="_blank" >10.1080/15384101.2018.1456296</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Diverse roles of RAD18 and Y-family DNA polymerases in tumorigenesis

  • Original language description

    Mutagenesis is a hallmark and enabling characteristic of cancer cells. The E3 ubiquitin ligase RAD18 and its downstream effectors, the Y-family' Trans-Lesion Synthesis (TLS) DNA polymerases, confer DNA damage tolerance at the expense of DNA replication fidelity. Thus, RAD18 and TLS polymerases are attractive candidate mediators of mutagenesis and carcinogenesis. The skin cancer-propensity disorder xeroderma pigmentosum-variant (XPV) is caused by defects in the Y-family DNA polymerase Pol eta (Pol). However it is unknown whether TLS dysfunction contributes more generally to other human cancers. Recent analyses of cancer genomes suggest that TLS polymerases generate many of the mutational signatures present in diverse cancers. Moreover biochemical studies suggest that the TLS pathway is often reprogrammed in cancer cells and that TLS facilitates tolerance of oncogene-induced DNA damage. Here we review recent evidence supporting widespread participation of RAD18 and the Y-family DNA polymerases in the different phases of multi-step carcinogenesis.

  • 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

    10601 - Cell biology

Result continuities

  • Project

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2018

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    CELL CYCLE

  • ISSN

    1538-4101

  • e-ISSN

  • Volume of the periodical

    17

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    833-843

  • UT code for WoS article

    000438399100004

  • EID of the result in the Scopus database