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Expression of human BRCA1 Delta 17-19 alternative splicing variant with a truncated BRCT domain in MCF-7 cells results in impaired assembly of DNA repair complexes and aberrant DNA damage response

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F13%3A10188875" target="_blank" >RIV/00216208:11110/13:10188875 - isvavai.cz</a>

  • Alternative codes found

    RIV/68081707:_____/13:00394847 RIV/68378050:_____/13:00394847 RIV/00216208:11120/13:43907401 RIV/61989592:15110/13:33143747

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.cellsig.2013.02.008" target="_blank" >http://dx.doi.org/10.1016/j.cellsig.2013.02.008</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.cellsig.2013.02.008" target="_blank" >10.1016/j.cellsig.2013.02.008</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Expression of human BRCA1 Delta 17-19 alternative splicing variant with a truncated BRCT domain in MCF-7 cells results in impaired assembly of DNA repair complexes and aberrant DNA damage response

  • Original language description

    Alternative pre-mRNA splicing is a fundamental post-transcriptional regulatory mechanism. Cancer-specific misregulation of the splicing process may lead to formation of irregular alternative splicing variants (ASVs) with a potentially negative impact oncellular homeostasis. Alternative splicing of BRCA1 pre-mRNA can give rise to BRCA1 protein isoforms that possess dramatically altered biological activities compared with full-length wild-type BRCAl. During the screening of high-risk breast cancer (BC) families we ascertained numerous BRCA1 ASVs, however, their clinical significance for BC development is largely unknown. In this study, we examined the influence of the BRCA1 Delta 17-19 ASV, which lacks a portion of the BRCT domain, on DNA repair capacity using human MCF-7 BC cell clones with stably modified BRCA1 expression. Our results show that overexpression of BRCA1 Delta 17-19 impairs homologous recombination repair (sensitizes cells to mitomycin C), delays repair of ionizing radia

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

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

  • Continuities

    S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2013

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Cellular Signalling

  • ISSN

    0898-6568

  • e-ISSN

  • Volume of the periodical

    25

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    8

  • Pages from-to

    1186-1193

  • UT code for WoS article

    000318377300016

  • EID of the result in the Scopus database