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Inositol hexaphosphate limits the migration and the invasiveness of colorectal carcinoma cells in vitro

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11150%2F18%3A10383421" target="_blank" >RIV/00216208:11150/18:10383421 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11160/18:10383421

  • Result on the web

    <a href="http://www.spandidos-publications.com/10.3892/ijo.2018.4488" target="_blank" >http://www.spandidos-publications.com/10.3892/ijo.2018.4488</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3892/ijo.2018.4488" target="_blank" >10.3892/ijo.2018.4488</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Inositol hexaphosphate limits the migration and the invasiveness of colorectal carcinoma cells in vitro

  • Original language description

    Inositol hexaphosphate (IP6), also known as phytic acid, has been shown to exhibit anticancer effects in a number of preclinical tumor models. IP6 decreases proliferation by arresting cells in the GO/G1 phase, inhibits iron-mediated oxidative reactions, enhances differentiation and stimulates apoptosis. The present study attempted to characterize the effect of IP6 on the migration and adhesion of colon cancer SW620 cells. IP6 was assessed at concentrations of 0.2 and 1 mM during 12, 24 and 48 h of exposure. Migration ability was measured with the real-time xCELLigence Real-Time Cell Analyzer Dual Purpose system. The expression of mRNA and proteins involved in migration and cancer progression [epithelial cell adhesion molecule, intercellular adhesion molecule-1, beta-catenin, N-cadherin, E-cadherin, matrix metalloproteinase MMP-2 and MMP-9] was determined by reverse transcription-quantitative polymerase chain reaction and western blot analysis. The changes in the expression and subcellular localization of E-cadherin were determined by indirect immunofluorescence. IP6 induced a decrease in the migration ability of the tested SW620 cell line. IP6-treated cells also showed decreased expression of N-cadherin, increased levels of E-cadherin and decreased expression of MMP-2 and MMP-9. These results indicated that IP6 has potential to modulate the migration ability and expression of markers associated with invasion in SW620 cells; however, further analysis is necessary to obtain a detailed understanding of the mechanism of action.

  • 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

    10600 - Biological sciences

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

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

    International Journal of Oncology

  • ISSN

    1019-6439

  • e-ISSN

  • Volume of the periodical

    53

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    GR - GREECE

  • Number of pages

    8

  • Pages from-to

    1625-1632

  • UT code for WoS article

    000442971100017

  • EID of the result in the Scopus database

    2-s2.0-85052284885