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Colon Cancer and Perturbations of the Sphingolipid Metabolism

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00027162%3A_____%2F19%3AN0000177" target="_blank" >RIV/00027162:_____/19:N0000177 - isvavai.cz</a>

  • Alternative codes found

    RIV/68081707:_____/19:00520477

  • Result on the web

    <a href="https://www.mdpi.com/1422-0067/20/23/6051" target="_blank" >https://www.mdpi.com/1422-0067/20/23/6051</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3390/ijms20236051" target="_blank" >10.3390/ijms20236051</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Colon Cancer and Perturbations of the Sphingolipid Metabolism

  • Original language description

    Colon Cancer and Perturbations of theSphingolipid Metabolism - The development and progression of colorectal cancer (CRC), a major cause of cancer-relateddeath in the western world, is accompanied with alterations of sphingolipid (SL) composition in colontumors. A number of enzymes involved in the SL metabolism have been found to be deregulatedin human colon tumors, in experimental rodent studies, and in human colon cancer cellsin vitro.Therefore, the enzymatic pathways that modulate SL levels have received a significant attention, due to their possible contribution to CRC development, or as potential therapeutic targets. Many of theseenzymes are associated with an increased sphingosine-1-phosphate/ceramide ratio, which is in turnlinked with increased colon cancer cell survival, proliferation and cancer progression. Nevertheless,more attention should also be paid to the more complex SLs, including specific glycosphingolipids,such as lactosylceramides, which can be also deregulated during CRC development. In this review,we focus on the potential roles of individual SLs/SL metabolism enzymes in colon cancer, as wellas on the pros and cons of employing the current in vitro models of colon cancer cells for lipidomicstudies investigating the SL metabolism in CRC.

  • 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

    30107 - Medicinal chemistry

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

    2019

  • 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 Molecular Sciences

  • ISSN

    1422-0067

  • e-ISSN

  • Volume of the periodical

    20

  • Issue of the periodical within the volume

    23

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    14

  • Pages from-to

    6051

  • UT code for WoS article

    000504428300233

  • EID of the result in the Scopus database