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Colorectal cancer specific cytochrome P450 2W1 (CYP2W1): intracellular localization, glycosylation, and catalytic activity

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00179906%3A_____%2F10%3A10080527" target="_blank" >RIV/00179906:_____/10:10080527 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Colorectal cancer specific cytochrome P450 2W1 (CYP2W1): intracellular localization, glycosylation, and catalytic activity

  • Original language description

    Cytochrome P450 2W1 (CYP2W1) is expressed at high levels in colorectal cancer cells. We have shown previously that a higher tumor expression is associated with less survival. In this study, we characterize post-translational modification, inverted endoplasmic reticulum (ER) topology, and catalytic activity of CYP2W1. Immunofluorescence microscopy and cell surface biotinylation experiments revealed approx. 8% of the CYP2W1 on the cell surface. Despite the reverse orientation of CYP2W1 in the ER membrane,apparently making interactions with NADPH-cytochrome P450 reductase impossible, CYP2W1 in HEK293 cells was active in the metabolism of indoline substrates and in activation of aflatoxin B1 into cytotoxic products. The study identifies for the first timea cytochrome P450 with a luminal ER orientation and still retaining catalytic activity. The results suggest a possibility of using CYP2W1 as a drug target in the treatment of colon cancer using antibodies and/or specific CYP2W1 activated

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    N - Vyzkumna aktivita podporovana z neverejnych zdroju

Others

  • Publication year

    2010

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Molecular Pharmacology

  • ISSN

    0026-895X

  • e-ISSN

  • Volume of the periodical

    78

  • Issue of the periodical within the volume

    6

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    8

  • Pages from-to

  • UT code for WoS article

    000284267200004

  • EID of the result in the Scopus database