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Quantitative proteomic profiling of pleiomorphic human sarcoma identifies CLIC1 as a dominant pro-oncogenic receptor expressed in diverse sarcoma types

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F14%3A%230000514" target="_blank" >RIV/00209805:_____/14:#0000514 - isvavai.cz</a>

  • Result on the web

    <a href="http://pubs.acs.org/doi/abs/10.1021/pr4010713" target="_blank" >http://pubs.acs.org/doi/abs/10.1021/pr4010713</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/pr4010713" target="_blank" >10.1021/pr4010713</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Quantitative proteomic profiling of pleiomorphic human sarcoma identifies CLIC1 as a dominant pro-oncogenic receptor expressed in diverse sarcoma types

  • Original language description

    Sarcomas are rare forms of cancer with a high unmet clinical need that develop in connective tissue, such as muscle, bone, nerves, cartilage, and fat. The outcome for patients is poor, with surgery and postoperative radiotherapy the standard treatment for patients. A better understanding of the molecular pathology of sarcoma may allow for the development of novel therapeutics. There are dozens of sarcoma subtypes where there is a need for targetted therapeutics, with the most commonly studied includingEwing?s sarcoma and osteosarcoma. Here we initiate a proteomics-based target-discovery program to define ?dominant? pro-oncogenic signaling targets in the most common sarcoma in adults: high-grade pleiomorphic soft tissue sarcoma. We have carried out a proteome screen using tandem mass tag isobaric labeling on three high-grade undifferentiated pleomorphic sarcoma biopsies from different tissue sites. We identified the commonly dysregulated proteins within the three sarcomas and further v

  • 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

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2014

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of proteome research

  • ISSN

    1535-3893

  • e-ISSN

  • Volume of the periodical

    13

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    17

  • Pages from-to

    2543-2559

  • UT code for WoS article

    000335490600027

  • EID of the result in the Scopus database