All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

IGF2 is an actionable target that identifies a distinct subpopulation of colorectal cancer patients with marginal response to anti-EGFR therapies

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F15%3A00082980" target="_blank" >RIV/00216224:14110/15:00082980 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1126/scitranslmed.3010445" target="_blank" >http://dx.doi.org/10.1126/scitranslmed.3010445</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1126/scitranslmed.3010445" target="_blank" >10.1126/scitranslmed.3010445</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    IGF2 is an actionable target that identifies a distinct subpopulation of colorectal cancer patients with marginal response to anti-EGFR therapies

  • Original language description

    Among patients with colorectal cancer who benefit from therapy targeted to the epidermal growth factor receptor (EGFR), stable disease (SD) occurs more frequently than massive regressions. Exploring the mechanisms of this incomplete sensitivity to devisemore efficacious treatments will likely improve patients' outcomes. We tested therapies tailored around hypothesis-generating molecular features in patient-derived xenografts ("xenopatients"), which originated from 125 independent samples that did not harbor established resistance-conferring mutations. Samples from xenopatients that responded to cetuximab, an anti-EGFR agent, with disease stabilization displayed high levels of EGFR family ligands and receptors, indicating high EGFR pathway activity. Five of 21 SD models (23.8%) characterized by particularly high expression of EGFR and EGFR family members regressed after intensified EGFR blockade by cetuximab and a small-molecule inhibitor.

  • 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

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2015

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    SCIENCE TRANSLATIONAL MEDICINE

  • ISSN

    1946-6234

  • e-ISSN

  • Volume of the periodical

    7

  • Issue of the periodical within the volume

    272

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    13

  • Pages from-to

    "272ra12"

  • UT code for WoS article

    000349422700005

  • EID of the result in the Scopus database