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Traffic lights for retinoids in oncology: molecular markers of retinoid resistance and sensitivity and their use in the management of cancer differentiation therapy

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F18%3A00069100" target="_blank" >RIV/00159816:_____/18:00069100 - isvavai.cz</a>

  • Alternative codes found

    RIV/65269705:_____/18:00069100 RIV/00216224:14310/18:00106966

  • Result on the web

    <a href="https://bmccancer.biomedcentral.com/articles/10.1186/s12885-018-4966-5" target="_blank" >https://bmccancer.biomedcentral.com/articles/10.1186/s12885-018-4966-5</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1186/s12885-018-4966-5" target="_blank" >10.1186/s12885-018-4966-5</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Traffic lights for retinoids in oncology: molecular markers of retinoid resistance and sensitivity and their use in the management of cancer differentiation therapy

  • Original language description

    For decades, retinoids and their synthetic derivatives have been well established anticancer treatments due to their ability to regulate cell growth and induce cell differentiation and apoptosis. Many studies have reported the promising role of retinoids in attaining better outcomes for adult or pediatric patients suffering from several types of cancer, especially acute myeloid leukemia and neuroblastoma. However, even this promising differentiation therapy has some limitations: retinoid toxicity and intrinsic or acquired resistance have been observed in many patients. Therefore, the identification of molecular markers that predict the therapeutic response to retinoid treatment is undoubtedly important for retinoid use in clinical practice. The purpose of this review is to summarize the current knowledge on candidate markers, including both genetic alterations and protein markers, for retinoid resistance and sensitivity in human malignancies.

  • 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

    30204 - Oncology

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

    2018

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    BMC Cancer

  • ISSN

    1471-2407

  • e-ISSN

  • Volume of the periodical

    18

  • Issue of the periodical within the volume

    NOV 1 2018

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    13

  • Pages from-to

    1059

  • UT code for WoS article

    000449121200004

  • EID of the result in the Scopus database

    2-s2.0-85055906370