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A Comprehensive Review on MAPK: A Promising Therapeutic Target in Cancer

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F19%3A00078347" target="_blank" >RIV/00209805:_____/19:00078347 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14740/19:00112969

  • Result on the web

    <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827047/" target="_blank" >https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827047/</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3390/cancers11101618" target="_blank" >10.3390/cancers11101618</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A Comprehensive Review on MAPK: A Promising Therapeutic Target in Cancer

  • Original language description

    The mitogen-activated protein kinase (MAPK) pathway is an important bridge in the switch from extracellular signals to intracellular responses. Alterations of signaling cascades are found in various diseases, including cancer, as a result of genetic and epigenetic changes. Numerous studies focused on both the homeostatic and the pathologic conduct of MAPK signaling; however, there is still much to be deciphered in terms of regulation and action models in both preclinical and clinical research. MAPK has implications in the response to cancer therapy, particularly the activation of the compensatory pathways in response to experimental MAPK inhibition. The present paper discusses new insights into MAPK as a complex cell signaling pathway with roles in the sustenance of cellular normal conduit, response to cancer therapy, and activation of compensatory pathways. Unfortunately, most MAPK inhibitors trigger resistance due to the activation of compensatory feed-back loops in tumor cells and tumor microenvironment components. Therefore, novel combinatorial therapies have to be implemented for cancer management in order to restrict the possibility of alternative pathway activation, as a perspective for developing novel therapies based on integration in translational studies.

  • 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

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

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

    Cancers (Basel)

  • ISSN

    2072-6694

  • e-ISSN

  • Volume of the periodical

    11

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    25

  • Pages from-to

    1618

  • UT code for WoS article

    000498826000215

  • EID of the result in the Scopus database

    2-s2.0-85074947906