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Intercellular crosstalk in human malignant melanoma

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F17%3A00477963" target="_blank" >RIV/68378050:_____/17:00477963 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11110/17:10362296 RIV/00064165:_____/17:10362296

  • Result on the web

    <a href="http://dx.doi.org/10.1007/s00709-016-1038-z" target="_blank" >http://dx.doi.org/10.1007/s00709-016-1038-z</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00709-016-1038-z" target="_blank" >10.1007/s00709-016-1038-z</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Intercellular crosstalk in human malignant melanoma

  • Original language description

    Incidence of malignant melanoma is increasing globally. While the initial stages of tumors can be easily treated by a simple surgery, the therapy of advanced stages is rather limited. Melanoma cells spread rapidly through the body of a patient to form multiple metastases. Consequently, the survival rate is poor. Therefore, emphasis in melanoma research is given on early diagnosis and development of novel and more potent therapeutic options. The malignant melanoma is arising from melanocytes, cells protecting mitotically active keratinocytes against damage caused by UV light irradiation. The melanocytes originate in the neural crest and consequently migrate to the epidermis. The relationship between the melanoma cells, the melanocytes, and neural crest stem cells manifests when the melanoma cells are implanted to an early embryo: they use similar migratory routes as the normal neural crest cells. Moreover, malignant potential of these melanoma cells is overdriven in this experimental model, probably due to microenvironmental reprogramming. This observation demonstrates the crucial role of the microenvironment in melanoma biology. Indeed, malignant tumors in general represent complex ecosystems, where multiple cell types influence the growth of genetically mutated cancer cells. This concept is directly applicable to the malignant melanoma. Our review article focuses on possible strategies to modify the intercellular crosstalk in melanoma that can be employed for therapeutic purposes.

  • 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

    10601 - Cell biology

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

    2017

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Protoplasma

  • ISSN

    0033-183X

  • e-ISSN

  • Volume of the periodical

    254

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    AT - AUSTRIA

  • Number of pages

    8

  • Pages from-to

    1143-1150

  • UT code for WoS article

    000399037400002

  • EID of the result in the Scopus database