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Tubulins as therapeutic targets in cancer: from bench to bedside

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F12%3A00387835" target="_blank" >RIV/68378050:_____/12:00387835 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.2174/138161212800626193" target="_blank" >http://dx.doi.org/10.2174/138161212800626193</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2174/138161212800626193" target="_blank" >10.2174/138161212800626193</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Tubulins as therapeutic targets in cancer: from bench to bedside

  • Original language description

    Tubulin is the target of some of the most widely used and time-honored anticancer tubulin-binding agents (TBAs). The clinical usefulness of many TBAs has been held back as a result of tumor cell drug-resistance. The elucidation of the three-dimensional structure of alpha beta-tubulin dimer has provided an opportunity for rational drug design aimed at generating compounds that will target tubulin in therapeutically more efficacious ways compared to presently available drugs. An issue to be addressed is which one(s) of the tubulin species, their isotypes, or their posttranslationally modified forms, should be specifically targeted in cancer chemotherapy. This review offers a critical appraisal of current knowledge on tubulins in cancer and an update on new anti-neoplastic microtubule-targeted treatment strategies. Specifically, it examines, across disciplines, cellular/molecular, biochemical, clinical/pathological, and pharmacological aspects of beta-tubulin isotypes, posttranslational m

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EB - Genetics and molecular biology

  • 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)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2012

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Current Pharmaceutical Design

  • ISSN

    1381-6128

  • e-ISSN

  • Volume of the periodical

    18

  • Issue of the periodical within the volume

    19

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    15

  • Pages from-to

    2778-2792

  • UT code for WoS article

    000306546900010

  • EID of the result in the Scopus database