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Senescence Induced by DNA Demethylating Drugs to Treat Solid Tumors

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F18%3A00069116" target="_blank" >RIV/00159816:_____/18:00069116 - isvavai.cz</a>

  • Výsledek na webu

    <a href="http://dx.doi.org/10.1007/978-3-319-64597-1_166-1" target="_blank" >http://dx.doi.org/10.1007/978-3-319-64597-1_166-1</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/978-3-319-64597-1_166-1" target="_blank" >10.1007/978-3-319-64597-1_166-1</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Senescence Induced by DNA Demethylating Drugs to Treat Solid Tumors

  • Popis výsledku v původním jazyce

    DNA methylation is a process by which methyl groups are added to DNA, modifying its function. When located in a gene promoter, DNA methylation typically acts to repress gene transcription. DNA methylation is aberrant in all forms of cancer, but it is not fully understood how this occurs and what is its role in tumorigenesis. Aberrant DNA methylation in cancer can be generated following cell transformation or generated in a programmed manner in a subpopulation of tissue cells during normal aging and cell senescence predisposing them for tumorigenesis. Regardless, DNA methylation contributes to the tumor state by inhibiting the plasticity of cell differentiation DNA methylation. DNA demethylating agents, such as decitabine, exert their anticancer activity by triggering a drug-induced cell senescence program that induces cancer cells to exit cell cycle and stop proliferating, which is considered per se an important tumor suppressive mechanism. Moreover, specific senescence-associated DNA methylation changes are observed in normal and cancer cells. In this chapter we will describe advances in our knowledge about (i) the development of novel generation DNA demethylating drugs and (ii) the molecular mediators, prognostic indicators, and tailoring tools for DNA demethylating drug-induced senescence in cancer cells. We focus on solid tumors, in particular on gastrointestinal tumors, and we describe the current evidence that epigenetic hypomethylation therapies possess significant immunomodulatory effects by controlling cell senescence. The immunomodulatory activities of DNA demethylating drugs might lead to improved immune recognition of cancer/senescent cells and on novel immunotherapies through combinatorial epigenetic immunotherapy approaches.

  • Název v anglickém jazyce

    Senescence Induced by DNA Demethylating Drugs to Treat Solid Tumors

  • Popis výsledku anglicky

    DNA methylation is a process by which methyl groups are added to DNA, modifying its function. When located in a gene promoter, DNA methylation typically acts to repress gene transcription. DNA methylation is aberrant in all forms of cancer, but it is not fully understood how this occurs and what is its role in tumorigenesis. Aberrant DNA methylation in cancer can be generated following cell transformation or generated in a programmed manner in a subpopulation of tissue cells during normal aging and cell senescence predisposing them for tumorigenesis. Regardless, DNA methylation contributes to the tumor state by inhibiting the plasticity of cell differentiation DNA methylation. DNA demethylating agents, such as decitabine, exert their anticancer activity by triggering a drug-induced cell senescence program that induces cancer cells to exit cell cycle and stop proliferating, which is considered per se an important tumor suppressive mechanism. Moreover, specific senescence-associated DNA methylation changes are observed in normal and cancer cells. In this chapter we will describe advances in our knowledge about (i) the development of novel generation DNA demethylating drugs and (ii) the molecular mediators, prognostic indicators, and tailoring tools for DNA demethylating drug-induced senescence in cancer cells. We focus on solid tumors, in particular on gastrointestinal tumors, and we describe the current evidence that epigenetic hypomethylation therapies possess significant immunomodulatory effects by controlling cell senescence. The immunomodulatory activities of DNA demethylating drugs might lead to improved immune recognition of cancer/senescent cells and on novel immunotherapies through combinatorial epigenetic immunotherapy approaches.

Klasifikace

  • Druh

    C - Kapitola v odborné knize

  • CEP obor

  • OECD FORD obor

    10608 - Biochemistry and molecular biology

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/EF15_003%2F0000492" target="_blank" >EF15_003/0000492: Mapování molekulární podstaty procesů stárnutí pro vývoj nových léčebných metod</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Ostatní

  • Rok uplatnění

    2018

  • Kód důvěrnosti údajů

    C - Předmět řešení projektu podléhá obchodnímu tajemství (§ 504 Občanského zákoníku), ale název projektu, cíle projektu a u ukončeného nebo zastaveného projektu zhodnocení výsledku řešení projektu (údaje P03, P04, P15, P19, P29, PN8) dodané do CEP, jsou upraveny tak, aby byly zveřejnitelné.

Údaje specifické pro druh výsledku

  • Název knihy nebo sborníku

    Handbook of Immunosenescence

  • ISBN

    978-3-319-64597-1

  • Počet stran výsledku

    30

  • Strana od-do

    1-30

  • Počet stran knihy

    2970

  • Název nakladatele

    Springer

  • Místo vydání

    Cham

  • Kód UT WoS kapitoly