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  1. Article: Two Targets, One Hit: new Anticancer Therapeutics to Prevent Tumorigenesis Without Cardiotoxicity.

    Szabó, Zoltán / Hornyák, Lilla / Miskei, Márton / Székvölgyi, Lóránt

    Frontiers in pharmacology

    2021  Volume 11, Page(s) 569955

    Abstract: A serious adverse effect of cancer therapies is cardiovascular toxicity, which significantly limits the widespread use of antineoplastic agents. The promising new field of cardio-oncology offers the identification of potent anti-cancer therapeutics that ... ...

    Abstract A serious adverse effect of cancer therapies is cardiovascular toxicity, which significantly limits the widespread use of antineoplastic agents. The promising new field of cardio-oncology offers the identification of potent anti-cancer therapeutics that effectively inhibit cancer cell proliferation without causing cardiotoxicity. Future introduction of recently identified cardio-safe compounds into clinical practice (including ERK dimerization inhibitors or BAX allosteric inhibitors) is expected to help oncologists avoid unwanted cardiological complications associated with therapeutic interventions.
    Language English
    Publishing date 2021-02-10
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2587355-6
    ISSN 1663-9812
    ISSN 1663-9812
    DOI 10.3389/fphar.2020.569955
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Histone H3 Lysine 56 Acetylation Is Required for Formation of Normal Levels of Meiotic DNA Breaks in

    Karányi, Zsolt / Hornyák, Lilla / Székvölgyi, Lóránt

    Frontiers in cell and developmental biology

    2020  Volume 7, Page(s) 364

    Abstract: Meiotic recombination is initiated by Spo11-catalyzed DNA double-strand breaks (DSBs) that are promoted by histone modifications and histone modifying enzymes. Herein we investigated the role of histone H3 lysine 56 acetylation (H3K56ac) located near the ...

    Abstract Meiotic recombination is initiated by Spo11-catalyzed DNA double-strand breaks (DSBs) that are promoted by histone modifications and histone modifying enzymes. Herein we investigated the role of histone H3 lysine 56 acetylation (H3K56ac) located near the entry/exit points of the DNA in the globular H3 domain. We generated a series of mutant cells (
    Language English
    Publishing date 2020-01-10
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2737824-X
    ISSN 2296-634X
    ISSN 2296-634X
    DOI 10.3389/fcell.2019.00364
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Longitudinal Analysis of 1α,25-dihidroxyvitamin D

    Mühl, Dorottya / Herold, Magdolna / Herold, Zoltan / Hornyák, Lilla / Szasz, Attila Marcell / Dank, Magdolna

    Cancers

    2022  Volume 14, Issue 3

    Abstract: Background: 1α,25-dihydroxycholecalciferol (1,25(OH): Methods: The serum 1,25(OH): Results: 1,25(OH): Conclusions: A measurement-based titration of vitamin ... ...

    Abstract Background: 1α,25-dihydroxycholecalciferol (1,25(OH)
    Methods: The serum 1,25(OH)
    Results: 1,25(OH)
    Conclusions: A measurement-based titration of vitamin D
    Language English
    Publishing date 2022-01-28
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers14030658
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Does Elevated Pre-Treatment Plasma PD-L1 Level Indicate an Increased Tumor Burden and Worse Prognosis in Metastatic Colorectal Cancer?

    Dank, Magdolna / Mühl, Dorottya / Herold, Magdolna / Hornyák, Lilla / Szasz, Attila Marcell / Herold, Zoltan

    Journal of clinical medicine

    2022  Volume 11, Issue 16

    Abstract: Background: Programmed death-ligand 1 (PD-L1) and programmed cell death protein 1 (PD-1) have been reported as possibly favorable prognostic factors in colorectal cancer (CRC). However, their longitudinal effect is unknown.: Methods: A pilot study ... ...

    Abstract Background: Programmed death-ligand 1 (PD-L1) and programmed cell death protein 1 (PD-1) have been reported as possibly favorable prognostic factors in colorectal cancer (CRC). However, their longitudinal effect is unknown.
    Methods: A pilot study was performed to investigate whether baseline PD-1/PD-L1 levels are associated with further laboratory changes and/or shorter survival.
    Results: A total of 506 laboratory measurements from 37 metastatic CRC patients were analyzed. The baseline plasma PD-1 and PD-L1 levels were 27.73 ± 1.20 pg/mL and 16.01 ± 1.09 pg/mL, respectively. Disease progression (
    Conclusions: Abnormal levels of laboratory parameters and intensified tumor burden can be expected if elevated baseline plasma PD-1/PD-L1 levels are found.
    Language English
    Publishing date 2022-08-17
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662592-1
    ISSN 2077-0383
    ISSN 2077-0383
    DOI 10.3390/jcm11164815
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Commentary: Nuclear dynamics of the Set1C subunit Spp1 prepares meiotic recombination sites for break formation.

    Fillér, Csaba / Hornyák, Lilla / Roszik, Jason

    Frontiers in genetics

    2018  Volume 9, Page(s) 496

    Language English
    Publishing date 2018-10-23
    Publishing country Switzerland
    Document type Journal Article ; Comment
    ZDB-ID 2606823-0
    ISSN 1664-8021
    ISSN 1664-8021
    DOI 10.3389/fgene.2018.00496
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Drugging the R-loop interactome: RNA-DNA hybrid binding proteins as targets for cancer therapy.

    Boros-Oláh, Beáta / Dobos, Nikoletta / Hornyák, Lilla / Szabó, Zoltán / Karányi, Zsolt / Halmos, Gábor / Roszik, Jason / Székvölgyi, Lóránt

    DNA repair

    2019  Volume 84, Page(s) 102642

    Abstract: Unravelling the origin of genetic alterations from point mutations to chromosomal rearrangements was greatly enhanced by the discovery of RNA-DNA hybrids (R-loops) that behave as hotspots of genomic instability in a variety of organisms. Current models ... ...

    Abstract Unravelling the origin of genetic alterations from point mutations to chromosomal rearrangements was greatly enhanced by the discovery of RNA-DNA hybrids (R-loops) that behave as hotspots of genomic instability in a variety of organisms. Current models suggest that uncontrolled R-loops are a hazard to genome integrity, therefore, identifying proteins that are involved in recognising and signalling R-loop structures are of key importance. Herein we analysed key RNA-DNA hybrid binding proteins in humans taking advantage of large-scale gene expression, survival rate, and drug-sensitivity data from cancer genomics databases. We show that expression of RNA-DNA hybrid binding proteins in various cancer types is associated with survival and may have contrasting outcomes in responding to therapeutic treatments. Based on the revealed pharmacogenomic landscape of human RNA-DNA hybrid binding proteins, we propose that R-loops and R-loop binding proteins are potentially relevant new epigenetic markers and therapeutic targets in multiple cancers.
    MeSH term(s) Antineoplastic Agents/pharmacology ; Cell Line, Tumor ; DNA-Binding Proteins/metabolism ; Genomic Instability ; Humans ; Neoplasms/genetics ; Protein Binding/drug effects ; R-Loop Structures ; RNA-Binding Proteins/metabolism
    Chemical Substances Antineoplastic Agents ; DNA-Binding Proteins ; RNA-Binding Proteins
    Language English
    Publishing date 2019-07-06
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2071608-4
    ISSN 1568-7856 ; 1568-7864
    ISSN (online) 1568-7856
    ISSN 1568-7864
    DOI 10.1016/j.dnarep.2019.102642
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: The Role of Indoleamine-2,3-Dioxygenase in Cancer Development, Diagnostics, and Therapy.

    Hornyák, Lilla / Dobos, Nikoletta / Koncz, Gábor / Karányi, Zsolt / Páll, Dénes / Szabó, Zoltán / Halmos, Gábor / Székvölgyi, Lóránt

    Frontiers in immunology

    2018  Volume 9, Page(s) 151

    Abstract: Tumors are composed of abnormally transformed cell types and tissues that differ from normal tissues in their genetic and epigenetic makeup, metabolism, and immunology. Molecular compounds that modulate the immune response against neoplasms offer ... ...

    Abstract Tumors are composed of abnormally transformed cell types and tissues that differ from normal tissues in their genetic and epigenetic makeup, metabolism, and immunology. Molecular compounds that modulate the immune response against neoplasms offer promising new strategies to combat cancer. Inhibitors targeting the indoleamine-2,3-dioxygenase 1 enzyme (IDO1) represent one of the most potent therapeutic opportunities to inhibit tumor growth. Herein, we assess the biochemical role of IDO1 in tumor metabolism and immune surveillance, and review current diagnostic and therapeutic approaches that are intended to increase the effectiveness of immunotherapies against highly aggressive and difficult-to-treat IDO-expressing cancers.
    MeSH term(s) Animals ; Humans ; Indoleamine-Pyrrole 2,3,-Dioxygenase/physiology ; Neoplasms/diagnosis ; Neoplasms/enzymology ; Neoplasms/therapy
    Chemical Substances Indoleamine-Pyrrole 2,3,-Dioxygenase
    Language English
    Publishing date 2018-01-31
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2606827-8
    ISSN 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2018.00151
    Database MEDical Literature Analysis and Retrieval System OnLINE

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