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  1. Article ; Online: Changes in the Number of Residual γH2AX Foci in Ki-67-Positive and Ki-67-Negative Human Fibroblasts Irradiated with X-Rays in Doses of 2-10 Gy.

    Vorobyeva, N Yu / Osipov, A A / Chigasova, A K / Yashkina, E I / Osipov, A N

    Bulletin of experimental biology and medicine

    2023  Volume 175, Issue 4, Page(s) 450–453

    Abstract: We studied changes in the number of residual γH2AX foci in cultured human fibroblasts with different expression of the cell proliferation marker protein Ki-67 24, 48, and 72 h after exposure to X-ray radiation in doses of 2-10 Gy. It was shown that, ... ...

    Abstract We studied changes in the number of residual γH2AX foci in cultured human fibroblasts with different expression of the cell proliferation marker protein Ki-67 24, 48, and 72 h after exposure to X-ray radiation in doses of 2-10 Gy. It was shown that, regardless of the expression of Ki-67, the number of residual γH2AX foci in irradiated cells linearly depends on the absorbed dose of X-ray radiation. However, the quantitative yield of residual γH2AX foci per unit of the absorbed dose in Ki-67
    MeSH term(s) Humans ; X-Rays ; Ki-67 Antigen/genetics ; Ki-67 Antigen/metabolism ; Histones/genetics ; Histones/metabolism ; DNA Repair ; Dose-Response Relationship, Radiation ; Fibroblasts/metabolism
    Chemical Substances Ki-67 Antigen ; Histones
    Language English
    Publishing date 2023-09-28
    Publishing country United States
    Document type Journal Article
    ZDB-ID 390407-6
    ISSN 1573-8221 ; 0007-4888 ; 0365-9615
    ISSN (online) 1573-8221
    ISSN 0007-4888 ; 0365-9615
    DOI 10.1007/s10517-023-05883-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Increased Yield of Residual γH2AX Foci in p53-Deficient Human Lung Carcinoma Cells Exposed to Subpicosecond Beams of Accelerated Electrons.

    Vorobyeva, N Yu / Babayan, N S / Grigoryan, B A / Sargsyan, A A / Khondkaryan, L G / Apresyan, L S / Chigasova, A K / Yashkina, E I / Guryev, D V / Rodneva, S M / Tsishnatti, A A / Fedotov, Yu A / Arutyunyan, R M / Osipov, A N

    Bulletin of experimental biology and medicine

    2022  Volume 172, Issue 6, Page(s) 756–759

    Abstract: We studied quantitative yield of residual (24 h post-irradiation) phosphorylated histone (γH2AX) foci as a marker of DNA double strand breaks in wild-type A549 and p53-deficient H1299 human lung carcinoma cells after exposure to subpicosecond (energy 4 ... ...

    Abstract We studied quantitative yield of residual (24 h post-irradiation) phosphorylated histone (γH2AX) foci as a marker of DNA double strand breaks in wild-type A549 and p53-deficient H1299 human lung carcinoma cells after exposure to subpicosecond (energy 4 MeV, pulse duration 400 fsec, peak dose rate during the pulse 16 GGy/s) and quasi-continuous (energy 3.6 MeV) beams of accelerated electrons in a dose range of 0.5-10.0 Gy. The efficiency of pulse irradiation in A549 and H1299 cells assessed by the yield of residual foci was higher than the efficiency of quasi-continuous exposure by 1.8 and 5.3 times, respectively. Significant differences in quantitative yield of residual γH2AX foci between wild-type and p53-deficient cell lines were observed only after exposure to subpicosecond, but not quasi-continuous beams of accelerated electrons.
    MeSH term(s) DNA Breaks, Double-Stranded ; DNA Repair ; Electrons ; Histones/genetics ; Histones/metabolism ; Histones/radiation effects ; Humans ; Lung Neoplasms/genetics ; Lung Neoplasms/metabolism ; Lung Neoplasms/radiotherapy ; Tumor Suppressor Protein p53/deficiency ; Tumor Suppressor Protein p53/genetics ; Tumor Suppressor Protein p53/metabolism
    Chemical Substances Histones ; TP53 protein, human ; Tumor Suppressor Protein p53
    Language English
    Publishing date 2022-05-02
    Publishing country United States
    Document type Journal Article
    ZDB-ID 390407-6
    ISSN 1573-8221 ; 0007-4888 ; 0365-9615
    ISSN (online) 1573-8221
    ISSN 0007-4888 ; 0365-9615
    DOI 10.1007/s10517-022-05472-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Colony-Forming Ability and Residual Foci of DNA Repair Proteins in Human Lung Fibroblasts Irradiated with Subpicosecond Beams of Accelerated Electrons.

    Babayan, N S / Guryev, D V / Vorobyeva, N Yu / Grigoryan, B A / Tadevosyan, G L / Apresyan, L S / Chigasova, A K / Yashkina, E I / Rodneva, S M / Tsishnatti, A A / Fedotov, Yu A / Sarkisyan, N K / Manukyan, A T / Aroutiounian, R M / Osipov, A N

    Bulletin of experimental biology and medicine

    2021  Volume 172, Issue 1, Page(s) 22–25

    Abstract: We performed a comparative study of the colony-forming ability and the number of residual foci of DNA repair proteins in cultured human lung fibroblasts (MRC-5 cell line) after exposure to subpicosecond beams of accelerated electrons with an energy of 3 ... ...

    Abstract We performed a comparative study of the colony-forming ability and the number of residual foci of DNA repair proteins in cultured human lung fibroblasts (MRC-5 cell line) after exposure to subpicosecond beams of accelerated electrons with an energy of 3.6 MeV and quasi-continuous radiation (accelerated electrons with an energy of 4 MeV and X-rays). The yield of damages causing reproductive cell death after pulsed subpicosecond radiation exposure was higher by ~1.8 times than after quasi-continuous radiation exposure. The quantitative yield of residual γH2AX foci (phosphorylated H2AX histone, a protein marker of DNA double breaks) in cells irradiated with subpicosecond beams of accelerated electrons was shown to be ~2.0- 2.5-fold higher than in cells irradiated with quasi-continuous beams of accelerated electrons.
    MeSH term(s) Cell Death/radiation effects ; Cell Line ; Cell Proliferation/radiation effects ; DNA Breaks, Double-Stranded/radiation effects ; DNA Repair Enzymes/metabolism ; Electrons ; Fibroblasts/radiation effects ; Histones/metabolism ; Humans ; Lung/cytology ; Lung/radiation effects
    Chemical Substances H2AX protein, human ; Histones ; DNA Repair Enzymes (EC 6.5.1.-)
    Language English
    Publishing date 2021-11-18
    Publishing country United States
    Document type Journal Article
    ZDB-ID 390407-6
    ISSN 1573-8221 ; 0007-4888 ; 0365-9615
    ISSN (online) 1573-8221
    ISSN 0007-4888 ; 0365-9615
    DOI 10.1007/s10517-021-05323-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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