مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

124
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

59
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

Evaluating Gamma-H2AX Expression as a Biomarker of DNA Damage after X-ray in Angiography Patients

Pages

  393-402

Abstract

 Objective: Coronary heart disease (CHD) is one of the most common diseases. Coronary Angiography (CAG) is an important apparatus used to diagnose and treat this disease. Since Angiography is performed through exposure to ionizing radiation, it can cause harmful effects induced by double-stranded breaks in DNA which is potentially life-threatening damage. The aim of the present study is to investigate phosphorylation of Histone H2AX in the location of double-stranded breaks in peripheral blood lymphocytes as an indication of biological effects of radiation on Angiography. Materials and Methods: This method is based on the phosphorylation measurement of Histone (gamma-H2AX or γ-H2AX) levels on serine 139 after the formation of DNA double-strand break. 5 cc of blood samples from 24 patients undergoing Angiography were taken pre-and post-radiation. Blood lymphocytes were extracted, fixed and stained with specific γ-H2AX antibodies. Finally, the percentage of phosphorylation of Histone H2AX as an indicator of double-strand break was measured by a cytometry technique. Results: An increase was observed in all patients’ percentage of phosphorylated Histone H2AX (double-stranded breaks DNA) after radiation (20. 15 ± 14. 18) compared to pre-exposure time (1. 52 ± 0. 34). Also, the mean of DNA double-strand break is shown in a linear correlation with DAP. Discussion: Although induction of DNA double-strand breaks was associated with the radiation dose in patients, the effect of individual factors such as radio-sensitivity and regenerative capacity should not be ignored. In the future, if we are able to measure DNA Damage response in every Angiography patient, we will use it as a biomarker for the patient dose; this will promote public health. Conclusion: Using flow cytometers readings done automatically is possible to detect γ-H2AX in the number of blood cells, therefore, the use of this technique could play a significant role in monitoring patients.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    ALIPOOR, A., FARDID, R., & SHARIFZADEH, S.. (2018). Evaluating Gamma-H2AX Expression as a Biomarker of DNA Damage after X-ray in Angiography Patients. JOURNAL OF BIOMEDICAL PHYSICS AND ENGINEERING, 8(4), 393-402. SID. https://sid.ir/paper/334632/en

    Vancouver: Copy

    ALIPOOR A., FARDID R., SHARIFZADEH S.. Evaluating Gamma-H2AX Expression as a Biomarker of DNA Damage after X-ray in Angiography Patients. JOURNAL OF BIOMEDICAL PHYSICS AND ENGINEERING[Internet]. 2018;8(4):393-402. Available from: https://sid.ir/paper/334632/en

    IEEE: Copy

    A. ALIPOOR, R. FARDID, and S. SHARIFZADEH, “Evaluating Gamma-H2AX Expression as a Biomarker of DNA Damage after X-ray in Angiography Patients,” JOURNAL OF BIOMEDICAL PHYSICS AND ENGINEERING, vol. 8, no. 4, pp. 393–402, 2018, [Online]. Available: https://sid.ir/paper/334632/en

    Related Journal Papers

  • No record.
  • Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button