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Article

Overall survival of classical Hodgkin's lymphoma in Saudi patients is affected by XPG repair gene polymorphism

  • Authors:
    • Huda Al Sayed Ahmed
    • Wasim Fawzi Raslan
    • Abdel Halim Salem Deifalla
    • Mohammad Dahmani Fathallah
  • View Affiliations / Copyright

    Affiliations: Pathology Services Division and Laboratory Department, Johns Hopkins Aramco Healthcare, Dhahran 34465, Kingdom of Saudi Arabia, Department of Anatomy, College of Medicine and Medical Sciences, Arabian Gulf University, Manama 26671, Kingdom of Bahrain, Department of Higher Studies, Arabian Gulf University, Manama 26671, Kingdom of Bahrain
  • Pages: 10-16
    |
    Published online on: October 30, 2018
       https://doi.org/10.3892/br.2018.1165
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Abstract

In Hodgkin's lymphoma (HL), single nucleotide polymorphisms (SNPs) of specific DNA repair genes have been identified to have an important role in the risk of HL. Consequently, they may also serve an important role in HL prognosis and disease outcome. The present study aimed to define an SNP molecular profile, based on DNA repair genes mutations, as predictive biomarkers for the prognostic outcome of patients with Classical HL (CHL) in Saudi Arabia. Genotyping of selected SNPs located in selected DNA repair genes was performed on 100 CHL cases and an equivalent number of healthy controls. No significant associations between CHL disease relapse (DR) or overall survival (OS) and 4 DNA repair genes were observed, with the exception of xeroderma pigmentosum, complementation group G (XPG) repair gene SNP (rs17655), which revealed a statistically significant association with CHL patient survival (P=0.036). Accordingly, these data suggest that the XPG gene may be a useful predictive molecular genetic biomarker for CHL clinical outcome. The present study also provided valuable insights on the contribution of DNA repair genes in Saudi patients with CHL. To the best of our knowledge, we defined for the first time, a specific genetic pattern associated with CHL outcome was defined in the present study in Saudi patients.
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Copy and paste a formatted citation
Spandidos Publications style
Al Sayed Ahmed H, Raslan WF, Deifalla AH and Fathallah MD: Overall survival of classical Hodgkin's lymphoma in Saudi patients is affected by XPG repair gene polymorphism. Biomed Rep 10: 10-16, 2019.
APA
Al Sayed Ahmed, H., Raslan, W.F., Deifalla, A.H., & Fathallah, M.D. (2019). Overall survival of classical Hodgkin's lymphoma in Saudi patients is affected by XPG repair gene polymorphism. Biomedical Reports, 10, 10-16. https://doi.org/10.3892/br.2018.1165
MLA
Al Sayed Ahmed, H., Raslan, W. F., Deifalla, A. H., Fathallah, M. D."Overall survival of classical Hodgkin's lymphoma in Saudi patients is affected by XPG repair gene polymorphism". Biomedical Reports 10.1 (2019): 10-16.
Chicago
Al Sayed Ahmed, H., Raslan, W. F., Deifalla, A. H., Fathallah, M. D."Overall survival of classical Hodgkin's lymphoma in Saudi patients is affected by XPG repair gene polymorphism". Biomedical Reports 10, no. 1 (2019): 10-16. https://doi.org/10.3892/br.2018.1165
Copy and paste a formatted citation
x
Spandidos Publications style
Al Sayed Ahmed H, Raslan WF, Deifalla AH and Fathallah MD: Overall survival of classical Hodgkin's lymphoma in Saudi patients is affected by XPG repair gene polymorphism. Biomed Rep 10: 10-16, 2019.
APA
Al Sayed Ahmed, H., Raslan, W.F., Deifalla, A.H., & Fathallah, M.D. (2019). Overall survival of classical Hodgkin's lymphoma in Saudi patients is affected by XPG repair gene polymorphism. Biomedical Reports, 10, 10-16. https://doi.org/10.3892/br.2018.1165
MLA
Al Sayed Ahmed, H., Raslan, W. F., Deifalla, A. H., Fathallah, M. D."Overall survival of classical Hodgkin's lymphoma in Saudi patients is affected by XPG repair gene polymorphism". Biomedical Reports 10.1 (2019): 10-16.
Chicago
Al Sayed Ahmed, H., Raslan, W. F., Deifalla, A. H., Fathallah, M. D."Overall survival of classical Hodgkin's lymphoma in Saudi patients is affected by XPG repair gene polymorphism". Biomedical Reports 10, no. 1 (2019): 10-16. https://doi.org/10.3892/br.2018.1165
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