Radiosensitivity in lymphoblastoid cell lines derived from Shwachman-Diamond syndrome patients

Radiat Prot Dosimetry. 2015 Sep;166(1-4):95-100. doi: 10.1093/rpd/ncv152. Epub 2015 Apr 12.

Abstract

Shwachman-Diamond syndrome is an autosomal-recessive disorder characterised by bone marrow failure and a cumulative risk of progression to acute myeloid leukaemia. The Shwachman-Bodian-Diamond syndrome (SBDS) gene, the only gene known to be causative of the pathology, is involved in ribosomal biogenesis, stress responses and DNA repair, and the lack of SBDS sensitises cells to many stressors and leads to mitotic spindle destabilisation. The effect of ionising radiation on SBDS-deficient cells was investigated using immortalised lymphocytes from SDS patients in comparison with positive and negative controls in order to test whether, in response to ionising radiation exposure, any impairment in the DNA repair machinery could be observed. After irradiating cells with different doses of X-rays or gamma-rays, DNA repair kinetics and the residual damages using the alkaline COMET assay and the γ-H2AX assay were assessed, respectively. In this work, preliminary data about the comparison between ionising radiation effects in different patients-derived cells and healthy control cells are presented.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Marrow Diseases / genetics*
  • Bone Marrow Diseases / radiotherapy*
  • Comet Assay
  • DNA Damage / radiation effects*
  • DNA Repair / radiation effects*
  • Exocrine Pancreatic Insufficiency / genetics*
  • Exocrine Pancreatic Insufficiency / radiotherapy*
  • Gamma Rays
  • Histones / genetics
  • Humans
  • Kinetics
  • Lipomatosis / genetics*
  • Lipomatosis / radiotherapy*
  • Lymphocytes / radiation effects*
  • Proteins / genetics
  • Proteins / metabolism
  • Radiation Tolerance / genetics*
  • Shwachman-Diamond Syndrome
  • X-Rays

Substances

  • H2AX protein, human
  • Histones
  • Proteins
  • SBDS protein, human