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ID1 affects the efficacy of radiotherapy in glioblastoma through inhibition of DNA repair pathways.

Abstract
Glioblastoma multiforme (GBM) is characterized by poor therapeutic response and poor overall survival. It is crucial that more effective therapies be developed for the treatment of GBM. Inhibitor of DNA binding protein-1 (ID1) has been shown to maintain the self-renewal capacity of neural stem cells and might be involved in the therapeutic resistance of GBM. In the present study, we explored survival data from the The Cancer Genome Atalas database that were based on ID1 expression for patients diagnosed with primary GBMs. Interestingly, patients with high ID1 expression had better survival than patients with low ID1 expression, and a strong correlation was found between radiotherapy efficacy, ID1 expression, and overall survival. We further investigated the relationship between ID1 expression and the radiosensitivity of glioblastoma using glioblastoma cell lines. The clonogenic formation assay showed that U87 ID1-shRNA cells were much less sensitive to radiation. Moreover, both the results of the γH2AX foci staining assay and the comet assay further revealed that ID1 negatively regulates DNA repair processes by downregulating the expression of genes such as DNA ligase IV (LIG4) and ataxia-telangiectasia-mutated. Additionally, ID1 induces G2/M arrest in U87 cells. Taken together, these results suggest that ID1 may be a new prognostic marker for GBM and have important implications for the therapeutic strategies used to treat GBM patients.
AuthorsQinhua Guo, Pin Guo, Qing Mao, Jin Lan, Yingying Lin, Jiyao Jiang, Yongming Qiu
JournalMedical oncology (Northwood, London, England) (Med Oncol) Vol. 30 Issue 1 Pg. 325 (Mar 2013) ISSN: 1559-131X [Electronic] United States
PMID23377983 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Biomarkers, Tumor
  • ID1 protein, human
  • Inhibitor of Differentiation Protein 1
Topics
  • Biomarkers, Tumor (analysis, genetics)
  • Blotting, Western
  • Brain Neoplasms (genetics, metabolism, radiotherapy)
  • Comet Assay
  • DNA Repair (genetics)
  • Fluorescent Antibody Technique
  • Glioblastoma (genetics, metabolism, radiotherapy)
  • Humans
  • Inhibitor of Differentiation Protein 1 (genetics, metabolism)
  • Kaplan-Meier Estimate
  • Prognosis
  • Proportional Hazards Models
  • Radiation Tolerance (genetics)
  • Real-Time Polymerase Chain Reaction

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