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Article

IDH1 mutation of gliomas with long-term survival analysis

  • Authors:
    • Jae Kyung Myung
    • Hwa Jin Cho
    • Chul-Kee Park
    • Seung-Ki Kim
    • Ji Hoon Phi
    • Sung-Hye Park
  • View Affiliations / Copyright

    Affiliations: Department of Pathology, Seoul National University Hospital, College of Medicine, Seoul, Republic of Korea, Department of Neurosurgery, Seoul National University, College of Medicine, Seoul, Republic of Korea, Department of Pediatric Neurosurgery, Seoul National University Children's Hospital, College of Medicine, Seoul, Republic of Korea
  • Pages: 1639-1644
    |
    Published online on: August 24, 2012
       https://doi.org/10.3892/or.2012.1994
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Abstract

A recurrent mutation affecting codon 132 of the isocitrate dehydrogenase 1 (IDH1) gene has been found in ~5% of primary glioblastomas (GBMs), but in >70% of secondary GBMs or oligodendroglial and astrocytic tumors. We investigated IDH1 mutations in a series of 134 brain tumors to determine the prevalence and prognostic impact of IDH1 mutations. We also examined the correlations among histology, p53 and PTEN immunoexpression, MGMT methylation status, 1p 19q co-deletion and EGFR gene amplification. The 134 brain tumors included 41 low-grade oligodendrogliomas (LOs), 47 anaplastic oligodendrogliomas (AOs) and 46 primary GBMs. Data showed that 53.7% (72/134) of cases showed mutations affecting codon 132 of IDH1, including 73.2% of LOs, 82.9% of AOs and three primary GBMs (6.5%). All IDH1 mutations were Arg132His. In a survival analysis, patients with IDH1 mutations had better survival compared to those with wild-type IDH1 (p<0.05) in LOs and AOs, but not in primary GBMs (p=0.587). In addition, in patients with both IDH1 mutation and MGMT methylation, p53 overexpression was a significant poor prognostic factor both in LOs and AOs. However, IDH1 mutation was not correlated with common genetic profiles that affect patient prognosis, including MGMT methylation, 1p 19q co-deletion, PTEN loss and EGFR amplification in LOs, AOs and GBMs. From our results, IDH1 mutation was an independent positive prognostic factor in LOs and AOs, especially in the absence of p53 overexpression.
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Copy and paste a formatted citation
Spandidos Publications style
Myung JK, Cho HJ, Park C, Kim S, Phi JH and Park S: IDH1 mutation of gliomas with long-term survival analysis. Oncol Rep 28: 1639-1644, 2012.
APA
Myung, J.K., Cho, H.J., Park, C., Kim, S., Phi, J.H., & Park, S. (2012). IDH1 mutation of gliomas with long-term survival analysis. Oncology Reports, 28, 1639-1644. https://doi.org/10.3892/or.2012.1994
MLA
Myung, J. K., Cho, H. J., Park, C., Kim, S., Phi, J. H., Park, S."IDH1 mutation of gliomas with long-term survival analysis". Oncology Reports 28.5 (2012): 1639-1644.
Chicago
Myung, J. K., Cho, H. J., Park, C., Kim, S., Phi, J. H., Park, S."IDH1 mutation of gliomas with long-term survival analysis". Oncology Reports 28, no. 5 (2012): 1639-1644. https://doi.org/10.3892/or.2012.1994
Copy and paste a formatted citation
x
Spandidos Publications style
Myung JK, Cho HJ, Park C, Kim S, Phi JH and Park S: IDH1 mutation of gliomas with long-term survival analysis. Oncol Rep 28: 1639-1644, 2012.
APA
Myung, J.K., Cho, H.J., Park, C., Kim, S., Phi, J.H., & Park, S. (2012). IDH1 mutation of gliomas with long-term survival analysis. Oncology Reports, 28, 1639-1644. https://doi.org/10.3892/or.2012.1994
MLA
Myung, J. K., Cho, H. J., Park, C., Kim, S., Phi, J. H., Park, S."IDH1 mutation of gliomas with long-term survival analysis". Oncology Reports 28.5 (2012): 1639-1644.
Chicago
Myung, J. K., Cho, H. J., Park, C., Kim, S., Phi, J. H., Park, S."IDH1 mutation of gliomas with long-term survival analysis". Oncology Reports 28, no. 5 (2012): 1639-1644. https://doi.org/10.3892/or.2012.1994
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