AI Article Synopsis

  • Osteosarcoma (OS) is a common childhood cancer with varying survival rates, where around 10%-20% of patients have metastatic disease at diagnosis, leading to a lower survival rate.
  • A study explored DNA methylation in 34 OS samples and identified a three-gene panel (AIM1, p14ARF, and ESR1) that could serve as a prognostic indicator for OS, especially noting p14ARF hypermethylation's link to non-metastatic cases.
  • The findings suggest that promoter methylation is frequent in OS, and specific gene alterations may help predict disease outcomes for patients.

Article Abstract

Osteosarcoma (OS) is the eighth most common form of childhood and adolescence cancer. Approximately 10%-20% of patients present metastatic disease at diagnosis and the 5-year overall survival remains around 70% for nonmetastatic patients and around 30% for metastatic patients. Metastatic disease at diagnosis and the necrosis grade induced by preoperative treatment are the only well-established prognostic factors for osteosarcoma. The DNA aberrant methylation is a frequent epigenetic alteration in humans and has been described as a molecular marker in different tumor types. This study evaluated the DNA aberrant methylation status of 18 genes in 34 OS samples without previous chemotherapy treatment and in four normal bone specimens and compared the methylation profile with clinicopathological characteristics of the patients. We were able to define a three-gene panel (AIM1, p14ARF, and ESR1) in which methylation was correlated with OS cases. The hypermethylation of p14ARF showed a significant association with the absence of metastases at diagnoses, while ESR1 hypermethylation was marginally associated with worse overall survival. This study demonstrated that aberrant promoter methylation is a common event in OS and provides evidence that p14ARF and ESR1 hypermethylation could be useful as a prognostic indicator for this disease.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699305PMC
http://dx.doi.org/10.2147/OTT.S44918DOI Listing

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