Publications by authors named "Sulgi Lee"

Article Synopsis
  • Children with brain tumors face the highest mortality rates among pediatric cancers, with particularly poor outcomes for aggressive types like H3K27M diffuse midline glioma.
  • Recent molecular studies have identified recurrent driver mutations in these tumors, but challenges in obtaining tissues for research persist.
  • A comprehensive protocol for collecting postmortem brain tumor specimens has been developed, successfully yielding xenograft models and insights into tumor behavior, highlighting the critical role of these donations in advancing research and treatment options.
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Anaplastic astrocytomas are aggressive glial cancers that present poor prognosis and high recurrence. Heterozygous IDH1 R132H mutations are common in adolescent and young adult anaplastic astrocytomas. In a majority of cases, the IDH1 R132H mutation is unique to the tumor, although rare cases of anaplastic astrocytoma have been described in patients with mosaic IDH1 mutations (Ollier disease or Maffucci syndrome).

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Complications associated with upfront and repeat surgical tissue sampling present the need for minimally invasive platforms capable of molecular sub-classification and temporal monitoring of tumor response to therapy. Here, we describe our dPCR-based method for the detection of tumor somatic mutations in cell free DNA (cfDNA), readily available in patient biofluids. Although limited in the number of mutations that can be tested for in each assay, this method provides a high level of sensitivity and specificity.

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Diffuse intrinsic pontine gliomas (DIPGs) are deadly tumors comprising 10%-15% of all childhood CNS cancers. Standard treatment is considered palliative and prognosis is near universal mortality. DIPGs have been classified into genomic subtypes based on histone variants with the lysine to methionine mutation on position 27 of histone tails (K27M).

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