Sungtae Lee
Yonsei University · Medicine
About the Lab
Professor Sungtae Lee's research lab focuses on translational and molecular oncology, with a strong emphasis on hematopoietic stem cell transplantation, epigenetic regulation in B-cell development, and the genetic and molecular basis of hematologic malignancies and early-onset epilepsy. The lab integrates next-generation sequencing, epigenomic profiling, and clinical biomarker discovery to identify novel therapeutic targets and improve diagnostic accuracy in cancer and neurological disorders. Key research directions include the role of mesenchymal stem cells in haploidentical transplantation, DNA methylation dynamics in lymphoid tumorigenesis, and the clinical utility of BRAF mutation detection in thyroid cancer.
Research Overview
Research Output Trend
Figures are computed from collected data and may differ slightly.
Selected Papers
15A 20-year-old woman with high-risk acute myelogenous leukaemia was transplanted with granulocyte colony stimulating factor (G-CSF)-mobilized peripheral blood CD34+ haematopoietic stem cells and bone-marrow-derived mesenchymal stem cells (MSC) from her human leucocyte antigen haplotype-mismatched father after myeloablative conditioning therapy. The patient engrafted rapidly and had no acute or chronic graft-versus-host disease. Since transplantation, the patient has shown an enduring trilineage h
The epigenetic changes during B-cell development relevant to both normal function and hematologic malignancy are incompletely understood. We examined DNA methylation and RNA expression status during early B-cell development by sorting multiple replicates of four separate stages of pre-B cells derived from normal human fetal bone marrow and applied high-dimension DNA methylation scanning and expression arrays. Features of promoter and gene body DNA methylation were strongly correlated with RNA ex
CONTEXT: Detection of the BRAF V600E mutation in fine-needle aspiration cytology (FNAC) specimens may increase the value of FNAC. OBJECTIVE: The objectives of the study was to compare the diagnostic performance of BRAF assays that differ in sensitivity and to examine the associations between the BRAF V600E mutation status and the clinicopathological features in papillary thyroid carcinoma (PTC). DESIGN AND SETTING: Three molecular assays were performed in all subjects and compared with regard to
We could not convincingly replicate most of the previous studies, a result that is possibly due to modest association between the suggested genes. Rather, we found a new candidate gene, ABCB1, for treatment response, which may provide a hypothesis on the relationship between the blood-brain distribution of CLZ and its clinical efficacy.
BACKGROUND: We intended to evaluate diagnostic utility of a targeted gene sequencing by using next generation sequencing (NGS) panel in patients with intractable early-onset epilepsy (EOE) and find the efficient analytical step for increasing the diagnosis rate. METHODS: We assessed 74 patients with EOE whose seizures started before 3 years of age using a customized NGS panel that included 172 genes. Single nucleotide variants (SNVs) and exonic and chromosomal copy number variations (CNVs) were
The epigenetic landscape of cancer includes both focal hypermethylation and broader hypomethylation in a genome-wide manner. By means of a comprehensive genomic analysis on 6637 tissues of 21 tumor types, we here show that the degrees of overall methylation in CpG island (CGI) and demethylation in intergenic regions, defined as 'backbone', largely vary among different tumors. Depending on tumor type, both CGI methylation and backbone demethylation are often associated with clinical, epidemiologi
We investigated DNA methylomes of pediatric B-cell acute lymphoblastic leukemias (B-ALLs) using whole-genome bisulfite sequencing and high-definition microarrays, along with RNA expression profiles. Epigenetic alteration of B-ALLs occurred in two tracks: de novo methylation of small functional compartments and demethylation of large inter-compartmental backbones. The deviations were exaggerated in lamina-associated domains, with differences corresponding to methylation clusters and/or cytogeneti
This paper presents a detailed experimental study on the sulfate attack of mortar specimens with or without silica fume exposed to sulfate and sulfate–chloride solutions (with the same concentration of SO 4 2– ions) up to 510 d. The overall aim of the study is to investigate the beneficial effect of chloride ions on sulfate attack. In addition, the role of silica fume and water–binder ratio (w/b) in resisting sulfate attack is also reported. To qualitatively assess the performance of mortar spec
This paper describes the resistance of mortar specimens with two different recycled fine aggregates when they were exposed to sodium and magnesium sulfate solutions up to 15months. The important difference between the recycled fine aggregates used in this study was the water absorption. Control mortar specimen made with only river sand was also tested to compare the degree of deterioration by sulfate attack. The tests include visual examination, compressive strength ratio, expansion and mass los
This plate assay is convenient and easy to perform, rapid, and more adaptable for screening of a large number of samples, compared with other existing methods in the literature.
Research Areas
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