Duksoo Bae
Sungkyunkwan University · Medicine
About the Lab
Professor Duksoo Bae's research lab focuses on molecular oncology and cancer immunology, with a primary emphasis on identifying key molecular mechanisms underlying cervical and ovarian carcinomas. The lab investigates tumor suppressor genes such as BRD7 and signaling molecules like TLR9, ICAM-3, and sphingosine kinase 1 (SK1) to understand their roles in cancer progression, therapy resistance, and immune modulation. Using in vitro, in vivo, and clinical tissue-based approaches, the lab aims to discover novel biomarkers and therapeutic targets for gynecological cancers.
Research Overview
Research Output Trend
Figures are computed from collected data and may differ slightly.
Selected Papers
15Toll-like receptors (TLRs) recognize pathogen-associated molecular patterns (PAMPs) and enable innate immune responses. Although TLR9 has been previously considered to be expressed only in immune cells, there is now increasing evidence that TLR9 expression is present in nonimmune cells as well. In this study, we undertook to determine whether TLR9 expression was associated with disease progression in cervical neoplasia. TLR9 expression was evaluated by immunohistochemistry in 55 formalin-fixed p
PURPOSE: Bromodomain-containing protein 7 (BRD7), which is a subunit of SWI/SNF complex, has been recently suggested as a novel tumor suppressor in several cancers. In this study, we investigated the tumor suppressive effect of BRD7 in epithelial ovarian cancer. EXPERIMENTAL DESIGN: We analyzed the expression of BRD7 in human ovarian tissues with real-time PCR. To investigate the functional role of BRD7, we transfected ovarian cancer cells (A2780 and SKOV3) with BRD7 plasmid and checked the cell
The RT and RH groups, unlike the CC group, had compromised sexual function after the treatment of early-stage cervical cancer.
To search for a marker that predicts the efficacy of radiation therapy in human cervical cancer, gene expression profiles between parental SiHa cervical cancer cells and radiation-resistant SiHa/R cells have been compared by the microarray technique. Microarray and Northern blot analyses demonstrated that the ICAM-3 expression was upregulated in SiHa/R cells. This increased expression of ICAM-3 in SiHa cells enhanced cell survival by about 34.3% after a 2 Gy dosage of radiation. In addition, SiH
Research Areas
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