menu
Introduction
  • The research goal of the center is to understand stem cell functions and disease mechanisms, in order to develop therapeutics for the treatment of human diseases. The center focuses on the generation of 3D human disease model systems using reprogrammed cells such as patient-derived induced pluripotent stem cells (iPSCs) for developing personalized and in vivo-mimetic disease models. In addition, the center developed an alternative method for animal testing, named as the ¡®Networking Organoid Culture System (NOCS),' which involves different types of organoids, such as the intestine, liver, heart, brain, etc.
Research Areas
  • Development of core technologies involved in the cell fate change between somatic cells and stem cells
  • Modeling 3D human diseases based on stem cells, reprogramming, and organoid technology
  • In silico prediction systems for differentiation or determining the functional status of in vitro models
  • Development of a biomimetic 3D human tissue and networking platform for predicting drug toxicity and efficacy
  • Characterization of genes related to various diseases such as cancer and the development of therapeutic interventions such as small molecules, gene therapy, regenerative cells, and tissues
Head
Investigator
Name Position Tel / Email Detail
Mi-Young Son Associate Director / Detail

Tel

042-860-4426

Email

myson@kribb.re.kr

Achievements
  • Expandable Human Pluripotent Stem Cell-Derived Hepatic Organoids
  • Blockade of STAT3 causes severe in vitro and in vivo maturation defects in intestinal organoids derived from human embryonic stem cells
  • Mass cytometry-based single-cell analysis on reprogramming to human iPSCs
  • Stabilization of E2-EPF UCP protein is implicated in hepatitis B virus-associated hepatocellular carcinoma progression.
Selected Publications
  • Differential effects of EGFL6 on tumor versus wound angiogenesis.
    • Cell Rep. 21(10):2785-2795.
    • Kyung Hee Noh (First)
  • A liver-specific gene expression panel predicts the differentiation status of In vitro hepatocyte models.
    • Hepatology. 66(5):1662-1674.
    • Hyun Soo Cho, Nam-Soon Kim and Cho Rok Jung (Co-corresponding))
  • Distinctive genomic signature of neural and intestinal organoids from familial Parkinson¡¯s disease patient-derived induced pluripotent stem cells.
    • Neuropathol Appl Neurobiol. 43(7):584-603.
    • Janghwan Kim, Cho Rok Jung and Mi Young Son (Co-corresponding)
  • Novel prognostic marker PRMT1 regulates cell growth via downregulation of CDKN1A in HCC.
    • Oncotarget. 8(70):115444-115455.
    • Hyun Soo Cho and Dae Soo Kim (Co-corresponding)
  • Cell spheroids with enhanced aggressiveness to mimic human liver cancer In vitro and In vivo.
    • Sci Rep. 7(1):10499.
    • Cho Rok Jung and Jung Hwa Lim (Co-corresponding)