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Faculty
Tsai-Kun Li, Ph.D.

Affiliation:

Department of Microbiology

National Taiwan University

E-mail address: tsaikunli@ntu.edu.tw

Detail PDF

 

URL:https://scholars.lib.ntu.edu.tw/cris/rp/rp06152

 

Academic History:

-(1991)Department of Microbiology

  BD in Microbiology

  Soochow University, Taiwan, ROC

-(1999)Department of Pharmacology,

  PhD in Pharmacology

  Rutgers University & University of Medicine and Dentistry of New Jersey, USA

 

Professional/Scientific Career:

 

1987- 1990

Voluntary Research Assistant

Soochow University, Taiwan, ROC

1993- 1994

Research Assistant  

Institute of Molecular Biology
Academia Sinica, Taiwan, ROC

1999- 2003

Postdoctoral Fellow

Rutgers University & University of Medicine and Dentistry of New Jersey, USA

2000- 2003

Research Teaching Specialist

Rutgers University & University of Medicine and Dentistry of New Jersey, USA

2001- 2001

Visiting Scientist

Institute of Molecular Biology
Academia Sinica, Taiwan, ROC

2003- 2007

Assistant Professor

Dept. & Graduate Institute of Microbiology, National Taiwan University, Taiwan, ROC

2007- 2011

Associate Professor

Dept. & Graduate Institute of Microbiology,
National Taiwan University, Taiwan, ROC

2008- Now

Principal Investigator

Center for Biotechnology
National Taiwan University, Taiwan, ROC

2008- Now

Chief

Division of Research and Development,
Center for Biotechnology,
National Taiwan University, Taiwan, ROC

2011- Now

Professor

School of Integrative and Global Majors,
University of Tsukuba, Tsukuba, Japan

2011- Now

Professor

Dept. & Graduate Institute of Microbiology,
National Taiwan University, Taiwan, ROC

2012- Now

Director

Office for International Affairs, NTUCM,
National Taiwan University, Taiwan, ROC

2012- Now

Associate Dean

College of Medicine,
National Taiwan University, Taiwan, ROC

2015- Now

Associate Editor

Journal "Genes to Cell", Japan

2015- Now

PI

NTU SPARK Program,
Taiwan Supra Integration and Incubation Center

2015- Now

CEO

NTU Center for Genome Medicine,
National Taiwan University, Taiwan, ROC

 

 

Awards/Professional Societies:
Topoisomerases, Topoisomerase-targeting drugs, DNA damage and repair.
• DNA topology and its biological implications
• Topoisomerases and their targeting drugs
• Repair and signaling pathways for DNA damage
 
Research Area/ Interests:
The research conducted in my laboratory combines both molecular and biochemical approaches toward investigating the following interrelated programs of research: 
 
Roles of DNA topoisomerases in DNA organization: Topoisomerases are ubiquitous, essential nuclear enzymes that participate in the regulation of DNA different topological states by transient breakage and rejoining of DNA. Cellular functions of different topoisomerases are currently under investigation.
Studies on topoisomerase-mediated DNA damage: Due to its delicate act of breaking/rejoining DNA, topoisomerase is highly vulnerable while performing its enzymatic reaction on DNA. In agreement with this notion, DNA topoisomerases have been firmly established as highly effective molecular targets for antibiotics (e.g. quinolones) and anti-tumor drugs (e.g. camptothecins). Our lab also interested in understanding the molecular determinants for topoisomerase-targeting conditions.
Post-translational modification of DNA topoisomerases: Modification and proteolytic pathways have been suggested to participate in regulating functions and activities of DNA topoisomerases. For example, ubiqutin/26S proteasome pathway has been implicated to degrade topoisomerases from cleavable complexes. 
 
Publications  * corresponding author
Selected publications (Original article, ; Review,  ) 
1. Yeh Y-H, Wang S-W, Yeh Y-C, Hsiao H-F, Li T-K* (2016) Rhapontigenin inhibits TGF--mediated epithelial‑mesenchymal transition via the PI3K/AKT/mTOR pathway and is not associated with HIF-1 degradation Oncol Rep. May, 35(5): 2887-95.
2. Chou S-M, Lai W-J, Hong T, Tsai S-H, Chen Y-H, Kao C-H, Chu R, Shen T-L*, Li T-K* (2015) Involvement of p38 MAPK in the Anticancer Activity of Cultivated Cordyceps militaris. Am. J. Chin. Med. 43(5): 1043-57.
3. Hsieh M-Y, Fan J.R., Chang H-W, Chen H-C, Shen T.-L., Teng SC, Yeh Y-H, Li T-K*. (2014) DNA topoisomerase IIIalpha cooperates with p53 in senescence and tumor-suppression. Clinical Cancer Research. 20(6): 1489-501.
4. Yeh Y-H, Yang Y-C, Hsieh M-Y, Yeh Y-C, Li T-K*. (2013) A negative feedback of the HIF-1 pathway via interferon-stimulated gene 15 and ISGylation. Clinical Cancer Research, 19(21): 5927-39.
5. Wu, C-C, Li, T-K*, Farh L, Lin LY, Lin TS, Yu YJ, Yen TJ, Chiang CW and Chan NL. (2011) Structural basis of type II topoisomerase inhibition by the anticancer drug etoposide. Science. 333:459-62.