Academic Staff > G.S.W. Tsao

 

George S. W. Tsao ( 曹世華 )
Professor and Head of Department
B.Sc.(H.K.), Ph.D.(Lond.), CBiol, MIBiol.

Department of Anatomy
1/F. Laboratory Block
Faculty of Medicine Building
21 Sassoon Road, Hong Kong

Anatomy Office: (852) 2819-9227 (voice)
Anatomy Office: (852) 2817-0857 (fax)

E-mail: gswtsao@hkucc.hku.hk

Jump to: Background / Research / Publications / Collaborations

Background

Educational Background and Previous Appointment:

Ph.D (Institute of Cancer Research, Royal Marsden Hospital, University of London); Lecturer (Chinese University of Hong Kong); Postdoctoral Research Fellow (Dana Farber Cancer Institute, Harvard Medical School); Instructor (Dana Farber Cancer Institute, Harvard Medical School); Assistant Professor (Brigham and Women's Hospital, Harvard Medical School); Laboratory Director (Laboratory of Gynecologic Oncology, Brigham and Women's Hospital, Harvard Medical School).

Current Appointments:

Professor, Department of Anatomy, University of Hong Kong
Director, Center of Cancer Research, Faculty of Medicine, University of Hong Kong
Assistant Dean (Research), Faculty of Medicine, University of Hong Kong
Honorary Director, Center for Cellular Biology, University of Hong Kong

International Advisory Board:

Board member of Epstein-Barr virus Association (elected in 2006)

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Research

Research Interests:
Cancer cell biology, nasopharyngeal carcinoma, Epstein-Barr virus biology, cell immortalization and tumorigenesis, mitotic checkpoint dysregulation, chromosome instability, live cell imaging

Current Research Topics:
Molecular basis of cell immortalization and human carcinogenesis; EBV infection and pathogenesis of nasopharyngeal carcinoma; genomic instability in cells and mitotic checkpoint dysregulation, esophageal carcinoma

Summary of Research:
My laboratory is interested in the elucidation of major molecular and cellular events involved in human carcinogenesis

Nasopharyngeal carcinoma
We are defining the genetic elements involved in immortalization and malignant transformation of primary nasopharyngeal epithelial cells. A panel of immortalized nasopharyngeal epithelial cell lines has been established. The functional roles of specific genetic and cellular events identified in premalignant nasopharyngeal epithelium are examined. Among these events is the infection of EBV which is believed to play an etiological role in carcinogenesis in nasopharyngeal carcinoma. EBV infection of these premalignant nasopharyngeal epithelial cell models have been achieved.

EBV infection is closely associated with nasopharyngeal carcinoma. The EBV DNA could be detected in practically all NPC cells. The EBV encoded oncogenes may functionally interact with genetic alterations present in precancerous nasopharyngeal lesions converting them into invasive cancers. The oncogenic potential of EBV genes and their effects on cell signaling mechanisms leading to deregulation of cell growth, escape from senescence, resistance to apoptosis and development of invasive properties are under current investigation using immortalized nasopharyngeal epithelial cell models established in my laboratory.

Esophageal carcinoma
We have established immortalized esophageal cell models from Hong Kong and areas in mainland China with high risk esophageal carcinoma. The functional role of specific genetic events involved in immortalization and malignant transformation of normal esophageal epithelium will be defined.

Genomic instability in tumorigenesis
Immortalized epithelial cell models from nasopharyangeal and epithelial origins have been established in our laboratory. These immortalized epithelial cells are used to investigate major invents lending to mitotic dysregulation and chromosome instability and their contribution to tumorigenesis.

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Selected Publications

(from over 200 international and peer-reviewed manuiscripts)

*Principal/corresponding author


Man, C., Rosa, J., Yip, Y. L., Cheung, A. L., Kwong, Y. L., Doxsey, S. J., and *Tsao, S. W. Id1 overexpression induces tetraploidization and multiple abnormal mitotic phenotypes by modulating aurora A. Molecular Biology of Cell, 19: 2389-2401, 2008.

Deng, W., Tsao, S. W., Kwok, Y. K., Wong, E., Huang, X. R., Liu, S., Tsang, C. M., Ngan, H. Y., Cheung, A. N., Lan, H. Y., Guan, X. Y., and Cheung, A. L. Transforming growth factor beta1 promotes chromosomal instability in human papillomavirus 16 E6E7-infected cervical epithelial cells. Cancer Research, 68: 7200-7209, 2008.

Choy EY, Siu KL, Kok KH, Lung RW, Tsang CM, To KF, Kwong DL, Tsao SW, Jin DY. An Epstein-Barr virus-encoded microRNA targets PUMA to promote host cell survival. Journal of Experimental Medicine, 205(11):2551-60, 2007.

Man, C., Rosa, J., Lee, L. T., Lee, V. H., Chow, B. K., Lo, K. W., Doxsey, S., Wu, Z. G., Kwong, Y. L., Jin, D. Y., Cheung, A. L., and *Tsao, S. W. Latent membrane protein 1 suppresses RASSF1A expression, disrupts microtubule structures and induces chromosomal aberrations in human epithelial cells. Oncogene, 26: 3069-3 2007.

Li, H. M., Man, C., Jin, Y., Deng, W., Yip, Y. L., Feng, H. C., Cheung, Y. C., Lo, K. W., Meltzer, P. S., Wu, Z. G., Kwong, Y. L., Yuen, A. P., and *Tsao, S. W. Molecular and cytogenetic changes involved in the immortalization of nasopharyngeal epithelial cells by telomerase. International Journal of Cancer, 119: 1567-1576, 2006.

Tsai, C. L., Li, H. P., Lu, Y. J., Hsueh, C., Liang, Y., Chen, C. L., Tsao, S. W., Tse, K. P., Yu, J. S., and Chang, Y. S. Activation of DNA methyltransferase 1 by EBV LMP1 Involves c-Jun NH(2)-terminal kinase signaling. Cancer Research, 66: 11668-11676, 2006.

Li HM, Zhuang ZH, Wang Q, Pang JC, Wang XH, Wong HL, Feng HC, Jin DY, Ling MT, Wong YC, Eliopoulos AG, Young LS, Huang DP, *Tsao SW. Epstein-Barr virus latent membrane protein 1 (LMP1) upregulates Id1 expression in nasopharyngeal epithelial cells. Oncogene, 23(25):4488-94, 2004.

Deng W, Tsao SW, Guan XY, Lucas JN, Si HX, Leung CS, Mak P, Wang LD, Cheung AL. Distinct profiles of critically short telomeres are a key determinant of different chromosome aberrations in immortalized human cells: whole-genome evidence from multiple cell lines. Oncogene, 23(56):9090-101, 2004.

Lo AK, Huang DP, Lo KW, Chui YL, Li HM, Pang JC, *Tsao SW. Phenotypic alterations induced by the Hong Kong-prevalent Epstein-Barr virus-encoded LMP1 variant (2117-LMP1) in nasopharyngeal epithelial cells. International Journal of Cancer. 109(6):919-25, 2004.

Lo AKF, Liu Y, Wang XH, Huang DP, Yuen PW, Wong YC and *Tsao SW. Alterations of biologic properties and gene expression in nasopharyngeal epithelial cells by the Epstein-Barr virus-encoded latent membrane protein 1. Laboratory Investigation, 83, 697-709, 2003.

Wong X., Jin D.Y., Wong H.L., Feng H., Wong Y.C. and *Tsao S.W. MAD2-induced sensitization to vincristine is associated with mitotic arrest and Raf/Bcl-2 phosphorylation in nasopharyngeal carcinoma cells. Oncogene, 22, 109-116, 2003.

*Tsao S.W. Tramoutanis G, Dawson C.W, Lo AKF and Huang D.P. The significance of LMP1 expression in nasopharyngeal carcinoma. Seminars in Cancer Biology, 474-487, 2003.

Wang X., Jin D.Y., Ng R.W., Feng H., Wong Y.C., Cheung A.L.M., *Tsao S.W. Significance of MAD2 expression to mitotic checkpoint control in ovarian cancer cells. Cancer Research, Vol 62, 1662-8, 2002.

Wang X.H., Jin D.Y., Wong Y.C., Cheung A.L.M., Chun A.C.S., Lo A.K.F., Liu Y. and *Tsao S.W. Correlation of defective mitotic checkpoint with aberrantly reduced expression of MAD2 protein in nasopharyngeal carcinoma cells. Carcinogenesis, Vol 21, 2293-2297, 2000.

Wang X.H., Wong S.C.H, Pan J., Tsao S.W., Fung K.H.Y, Kwong D.L.W, Sham J.S.T. and Nicholls J.M. Evidence of cisplastin-induced senescent-like growth arrest in nasopharyngeal carcinoma cells. Cancer Research,  Vol 58: 5019-5022, 1998.

He D., Zhang D.K., Lam K.Y., Ma L., Ngan H.Y.S., Liu S.S., *Tsao S.W. Prevalence of HPV infection in esophageal squamous cell carcinoma in Chinese Patients and its relationship to the p53 gene mutation. International Journal of Cancer, Vol 72, 959-964, 1997.

*Tsao S.W., Mok S.C.H., Fey E., Fletcher J., Wan T.S.K., Chew E.C., Michael G. M., Knapp R.C., Berkowitz R.S. Immortalization and characterization of an human ovarian surface epithelial cell line. Experimental Cell Research,  Vol 218, 499-507, 1995.

Mok S.C.H., Bell D.A., Knapp R.C., Fishbaugh P.M., Welch W.R., Muto M.G. Berkowitz R.S. and *Tsao S.W. Mutation of K-ras protooncogene in human ovarian epithelial tumors of borderline malignancy. Cancer Research, Vol 53, 1489-1492, 1993.

Mok C.H., *Tsao S.W., Knapp R.C., Fishbaugh P. and Lau C.C. Unifocal origin of advanced human epithelial ovarian cancers. Cancer Research, Vol 52, 5119-5122, 1992.

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Collaborations

International:
Professor Steve Doxsey, University of Massachusetts, USA
Professor Gary Gorbsky, University of Oklahoma, USA
Professor Kenzo Takada, University of Hokkaido, Japan
Professor Lawrence Young, University of Birmingham, UK

National:
Professor Zeng YX, Cancer Center, Sun Yat-Sen University, Guangzhou, PR China
Professor Zeng MS, Cancer Center, Sun Yat-Sen Univeristy, Guangzhou, PR China
Professor Cao Y, Cancer Research Institute, XiangYa School of Medicine, Central South University, Changsha, Hunan, PR China

Hong Kong:
Prof M. Lung, Dept. of Clinical Oncology, HKU
Dr. ALM Cheung, Dept. of anatomy, HKU
Professor HYS Ngan, Dept. of Obstetrics & Gynaecology, HKU
Professor ANY Cheung, Dept. of Pathology, HKU
Dr. DY Jin, Dept. of Biochemistry, HKU
Dr. YB Feng, School of Chinese Medicine, HKU


Dr. ZG Wu, Dept. of Biochemistry, HKUST
Professor. Randy Poon, Dept. of Biochemistry, HKUST

Professor KW Lo, Anatomical and Cellular Pathology, CUHK
Professor Qian Tao, Dept. of Clinical Oncology, CUHK
Professor Vivien Liu, Dept. of Clinical Oncology, CUHK
 

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