Home / People / / Jun Dai

Jun Dai ——Associate Professor

Nationality:
CHINA
Phone:
022-87401830
Email:
jun.dai@tju.edu.cn
Office:
Room A303, Building 24, Tianjin University
School:
School of Pharmaceutical Science and Technology
ResearcherID:
Group weblink
Education Experience
2000 Ph. D. Tulane University, LA
2000 Postdoctoral Brigham and Womens Hospital, Boston, MA
Professional Experience
2008-2014 Instructor in Dermatology Massachusetts General Hospital/Harvard Medical School
2005-2008 Instructor in Medicine Brigham and Women’s Hospital/Harvard Medical School
2000-2005 Postdoctoral Fellow Brigham and Women’s Hospital, Boston, MA
Research Area

The research efforts of the Dai group encompass two areas:  1) The role of retinoid-related orphan receptor RORα in controlling skin homeostatis, and 2) Control of normal mitosis by protein kinase haspin.  In the first area, the main interest is on the interplay between intra- and inter-cellular signaling pathways involved in control of skin tissue homeostasis and tumor development. Focuses on the role of the nuclear orphan receptor RORα in controlling keratinocyte differentiation and skin tumor formation, as well as the therapeutic potential of RORα agonists/antagonists in treatment of skin diseases.  In the second area, the group is interested in exploring the role of haspin in cancer development and the potential of haspin inhibitors as anti-tumor drugs.

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Honors and Awards
Patents
Highlighted Publications
Dai, J.; Brooks, Y.; Lefort, K.; Getsios, S.; Dotto, G. P. The retinoid-related orphan receptor RORα promotes keratinocyte differentiation via FOXN1. PLoS ONE 2013, 8, e70392.
Wang, F.; Dai, J.; Daum, J. R.; Niedzialkowska E.; Banerjee B.; Stukenberg T.; Gorbsky G. J.; Higgins, J. M. Histone H3 Thr-3 phosphorylation by haspin positions Aurora B at centromeres in mitosis. Science 2010, 330, 231.
Dai, J.; Kateneva, A. V.; Higgins, J. M. Studies of haspin-depleted cells reveal that spindle-pole integrity in mitosis requires chromosome cohesion. J. Cell Sci. 2009, 122, 4148.
Dai, J.; Sullivan, B. A.; Higgins, J. M. Regulation of mitotic chromosome cohesion by haspin and aurora B. Dev. Cell 2006; 11, 741. (Featured cover illustration)
Dai, J.; Sultan, S.; Taylor, S. S.; Higgins, J. M. The kinase haspin is required for mitotic histone H3 Thr 3 phosphorylation and normal metaphase chromosome alignment. Genes & Dev. 2005, 19, 472. (Featured cover illustration)
ResearcherID Publications
Year Title Author(s) Source Volume
2004 ACAP1 promotes endocytic recycling - Short article by recognizing recycling sorting signals Dai, J; Li, J; Bos, E; et al. Developmental Cell 7
2002 Involvement of the mt1 melatonin receptor in human breast cancer Ram, PT; Dai, J; Yuan, L; et al. Cancer Letters 179
2002 Modulation of intracellular calcium and calmodulin by melatonin in MCF-7 human breast cancer cells Dai, J; Inscho, EW; Yuan, L; et al. Journal of Pineal Research 32
2002 MT1 melatonin receptor overexpression enhances the growth suppressive effect of melatonin in human breast cancer cells Yuan, L; Collins, AR; Dai, J; et al. Molecular and Cellular Endocrinology 192
2002 Tumor prevention by 9-cis-retinoic acid in the N-nitroso-N-methylurea model of mammary carcinogenesis is potentiated by the pineal hormone melatonin Nowfar, S; Teplitzky, SR; Melancon, K; et al. Breast Cancer Research and Treatment 72
2001 Chemoprevention of NMU-induced rat mammary carcinoma with the combination of melatonin and 9-cis-retinoic acid Teplitzky, SR; Kiefer, TL; Cheng, Q; et al. Cancer Letters 168
2001 Transcriptional repression of RORalpha activity in human breast cancer cells by melatonin. Dai, J; Ram, P T; Yuan, L; et al. Molecular and cellular endocrinology 176
2000 Differential responsiveness of MCF-7 human breast cancer cell line stocks to the pineal hormone, melatonin Ram, PT; Yuan, L; Dai, J; et al. Journal of Pineal Research 28
Determining if a test compound inhibits haspin kinase activity, comprises incubating a solution comprising haspin and a polypeptide, for phosphorylation; and determining test compound the inhibits phosphorylation of the polypeptide HIGGINS J M G; DAI J
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