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机构概况 |
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研究队伍 |
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姓 名: |
缪泽鸿 |
性 别: |
男 |
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职 称: |
研究员 |
学 历: |
博士 |
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电 话: |
021-50806820 |
传 真: |
021-50806820 |
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电子邮件: |
zhmiao@mail.shcnc.ac.cn |
个人主页: |
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通讯地址: |
上海市浦东新区祖冲之路555号 201203 |
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| 简历: |
1988年、1996年和2003年分别毕业于华西医科大学医学专业、中国医学科学院中国协和医科大学肿瘤研究所药理学专业和中国科学院上海药物研究所药理学专业,获医学学士学位、医学硕士学位和理学博士学位;1988年至2000年在四川泸州医学院先后任药理学助教、讲师、副教授;2004年至2006年在美国国立卫生研究院国家癌症研究所(NIH、NCI)做博士后;2003年至今先后任中国科学院上海药物研究所副研究员、研究员、博士生导师、研究组长;兼任中国抗癌协会抗癌药物专业委员会委员/秘书长、中国药理学会肿瘤药理专业委员会委员/秘书长、Acta Pharmacol Sin编委等。 |
| 研究方向: |
肿瘤药理学。从事抗肿瘤新药研究研发及抗肿瘤作用机制研究,着重围绕肿瘤DNA损伤修复、缺氧、异常转录和耐药展开创新型抗肿瘤药物发现及相关机制研究。 |
| 职务: |
| 中国科学院上海药物研究所博士生导师、研究员 |
| 承担科研项目情况: |
- 抗肿瘤药物早期成药性评价关键技术研究。国家重大新药创制重大专项关键技术研究(编号:2012ZX09301-001-002),2012.1-2015.12
- 新型PARP-1抑制剂的设计优化和成药性研究。国家重大新药创制重大专项创新药物研究开发(编号:2012ZX09103-101-071),2012.1-2015.12
- 新型纳米药物降低肝癌细胞耐药性的机制和药效学研究。国家重大科学研究计划项目(编号:2012CB932502),2012.1-2016.8
- 抗癌药物药理。国家杰出青年科学基金(编号:81025020),2011.1-2014.12
- 新型有丝分裂抑制剂MT7分子靶标的发现、确证及分子机制研究。国家自然基金面上项目(编号:30873092),2009.1-2011.12
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| 获奖及荣誉: |
- 国家杰出青年基金获得者(2010)
- 入选中国科学院“百人计划”(2010)
- 国家自然科学奖二等奖(2009)
- 药明康德生命化学研究奖三等奖(2009)
- 入选上海市浦江人才计划(2008)
- 上海市自然科学奖一等奖(2007)
- 全国百篇优秀博士论文奖(2005)
- 中国科学院院长特别奖(2004)
- 中国科学院优秀博士学位论文(2004)
- 上海药学科技一等奖(2004)
- 中国药理学会Servier奖(2003)
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| 代表论著: |
- Zhao-Li Zhou, Ya-Xi Yang, Jian Ding, Yuan-Chao Li*, Ze-Hong Miao*. Triptolide: structural modifications, structure-activity relationship, bioactivities, clinical development and mechanisms. Nat Prod Rep. 2011 (Invited review; in press)
- Bing Yu, Mei-Hong Li, Wei Wang, Ying-Qing Wang, Yi Jiang, Sheng-Ping Yang, Jian-Min Yue, Jian Ding*, Ze-Hong Miao*. Pseudolaric acid B-driven phosphorylation of c-Jun impairs its role in stabilizing hypoxia inducible factor-1alpha: a novel function-converter model. J Mol Med. 2011 (in press).
- Yi Jiang, Ze-Hong Miao*, Bing Yu, Lei Xu, Jing-Xu Gong, Lin-Jiang Tong, Yi Chen, Zhao-Li Zhou, Hong-Chun Liu, Yi Wang, Yue-Wei Guo, Jian Ding*. Drug-transporter-independent liver cancer cell killing by a marine steroid methyl spongoate via apoptosis induction. J Biol Chem. 2011; 286:26461- 26469.
- Yuqin Wang, Qian He, Xiao-Hua Li, Yi Chen, Yuyuan Xie, Jian Ding, Ze-Hong Miao*, Chunhao Yang*. Design, synthesis and biological evaluation of substituted 11H-benzo[]carbazole-5-carboxamide as novel antitumor agents. Eur J Med Chem.2011; 46: 5878-5884.
- Zhixiang Zhang, Tao Meng, Na Yang, Wei Wang, Bing Xiong, Yi Chen, Lanping Ma, Jingkang Shen, Ze-Hong Miao*, Jian Ding*. MT119, a new planar-structured compound, targets the colchicine site of tubulin arresting mitosis and inhibiting tumor cell proliferation. Int J Cancer. 2011; 129:214-224.
- Jin-xue He, Chun-hao Yang, Ze-hong Miao*. PARP inhibitors as promising cancer therapeutics. Acta Pharmacol Sin. 2010;31:1172-1180. (Invited review)
- Zhao-Li Zhou, Zhi-Guo Luo, Bing Yu, Yi Jiang, Yi Chen, Jian-Ming Feng, Mei Dai, Lin-Jiang Tong, Zheng Li, Yuan-Chao Li, Jian Ding, Ze-Hong Miao*. Increased accumulation of hypoxia-inducible factor-1α with reduced transcriptional activity mediates the antitumor effect of triptolide. Mol Cancer. 2010;9:268pp1-11.
- Ming Li, Ze-Hong Miao*, Zhi Chen, Qin Chen, Min Gui, Li-Ping Lin, Peng Sun, Yang-Hua Yi, Jian Ding*. Echinoside A, a new marine-derived anticancer saponin, targets topoisomerase II by unique interference with its DNA binding and catalytic cycle. Ann Oncol. 2010;21:597-607.
- Mei Dai, Ze-Hong Miao*, Xuan Ren, Lin-Jiang Tong, Na Yang, Ting Li, Li-Ping Lin, Yue-Mao Shen, Jian Ding*. MFTZ-1, a novel topoisomerase II poison, reduces constitutive and inducible HIF-1α accumulation and VEGF secretion irrelevant to its topoisomerase II inhibition. J Cell Mol Med. 2010; 10: 2281–2291.
- Zhixiang Zhang, Tao Meng, Jingxue He, Ming Li, Lin-Jiang Tong, Bing Xiong, Liping Lin, Jingkang Shen, Ze-Hong Miao* and Jian Ding*. MT7, a novel compound from a combinatorial library, arrests mitosis via inhibiting the polymerization of microtubules. Invest New Drug. 2010; 28:715-728.
- Bing Yu, Ze-Hong Miao*, Yi Jiang, Mei-Hong Li, Na Yang, Ting Li, Jian Ding*. c-Jun protects HIF-1 from degradation via its Oxygen-Dependent-Degradation domain in a non-transcriptional manner. Cancer Res. 2009; 69:7704-7712.
- Hong Zhu, Ze-Hong Miao*, Min Huang, Jian-Ming Feng, Zhi-Xiang Zhang, Yu-Jun Cai, Lin-Jiang Tong, Xu-Hong Qian, Yu-Fang Xu, Jian Ding*. Naphthalimides induce G2 phase arrest in HCT-116 cells via ATM-activated Chk2-executed pathway. Neoplasia. 2009; 11: 1226–1234.
- Jian-Ming Feng, Hong Zhu, Xiao-Wei Zhang, Jian Ding, Ze-Hong Miao*. Proteasome-dependent degradation of Chk1 kinase induced by the topoisomerase II inhibitor R16 contributes to its anticancer activity. Cancer Biol Ther. 2008, 7: 1726-1731.
- Ze-Hong Miao, Audrey Player, Uma Shankavaram, Yong-Hong Wang, Drazen Zimonjic, PhilipLorenzi,Zhi-Yong Liao, Hong Liu,Tsutomu Shimura,Hong-Liang Zhang,Ling-Hua Meng, Yong-Wei Zhang,Ernest S. Kawasaki, Nicholas C. Popescu, Mirit I. Aladjem, David Goldstein, John Weinstein, Yves Pommier*. Non-Classical Functions of Human Topoisomerase I:Genomewide and Pharmacological Analyses. Cancer Res. 2007; 67:8752-61.
- Jian Ding*, Ze-Hong Miao, Ling-Hua Meng, Mei-Yu Geng. Emerging cancer therapeutic opportunities target DNA repair systems. Trends Pharmacol Sci (TiPS). 2006; 27:338-344. (Invited review).
- Ze-Hong Miao, V. Ashutosh Rao, Keli Agama, Smitha Antony, Yves Pommier*. 4-Nitroquinoline-1-oxide induces the formation of cellular Topoisomerase I-DNA cleavage complexes. Cancer Res. 2006; 66: 6540-6545.
- Ze-Hong Miao, Keli Agama, Olivier Sordet, Lawrence Povirk, Kurt W. Kohn, Yves Pommier*. Defective repair of topoisomerase I cleavage complexes in hereditary ataxia SCAN1 cells. DNA Repair. 2006; 5:1489-94.
- Ze-Hong Miao, Lin-Jiang Tong, Jin-Sheng Zhang, Jia-Xian Han, Jian Ding*. Characterization of salvicine-resistant lung adenocarcinoma A549/SAL cell line. Int J Cancer. 2004; 110: 627–632.
- Ze-Hong Miao, Jian Ding*. Transcription factor c-Jun activation represses mdr-1 gene expression. Cancer Res. 2003; 63: 4527-4532.
- Ze-Hong Miao, Tao Tang, Yi-Xiang Zhang, Jin-Sheng Zhang, Jian Ding*. Cytotoxicity, apoptosis induction and downregulation of mdr-1 expression by the anti-topoisomerase II agent, salvicine, in multidrug-resistant cells. Int J Cancer. 2003; 106:108-115.
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