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蔡振宇,同济大学医学院教授,美国德州农工大学生物医学专业博士,美国国立卫生研究院访问学者。获国家海外高人层次青年人才,主持国家自然科学基金和上海市科技创新基金等科研项目。主要从事坏死性凋亡的分子机制及其相关肿瘤炎症性疾病的研究,发现坏死性凋亡的关键分子机制,揭示了坏死性凋亡在乳腺癌发生发展中的作用和机制,自主建立了抗坏死性凋亡小分子药物筛选平台,鉴定并发现了一系列具有抗坏死活性的临床候选化合物。课题组主要研究方向:(1)坏死性死亡及其所诱发的炎症反应与肿瘤发生发展的关系(主要以乳腺癌、肝癌和结肠癌为肿瘤模型);(2)抗坏死性死亡小分子药物筛选、鉴定与临床应用;(3)坏死性凋亡的分子调控机理。研究成果以通讯作者或第一作者发表在Nat Cell Biol, Cell Research,PNAS, Cancer Research, Br J Pharmacol, J Med Chem等杂志。其中2篇的研究论文入选ESI前1%高被引论文,专利授权4项。
1 Rui C,Shi SN, Ren W, Qin X, Zhuang C, Chen X, Chen G, Yu J, Wang HY, Cai Z. Themultitargeted kinase inhibitor KW-2449 ameliorates cisplatin-inducednephrotoxicity by targeting RIPK1-mediated necroptosis. BiochemPharmacol. 2021,188:114542.
2 Qin X†,Hu L†, Shi SN†, Chen X, Zhuang C, Zhang W, Jitkaew S,Pang X, Yu J, Tan YX#, Wang HY#, Cai Z#. The Bcr-Abl inhibitor GNF-7 inhibits necroptosis and amelioratesacute kidney injury by targeting RIPK1 and RIPK3 kinases. BiochemPharmacol. 2020,177:113947.
3 Qin X,Ma D, Tan Y#, Wang H#, Cai Z#. The role of necroptosis in cancer: a double-edgedsword? Biochim Biophys Acta Rev Cancer, 2019,1871:259-266. (#, Correspondence author) (Review)
4 Chen X†,Zhuang C†,#,Ren Y†, Zhang H, Qin X, Hu L, Fu J, Miao Z, Chai Y, Liu Z, Cai Z#,Wang H# , Identification of TAK-632 and its analogues as potent inhibitors ofnecroptosis by targeting RIPK1 and RIPK3, 2019, Br J Pharmacol,176(12):2095-2108. (#, Correspondence author; †, equal contribution)
5 Cai Z,Zhang A, Choksi S, Li W, Li T, Zhang X, and Liu Z. Activation of cell surfaceproteases promotes necroptosis, inflammation and cell migration. CellResearch, 2016, 26(8):886-900.
6 Cai Z†,Jitkaew S†, Zhao J†, Chiang H, Choksi S, LiuJ, Ward E, Wu L, Liu Z. Plasma membrane translocationof trimerized MLKL protein is required for TNF-induced necroptosis. NatCell Biol. 2014; 16(1):55-65. (†, equal contribution) (ESI Highly Cited Paper)
7 Zhao J†, Jitkaew S†, Cai Z†, Choksi S, Li Q, Luo J, Liu ZG. Mixed lineage kinasedomain-like is a key receptor interacting protein 3 downstream component ofTNF-induced necrosis. Proc Natl Acad Sci U S A. 2012;109(14):5322-7. (†, equal contribution) (ESIHighly Cited Paper)
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