首页 全所PI名录
  • 高大明
  • 研究员,研究组长,博士生导师
  • E-mail: dgao@@sibcb.ac.cn
  • 实验室主页: 
    个人简介:
  •   2001年毕业于山东大学,获学士学位;2006年毕业于中科院生化与细胞所,获博士学位。2006年12月至2012年7月于美国哈佛医学院/以色列女执事医学中心(Harvard Medical School/Beth Israel Deaconess Medical Center)从事博士后研究。2012年7月底回国就任中国科学院生物化学与细胞生物学研究所研究员,研究组长。

    社会任职:
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    研究方向:
  • 癌症信号转导与代谢
    研究工作:
  •   肿瘤细胞的一个重要特征是近乎无限的分裂增殖。这种表型可能由多种生理过程的异常所引起,包括细胞周期负调因子的缺失突变、细胞代谢途径的超常活跃、关键信号通路的活化及细胞凋亡通路的异常等。本实验室的研究兴趣主要集中于调控肿瘤细胞生长增殖的核心信号转导与细胞代谢调节机制方面,特别是发现关键信号蛋白的重要转录后修饰,从而诠释肿瘤细胞生长增殖/癌症发生发展的分子机制,并为癌症的临床治疗提供新的思路与治疗靶点。

    承担科研项目情况:
    代表论著:
    1. Cui B#, Gong L#, Chen M, Zhang Y, Yuan H, Qin J, Gao D*. CUL5-SOCS6 complex regulates mTORC2 function by targeting Sin1 for degradation. Cell Discov. 2019 Oct 29;5:52. doi: 10.1038/s41421-019-0118-6. eCollection 2019.
    2. Gao Q#, Zhu H#, Dong L#, Shi W#, Chen R#, Song Z, Huang C, Li J, Dong X, Zhou Y, Liu Q, Ma L, Wang X, Zhou J, Liu Y, Boja E, Robles A, Ma W, Wang P, Li Y, Ding L, Wen B, Zhang B, Rodriguez H, Gao D*, Zhou H*, Fan J*. Integrated Proteogenomic Characterization of HBV-related Hepatocellular Carcinoma. Cell. 2019, 179: 561–577
    3. Kuai X#, Li L#, Chen R, Wang K, Chen M, Cui B, Zhang Y, Li J, Zhu H, Zhou H, Huang J, Qin J, Wang Z, Wei W, Gao D*. SCFFBXW7/GSK3β-mediated GFI1 degradation suppresses gastric cancer cell proliferation. Cancer Res. 2019 doi: 10.1158/0008-5472.CAN-18-4032. 
    4. Zhao G#, Gong L#, Su D#, Jin Y, Guo C, Yue M, Yao S, Qin Z, Ye Y, Tang Y, Wu Q, Zhang J, Cui B, Ding Q, Huang H, Hu L, Chen Y, Zhang P, Hu G, Chen L, Wong KK, Gao D*, Ji H*.Cullin5 deficiency promotes small-cell lung cancer metastasis by stabilizing integrin β1. J Clin Invest. 2019, 129(3):972-987.
    5. Xie X, Hu H, Tong X, Li L, Liu X, Chen M, Yuan H, Xie X, Li Q, Zhang Y, Ouyang H, Wei M, Huang J, Liu P, Gan W, Liu Y, Xie A, Kuai X, Chirn GW, Zhou H, Zeng R, Hu R, Qin J, Meng FL, Wei W, Ji H, Gao D*  The mTOR-S6K pathway links growth signalling to DNA damage response by targeting RNF168.Nat Cell Biol. 2018, 20(3):320-331. doi: 10.1038/s41556-017-0033-8.
    6. Liu X, Chen M, Li L, Gong L, Zhou H, Gao D*. ERK kinases phosphorylate Lin28a to modulate P19 cell proliferation and differentiation. J Biol Chem. 2017, 292(10):3970-3976.
    7. Hu H, Zhu W, Qin J, Chen M, Gong L, Li L, Liu X, Tao Y, Yin H, Zhou H, Zhou L, Ye D, Ye Q, Gao D*. Acetylation of PGK1 promotes liver cancer cell proliferation and tumorigenesis. Hepatology. 2017,65(2):515-528.
    8. Lau AW#, Liu P#, Inuzuka H*, Gao D*. SIRT1 phosphorylation by AMP-activated protein kinase regulates p53 acetylation. Am J Cancer Res. 2014 May 26;4(3):245-55.
    9. Inuzuka H#, Gao D#, Finley LW, Yang W, Wan L, Fukushima H, Chin YR, Zhai B, Shaik S, Lau AW, Wang Z, Gygi SP, Nakayama K, Teruya-Feldstein J, Toker A, Haigis MC, Pandolfi PP, Wei W. Acetylation-dependent regulation of Skp2 function. Cell. 2012 Jul 6;150(1):179-93. (* Co-first author)
    10. Gao D#, Inuzuka I#, Tan M#, Fukushima H, Locasale JW, Liu P, Wan L, Zhai B, Chin YR, Shaik S, Lyssiotis CA, Gygi SP, Toker A, Cantley LC, Asara JM, Harper JW and Wei W. mTOR drives its own activation via SCFβ-TRCP-dependent degradation of the mTOR inhibitor DEPTOR. Mol Cell, 2011, 44(2):290-303. (# Co-first author)
    11. Gao D, Wan L, Inuzuka H, Berg AH, Tseng A, Zhai B, Shaik S, Bennet E, Tron AE, Gasser JA, Lau A, Gygi S, Harper JW, DeCaprio JA, Toker A and Wei W. Rictor forms a complex with Cullin-1 to promote SGK1 ubiquitination and destruction. Mol Cell, 2010, 39: 797-808.
    12. Gao D, Inuzuka H, Korenjak M, Tseng A, Wu T, Wan L, Kirschner M, Dyson N and Wei W. Cdh1 regulates cell cycle through modulating the Claspin/Chk1 and the Rb/E2F1 pathways. Mol Biol Cell, 2009, 20: 3305-3316.
    13. Gao D, Inuzuka H, Tseng A, Chin R, Toker A and Wei W. Phosphorylation by Akt1 promotes cytoplasmic localization of Skp2 and impairs APC/Cdh1-medaited Skp2 destruction. Nat Cell Biol, 2009, 11: 397-408.
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