李枫 教授
职称职务:教授,博导,系主任
学科专业:医学遗传学
研究方向:肿瘤靶向治疗
实验室位置:澳门新葡游戏网11号楼
Email: fli222@whu.edu.cn
学习经历
1998.09~2002.07 华中农业大学,攻读学士学位
2002.09~2008.01 华中农业大学&中国科学院生 物物理研究所联合培养,硕博连读
主要工作经历与任职
2008.04~2013.04 University of Kentucky College of Medicine, 博士后
2013.06~至今 武汉大学医学遗传学系,教授、博导
目前主要科学研究领域和兴趣
目前研究方向为肿瘤靶向治疗,鉴定新的靶点和提出新的治疗手段,包括
1. 基于肿瘤表观遗传的靶向治疗研究;
2. 肿瘤细胞信号通路蛋白复合物的鉴定和功能研究;
3. 新型亚细胞结构的发生机制与病理生理功能研究
教学情况
先后主讲过《医学遗传学》(中文/英文),细胞生物学,基础医学导论,博士英语等。参编国家卫计委“十三五”规划教材《医学遗传学(英文)》(人民卫生出版社)。
代表性论文
1.Yan Lin, Mingkun Yang, Li Huang, Fan Yang, Jiachen Fan, Yulong Qiang, Yuting Chang, Wenjie Zhou, Leilei Yan, Jie Xiong, Jie Ping, Shizhen Chen, Dong Men* and Feng Li*. A bacteria-derived tetramerized protein ameliorates nonalcoholic steatohepatitis (NASH) in mice via binding and relocating acetyl-coA carboxylase. Cell Reports, (2023), Nov 16; 42(11):113453.
2. Wenting Pan, Yihao Tian , Qian Zheng , Zelin Yang , Yulong Qiang , Zun Zhang , Nan Zhang , Jie Xiong* , Xin Zhu* , Lei Wei * and Feng Li *. Oncogenic BRAF noncanonically promotes tumor metastasis by mediating VASP phosphorylation and filopodia formation. Oncogene, (2023), Oct; 42(43):3194-3205.
3. Guanlan Fan#, Fan Wang#, Yurou Chen , Qian Zheng , Jie Xiong , Qiongying Lv , Kejia Wu , Jiaqiang Xiong , Lei Wei , Dongqing Li , Jiachen Zhang , Wei Zhang* and Feng Li* .The deubiquitinase OTUD1 noncanonically suppresses Akt activation through its N-terminal intrinsically disordered region. Cell Reports, (2023), Jan 31; 42(1):111916.
4. Qian Zheng#, Pengfei Li#, Xin Zhou, Yulong Qiang, Jiachen Fan, Yan Lin, Yurou Chen, Jing Guo, Fan Wang, Haihua Xue, Jie Xiong* and Feng Li*. Deficiency of the X-inactivation escaping gene KDM5C in clear cell renal cell carcinoma promotes tumorigenicity by reprogramming glycogen metabolism and inhibiting ferroptosis. Theranostics , (2021) 11(18): 8674-8691.
5.Chen X#, Zhao B#, Qu Y, Chen Y, Xiong J, Feng Y, Men D, Huang Q, Liu Y, Yang B, Ding J and Feng Li*. Detectable Serum Severe Acute Respiratory Syndrome Coronavirus 2 Viral Load (RNAemia) Is Closely Correlated With Drastically Elevated Interleukin 6 Level in Critically Ill Patients With Coronavirus Disease 2019;Clinical Infectious Disease. (2020) 71(8):1937–42. 注: 该研究为SCI高被引论文。
6.向莹,熊洁,李枫* 肿瘤细胞中染色质修饰与代谢的相互调控, 肿瘤代谢与营养电子杂志 , 2019年12月9日第6卷第4期.
7. Ying Xiang, Kai Yan, Qian Zheng, Haiqiang Ke, Jie Cheng, Wenjun Xiong, Xin Shi, Lei Wei, Min Zhao, Fei Yang, Ping Wang, Xing Lu, Li Fu, Xuemei Lu*, and Feng Li*.Histone demethylase KDM4B promotes DNA damage by activating long interspersed nuclear element-1. Cancer Research, (2019),79(1),86-98.
8. Xiaohua Chen, Loo JX, Shi X, Xiong W, Guo Y, Ke H, Yang M, Jiang Y, Xia S, Zhao M, Zhong S, He C, Fu L, and Feng Li*. E6 Protein Expressed by High-Risk HPV Activates Super-Enhancers of the EGFR and c-MET Oncogenes by Destabilizing the Histone Demethylase KDM5C, Cancer Research, (2018),78(6),1418-1430.
9. Feng Li, J.Ortega, B.Peng, Gu, L., and Li,G.M*. Regulation of Mismatch Repair by Histone Code and Posttranslational Modifications in Eukaryotic Cells (Review). DNA Repair, (2016), 68–74.
10. Feng Li, Mao, G.G., Tong, D., Huang,J., Gu, L. *, and Li,G.M*, The histone mark H3K36me3 regulate human mismatch repair through its interaction with MutSalpha, Cell, 2013, 153, 590–600. 注: 该研究为SCI高被引论文。