性 别:

最高学历、学位:博士

职 称:助理研究员

院内职务:

个人简介

浙江大学医学院附属第一医院特聘研究员。在美国圣路易斯华盛顿大学医学院进行博士后训练,主要研究方向为真核细胞内遗传信息质量监控系统的分子调控机制。围绕DNA复制压力下应答机制研究,首次发现细胞通过激活胞浆钙信号来维持停滞复制叉结构稳定性,并发现cGAS-STING通过激活TRPV2介导的内质网钙释放来应答复制压力,揭示了其固有免疫之外的又一非经典功能。利用全基因组CRISPR/Cas9敲除技术,对无义介导的mRNA降解途径(NMD)的调控因子进行了系统性筛选,发现RNA剪切体复合物的多个组分能够促进NMD,靶向NMD关键激酶可作为一种新的合成致死策略治疗由剪接体突变造成的急性髓系白血病。以一作/共同一作在Mol Cell,Nat Commun, Cancer Res等国际学术期刊发表多篇研究论文。


专业擅长

肿瘤学和细胞信号转导


研究方向

肿瘤代谢与DNA损伤修复机制的交互调控机制;

联合免疫疗法与靶向DNA损伤修复途径的肿瘤治疗研究


成果奖项:(近五年主要成果及奖励情况)

承担科研项目:

cGAS/STING非经典功能激活Ca2+信号通路响应DNA复制压力和肿瘤发生的分子机制研究, 国家自然科学基金,面上,2023-01-01至2026-12-31,主持

 

代表性的论文:

1. Shan Li*, Lingzhen Kong*, Ying Meng, Chen Cheng, Delphine Sangotokun Lemacon, Zheng Yang, Ke Tan, Abigael Cheruiyot, Zhimin Lu, Zhongsheng You. Cytosolic DNA sensing by cGAS/STING promotes TRPV2-mediated Ca2+ release to protect stressed replication forks. Molecular Cell, 2023, 83(4): 556-573. (Featured Article) Preview by Jungsan Sohn, Molecular Cell, 2023, 83(4):502-503.

2. Zenan Wang*, Binghao Li*, Shan Li*, Wenlong Lin, Zhan Wang, Shengdong Wang, Weida Chen, Wei Shi, Tao Chen, Hao Zhou, Eloy Yinwang, Wenkan Zhang, Haochen Mou, Xupeng Chai, Jiahao Zhang, Zhimin Lu & Zhaoming Ye (2022) Metabolic control of CD47 expression through LAT2-mediated amino acid uptake promotes tumor immune evasion. Nat Commun. 6308 (2022) (*共同第一作者)

3. Abigael Cheruiyot*, Shan Li*, Sridhar Nonavinkere Srivatsan, Tanzir Ahmed, Yuhao Chen, Del-phine Sangotokun Lemacon, Ying Li, Zheng Yang, Brian A Wadugu, Wayne A. Warner, Shondra M Pruett-Miller, Esther A. Obeng, Daniel C. Link, Dalin He, Fei Xiao, Xiaowei Wang, Julie M Bailis, Matthew J Walter and Zhongsheng You (2021) Nonsense-mediated RNA Decay Is a Unique Vulnerability of Cancer Cells harboring SF3B1 or U2AF1 mutations. Cancer Research. doi: 10.1158/0008-5472.CAN-20-4016(*共同第一作者)

4. Shan Li, Zeno Lavagnino, Delphine Lemacon, Lingzhen Kong, Alessandro Ustione, Xuewen Ng, Yuanya Zhang, Yingchun Wang, Bin Zheng, Helen Piwnica-Worms, Alessandro Vindigni, David W Piston, Zhongsheng You (2019) Ca(2+)-Stimulated AMPK-Dependent Phosphorylation of Exo1 Protects Stressed Replication Forks from Aberrant Resection. Mol Cell 74(6):1123-1137.e6. (Featured Article) Preview by Antoine Simoneau, Lee Zou, Mol Cell, 2019;74(6):1103-1105 


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