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个人简介

教育背景 2001.09—2005.07 上海交通大学 学士学位 2005.09—2010.07 中国科学院生物物理研究所 博士学位 工作经历 2010.07—2012.07 重庆大学生命科学研究院 讲师 2012.07—2017.09 重庆大学生命科学学院 讲师 2017.09— 重庆大学生命科学学院 副教授 学术兼职 重庆市生物化学与分子生物学学会理事 科研项目 主持国家自然基金青年项目1项,教育部博士点新教师基金1项,中央高校科研业务经费面上项目1项。

研究领域

研究原核生物免疫系统及其与机体免疫系统的互作关系。

近期论文

查看导师新发文章 (温馨提示:请注意重名现象,建议点开原文通过作者单位确认)

1. Zhang J, Huang X, Hou Y, Xia X, Zhu Z, Huang A, Feng S, Li P, Shi L*, Dong P*. Isolation and Screening of Antagonistic Endophytes against Phytophthora infestans and Preliminary Exploration on Anti-oomycete Mechanism of Bacillus velezensis 6-5. Plants. 2023; 12(4):909. (*Corresponding author) 2. Li M, Kaili D, Shi L*. Biomarkers for response to immune checkpoint inhibitors in gastrointestinal cancers. World J Gastrointest Oncol. 2022 Jan 15;14(1):19-37. (*Corresponding author) 3. Shi L, Liu Y, Li M, Luo Z. Emerging roles of ferroptosis in the tumor immune landscape: from danger signals to anti-tumor immunity. FEBS J. 2021 May 27. 4. Huang R, Zhou L, Chi Y, Wu H, Shi L*. LncRNA profile study reveals a seven-lncRNA signature predicts the prognosis of patients with colorectal cancer. Biomark Res. 2020 Feb 28;8:8. (*Corresponding author) 5. Qian Y, Shi L*, Luo Z*. Long Non-coding RNAs in Cancer: Implications for Diagnosis, Prognosis, and Therapy. Front Med (Lausanne). 2020 Nov 30;7:612393. (*Corresponding author) 6. Zhao Z, Zhang C, Zhou L, Dong P*, Shi L*. Neurotoxicities associated with immune checkpoint inhibitor therapy. Curr Neuropharmacol. 2020 Dec 30. (*Corresponding author) 7. Shi, L.*, Yu, L., Zou, F., Hu, H., Liu, K., & Lin, Z.* (2017). Gene expression profiling and functional analysis reveals that p53 pathway-related gene expression is highly activated in cancer cells treated by cold atmospheric plasma-activated medium. Peerj, 5:e3751. *Corresponding author 8. Shi L*, Zhang W, Zou F, Mei L, Wu G, Teng Y*. KLHL21, a novel gene that contributes to the progression of hepatocellular carcinoma. BMC Cancer. 2016 Oct 21;16(1):815. *Corresponding author 9. Shi L, Wu L, Wang S, Fan Z. Granzyme F induces a novel death pathway characterized by Bid-independent cytochrome c release without caspase activation. Cell Death and Differentiation 2009 Dec;16(12):1694-706. 10. Zhang H, Zhong C, Shi L, Guo Y, Fan Z. Granulysin induces cathepsin B release of lysosomes of target tumor cells to target mitochondria through processing of Bid. Journal of Immunology 2009; 182(11):6993-7000. 11. D Hu, S Liu, L Shi, L Wu, C Li, Z Fan. Cleavage of survivin by Granzyme M triggers degradation of the survivin-XIAP complex to free caspase activity leading to cytolysis of target tumor cells. Journal of Biological Chemistry 2010 Jun 11;285(24):18326-35. 12. Guo Y*, Chen J*, Shi L, Fan Z. Valosin-containing protein cleavage by granzyme K accelerates an endoplasmic reticulum stress leading to caspase-independent cytotoxicity of target tumor cells. Journal of Immunology 2010; 185(9):5348-59. (*equal contribution) 13. Wang S, Xia P, Shi L, Fan Z. FADD cleavage by NK cell granzyme M enhances its self-association to facilitate procaspase-8 recruitment for auto-processing leading to caspase cascade. Cell Death and Differentiation 2011; 19(4): p.605-15. 14. Shi, GQ, QY Yu, L Shi, Z Zhang*. Molecular cloning and characterization of peroxiredoxin 4 involved in protection against oxidative stress in the silkworm Bombyx mori. Insect Mol Biol 2012; 21: 581-92

学术兼职

重庆市生物化学与分子生物学学会理事

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