Qun Ying Lei

Summary

Affiliation: Fudan University
Country: China

Publications

  1. ncbi TAZ promotes cell proliferation and epithelial-mesenchymal transition and is inhibited by the hippo pathway
    Qun Ying Lei
    Department of Biological Chemistry, School of Medicine, Molecular and Cellular Biology Laboratory, Institutes of Biomedical Sciences, Department of Biology, School of Life Science, Fudan University, Shanghai 200032, China
    Mol Cell Biol 28:2426-36. 2008
  2. ncbi The N-terminal phosphodegron targets TAZ/WWTR1 protein for SCFβ-TrCP-dependent degradation in response to phosphatidylinositol 3-kinase inhibition
    Wei Huang
    Key Laboratory of Molecular Medicine, Ministry of Education, Department of Biochemistry and Molecular Biology, Shanghai Medical College, Fudan University, Shanghai 200032, China
    J Biol Chem 287:26245-53. 2012
  3. ncbi TEAD transcription factors mediate the function of TAZ in cell growth and epithelial-mesenchymal transition
    Heng Zhang
    Molecular and Cell Biology Laboratory, Institutes of Biomedical Sciences, School of Life Science, Fudan University, Shanghai, China 200032
    J Biol Chem 284:13355-62. 2009
  4. ncbi PP1 cooperates with ASPP2 to dephosphorylate and activate TAZ
    Chen Ying Liu
    Key Laboratory of Molecular Medicine, Ministry of Education, Department of Biochemistry and Molecular Biology School of Medicine, Lab, Institutes of Biomedical Sciences, Fudan University, Shanghai 200032, China
    J Biol Chem 286:5558-66. 2011
  5. ncbi Targeted polyubiquitylation of RASSF1C by the Mule and SCFβ-TrCP ligases in response to DNA damage
    Xin Zhou
    Key Laboratory of Molecular Medicine, Ministry of Education, Department of Biochemistry and Molecular Biology, Shanghai Medical College, Shanghai 200032, China
    Biochem J 441:227-36. 2012
  6. ncbi The relationship between PTEN expression and anoikis in human lung carcinoma cell lines
    Qun Ying Lei
    Key Laboratory of Glycoconjugate Research, Ministry of Health, Biochemistry Department, Fudan University Medical College, Shanghai 200032, China
    Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai) 34:463-8. 2002
  7. ncbi Acetylation targets the M2 isoform of pyruvate kinase for degradation through chaperone-mediated autophagy and promotes tumor growth
    Lei Lv
    Key Laboratory of Molecular Medicine, Ministry of Education, Department of Biochemistry and Molecular Biology, Fudan University, Shanghai 200032, China
    Mol Cell 42:719-30. 2011

Collaborators

Detail Information

Publications7

  1. ncbi TAZ promotes cell proliferation and epithelial-mesenchymal transition and is inhibited by the hippo pathway
    Qun Ying Lei
    Department of Biological Chemistry, School of Medicine, Molecular and Cellular Biology Laboratory, Institutes of Biomedical Sciences, Department of Biology, School of Life Science, Fudan University, Shanghai 200032, China
    Mol Cell Biol 28:2426-36. 2008
    ..Our results elucidate a molecular mechanism for TAZ regulation and indicate a potential function of TAZ as an important target of the Hippo pathway in regulating cell proliferation tumorigenesis...
  2. ncbi The N-terminal phosphodegron targets TAZ/WWTR1 protein for SCFβ-TrCP-dependent degradation in response to phosphatidylinositol 3-kinase inhibition
    Wei Huang
    Key Laboratory of Molecular Medicine, Ministry of Education, Department of Biochemistry and Molecular Biology, Shanghai Medical College, Fudan University, Shanghai 200032, China
    J Biol Chem 287:26245-53. 2012
    ..This study provides a novel mechanism of TAZ regulation and suggests a role of TAZ in modulating tissue growth and tumor development in response to PI3K signaling...
  3. ncbi TEAD transcription factors mediate the function of TAZ in cell growth and epithelial-mesenchymal transition
    Heng Zhang
    Molecular and Cell Biology Laboratory, Institutes of Biomedical Sciences, School of Life Science, Fudan University, Shanghai, China 200032
    J Biol Chem 284:13355-62. 2009
    ..Our study establishes a functional partnership between TAZ and TEAD under negative regulation by the Hippo signaling pathway...
  4. ncbi PP1 cooperates with ASPP2 to dephosphorylate and activate TAZ
    Chen Ying Liu
    Key Laboratory of Molecular Medicine, Ministry of Education, Department of Biochemistry and Molecular Biology School of Medicine, Lab, Institutes of Biomedical Sciences, Fudan University, Shanghai 200032, China
    J Biol Chem 286:5558-66. 2011
    ..As a result, PP1 and ASPP2 increase TAZ-dependent gene expression. This study demonstrates that PP1A and ASPP2 play a critical role in promoting TAZ function by antagonizing the LATS kinase through TAZ dephosphorylation...
  5. ncbi Targeted polyubiquitylation of RASSF1C by the Mule and SCFβ-TrCP ligases in response to DNA damage
    Xin Zhou
    Key Laboratory of Molecular Medicine, Ministry of Education, Department of Biochemistry and Molecular Biology, Shanghai Medical College, Shanghai 200032, China
    Biochem J 441:227-36. 2012
    ..Thus the present study reveals a novel regulation of RASSF1C and the potentially important role of RASSF1C in DNA damage responses...
  6. ncbi The relationship between PTEN expression and anoikis in human lung carcinoma cell lines
    Qun Ying Lei
    Key Laboratory of Glycoconjugate Research, Ministry of Health, Biochemistry Department, Fudan University Medical College, Shanghai 200032, China
    Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai) 34:463-8. 2002
    ..PTEN decreased the phosphorylation level of PKB and down-regulated FAK expression in HLCC. These results suggest that PTEN expression is different in 8 HLCC lines, and PTEN was involved in anoikis...
  7. ncbi Acetylation targets the M2 isoform of pyruvate kinase for degradation through chaperone-mediated autophagy and promotes tumor growth
    Lei Lv
    Key Laboratory of Molecular Medicine, Ministry of Education, Department of Biochemistry and Molecular Biology, Fudan University, Shanghai 200032, China
    Mol Cell 42:719-30. 2011
    ..These results reveal an acetylation regulation of pyruvate kinase and the link between lysine acetylation and CMA...