Prof. Sheng-Xiang Lin
Laval University Medical Center, Quebec, Canada.
Email: [email protected]
Qualifications
1982-1984 Doctorat d'État Institut de Biologie Moléculaire et Cellulaire: Strasbourg, Alsace, FR
1979-1982 Ph. D Institut de Biologie Moléculaire et Cellulaire: Strasbourg, Alsace, France
1979 M. Sc. Institute of Biochemistry and Cell Biology: Shanghai, Shanghai, China
Publications
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Wang, R., Wang, X., Su, P., et al. (2026). Developing Potential Endocrine Therapy Controlling Estradiol and DHT by Targeting 17β-HSD7 Against ER plus Breast Cancer. Cells, 15(15), Article 1345.
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Sancéau, J.-Y., Maltais, R., Zhou, M., et al. (2024). Synthesis and characterization of targeted 17β-hydroxysteroid dehydrogenase type 7 inhibitors. The Journal of Steroid Biochemistry and Molecular Biology, 242, Article 106544.
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Iqbal, S., & Lin, S.-X. (2023). Deep Drug Discovery of Mac Domain of SARS-CoV-2 (WT) Spike Inhibitors: Using Experimental ACE2 Inhibition TR-FRET Assay, Screening, Molecular Dynamic Simulations and Free Energy Calculations. Bioengineering, 10(8), Article 961.
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Zhang, W., & Lin, S.-X. (2023). Search of Novel Small Molecule Inhibitors for the Main Protease of SARS-CoV-2. Viruses, 15(2), Article 580.
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Li, T., Song, X., Stephen, P., et al. (2023). New insights into the substrate inhibition of human 17ss-hydroxysteroid dehydrogenase type 1. The Journal of Steroid Biochemistry and Molecular Biology, 228, Article 106246.
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Sang, X., Belmessabih, N., Wang, R., et al. (2022). CRIF1-CDK2 Interface Inhibitors Enhance Taxol Inhibition of the Lethal Triple-Negative Breast Cancer. Cancers, 14(4), Article 989.
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Thériault, J.-F., Poirier, D., & Lin, S.-X. (2021). The multi-specific human 17 beta-hydroxysteroid dehydrogenase type 7: Non-competitive inhibitors can target different catalyses to facilitate breast cancer treatment. The Journal of Steroid Biochemistry and Molecular Biology, 214, Article 105963.
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Wang, R., Stephen, P., Tao, Y., et al. (2021). Human endeavor for anti-SARS-CoV-2 pharmacotherapy: A major strategy to fight the pandemic. Biomedicine & Pharmacotherapy, 137, Article 111232.
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Wang, R., Li, T., Li, G., et al. (2021). An unprecedented endocrine target for ovarian cancer: inhibiting 17β-HSD7 supresses cancer cell proliferation and arrests G2/M cycle. American Journal of Cancer Research, 11(11), 5358–5367.
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Audet-Walsh, É., Wang, X. Q., & Lin, S.-X. (2020). Using Omics to better understand steroid biosynthesis, metabolism, and functions. The Journal of Steroid Biochemistry and Molecular Biology, 202, Article 105686.
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Zhang, W.-F., Stephen, P., Thériault, J.-F., et al. (2020). Novel Coronavirus Polymerase and Nucleotidyl-Transferase Structures: Potential to Target New Outbreaks. The Journal of Physical Chemistry Letters, 11(11), 4430–4435.
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Zhang, W.-F., Li, T., & Lin, S.-X. (2020). Meta-Analysis of steroid-converting enzymes and related receptors in prostate cancer suggesting novel combined therapies. The Journal of Steroid Biochemistry and Molecular Biology, 198, Article 105559.
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Li, T., Zhang, W., & Lin, S.-X. (2020). Steroid enzyme and receptor expression and regulations in breast tumor samples - A statistical evaluation of public data. The Journal of Steroid Biochemistry and Molecular Biology, 196, Article 105494.
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Zhang, C.-Y., Calvo, E.-L., Yang, C.-Q., et al. (2019). Transcriptome of 17β-hydroxysteroid dehydrogenase type 2 plays both hormone-dependent and hormone-independent roles in MCF-7 breast cancer cells. The Journal of Steroid Biochemistry and Molecular Biology, 195, Article 105471.
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Liu, W.-J., Zhao, G., Zhang, C.-Y., et al. (2020). Comparison of the roles of estrogens and androgens in breast cancer and prostate cancer. Journal of Cellular Biochemistry, 121(4), 2756–2769.
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Sang, X., Han, H., Li, T., et al. (2019). Mutual regulations and breast cancer cell control by steroidogenic enzymes: Dual sex-hormone receptor modulation upon 17β-HSD7 inhibition. The Journal of Steroid Biochemistry and Molecular Biology, 193, Article 105411.
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Li, T., Stephen, P., Zhu, D.-W., et al. (2019). Crystal structures of human 17β-hydroxysteroid dehydrogenase type 1 complexed with estrone and NADP+ reveal the mechanism of substrate inhibition. The FEBS Journal, 286(11), 2155–2166.
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Tchernof, A., Lin, S. X., Van, L. T., et al. (2019). The Passing of Dr. Fernand Labrie (1937-2019): The legacy of excellence in science Obituary. The Journal of Steroid Biochemistry and Molecular Biology, 189, 63–64.
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Thériault, J.-F., & Lin, S.-X. (2019). The dual sex hormone specificity for human reductive 17β-hydroxysteroid dehydrogenase type 7: Synergistic function in estrogen and androgen control. The Journal of Steroid Biochemistry and Molecular Biology, 186, 61–65.
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Ran, Q., Xiang, Y., Stephen, P., et al. (2019). CRIF1-CDK2 Interface Inhibitors: An Unprecedented Strategy for Modulation of Cell Radiosensitivity. Journal of the American Chemical Society, 141(4), 1420–1424.
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Li, F., Zhu, Z., Xue, M., et al. (2019). siRNA-based breast cancer therapy by suppressing 17β-hydroxysteroid dehydrogenase type I in an optimized xenograft cell and molecular biology model in vivo. Drug Design, Development and Therapy, 13, 757–766.
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Sang, X., Han, H., Poirier, D., et al. (2018). Steroid sulfatase inhibition success and limitation in breast cancer clinical assays: An underlying mechanism. The Journal of Steroid Biochemistry and Molecular Biology, 183, 80–93.
Profile Details
https://www.crchudequebec.ulaval.ca/en/researcher/sheng-xiang-lin/
https://scholar.google.com/citations?user=F7ZJctkAAAAJ&hl=fr
https://www.researchgate.net/scientific-contributions/Shengxiang-Lin-2107122335
WOS ResearcherID: JUR-8551-2023