施柏漳 助理教授
研究領域:蛋白質降解藥物開發、靶向蛋白降解、藥物化學
最高學歷:英國倫敦大學學院藥學院 博士
E-mail:po-chang.shih.23@mail.nsysu.edu.tw
連絡電話:07-5252000 #7207
辦公室:IR6001
個人網頁:https://sites.google.com/view/shih-lab/home
學經歷 | ||||||||||||||||
國立中山大學醫學院生技醫藥研究所助理教授 | 2023/8-至今 | |||||||||||||||
美東京大學/日本學術振興會 JSPS 研究員 | 2022/04-2023/06 | |||||||||||||||
高雄長庚醫院 博士後研究人員 | 2021/09-2022/04 | |||||||||||||||
心悅生醫股份有限公司 | 2020/02-2021/08 | |||||||||||||||
英國倫敦大學學院藥學院 博士 | ||||||||||||||||
專業 | ||||||||||||||||
小分子藥物開發、蛋白質降解藥物開發、藥物化學、靶像蛋白降解 | ||||||||||||||||
學術榮譽 | ||||||||||||||||
國立中山大學新進教師獎勵 | 2023-2024 | |||||||||||||||
JSPS Postdoctoral Fellowship (Standard) | ||||||||||||||||
台灣科技部博士創新計畫 | ||||||||||||||||
UCL School of Pharmacy Best PhD Student Publication Award 2018, UK | ||||||||||||||||
Poster Prize at 10th BMCS Biological and Medicinal Chemistry Postgraduate Symposium, UK | ||||||||||||||||
中華民國斐陶斐榮譽會員 | ||||||||||||||||
講授科目 | ||||||||||||||||
• 毒理學 | ||||||||||||||||
• 藥物代謝與藥物動力學 | ||||||||||||||||
• 蛋白質降解藥物開發特論 (一) | ||||||||||||||||
• 蛋白質降解藥物開發特論 (二) | ||||||||||||||||
• 雙功能分子藥物開發專題研究(一) | ||||||||||||||||
• 雙功能分子藥物開發專題研究(二) | ||||||||||||||||
專利及專書 | ||||||||||||||||
Chih-Hung Lin, Po-Chang Shih, Guochuan Emil Tsai. Perspective Chapter-NMDA Treatments for CNS Disorders (2021) IntechOpen | ||||||||||||||||
期刊論文 | ||||||||||||||||
• Wen, Z.-H., Chang, L., Yang, S.-N., Yu, C,-L., Tung, F.-Y., Kuo, H.-M., Lu, I.-C,. Wu, C.-Y.,Shih, P.-C., Chen, W.-F, Chen, N.-F. The anti-angiogenic and anti-vasculogenic mimicry effects of GN25 in endothelial and glioma cells. Biochimica et Biophysica Acta (BBA)-Molecular Cell Research. 2024. https://doi.org/10.1016/j.bbamcr.2024.119799 (IF: 4.6, 74/313= 23.6% in Biochemistry & Molecular Biology) | ||||||||||||||||
• Chiang, Y.-C., Selvam P, Liu, Y.-X., Shih, P.-C., Chen, N.-F., Kuo, H.-M., Lin, H.-Y., Wen, Z.-H., Chen, W.-F. STAT3 phosphorylation inhibitor Bt354 exhibits anti-neoplastic activity in glioblastoma multiforme cells. Environmental Toxicology. 2024. https://doi.org/10.1002/tox.24178 (IF: 4.5, 16/94= 17.0% in Toxicology) | ||||||||||||||||
• Shih, P.-C., Naganuma, M., Tsuji G., Demizu, Y., Naito, M. Development of decoy oligonucleotide-warheaded chimeric molecules targeting STAT3. Bioorganic and Medicinal Chemistry. 2023. https://doi.org/10.1016/j.bmc.2023.117507 (IF: 3.5, 12/52 = 23.1% in Organic Chemistry) | ||||||||||||||||
• Shih, P.-C., Naganuma, M., Demizu, Y., Naito, M. Current status of oligonucleotide-based protein degraders. Pharmaceutics. 2023. https://doi.org/10.3390/pharmaceutics15030765 (IF: 5.4, 51/277= 18.2% in Pharmacology & Pharmacy) | ||||||||||||||||
• Wen, Z.-H.*, Kuo, H.-M.*, Shih, P.-C.*, Hsu, L.-C., Chuang, J. M.-J., Chen, N.-F., Sun, H.-W., Liu, H.-T., Sung, C.-S., Chen, W.-F. Isoaaptamine increases ROS levels causing autophagy and mitochondria-mediated apoptosis in glioblastoma multiforme cells. Biomedicine & Pharmacotherapy. 2023 https://doi.org/10.1016/j.biopha.2023.114359 (IF: 7.5, 23/277= 8.1% in Pharmacology & Pharmacy) *The authors contributed equally. |
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• Mao, Y.-W., Lu, L.-P., Shih, P.-C., Hsiao, J.-F., Wu, V., Tsai, G. E. Ultrapure and potent tannic acid (UPPTA) is a novel inhibitor of D-amino acid oxidase to improve the N-methyl-D-aspartate function of CNS disorders. Phytomedicine | ||||||||||||||||
• Hsu S.-Y., Wen, Z.-H., Shih, P.-C., Kuo, H.-M., Lin, S.-C., Liu, H.-T., Lee, Y.-H., Wang, Y.-J., Chen, W.-F., Chen, N.-F. Sinularin Induces Oxidative Stress-Mediated Apoptosis and Mitochondrial Dysfunction, and Inhibits Angiogenesis in Glioblastoma Cells. Antioxidants. 2022; https://doi.org/10.3390/antiox11081433 (IF: 7.0, 6/60 = 10% in Chemistry, Medicinal) | ||||||||||||||||
• Kuo, T.-J., Jean, Y.-H., Shih, P.-C., Cheng, S.-Y., Kuo, H.-M., Lee, Y.-T., Lai, Y.-C., Tseng, C.-C., Chen, W.-F., and Wen, Z.-H. Stellettin B Induces Autophagic Cell Death and Apoptosis through Endoplasmic Reticulum in Human Oral Cancer. International Journal of Molecular Sciences. 2022; https://doi.org/10.3390/ijms23158813 (IF: 5.6, 66/285 = 23% in Biochemistry & Molecular Biology) | ||||||||||||||||
• Shih, P.-C.*, Mao, Y.-W.*, Hu, J.-W.*, Hsieh, H.-Y.*, Shih, T.-M.*, Lu, L.-P.*, Chang, W.-H.*, Huang, C.-H.*, Lin, C.-H.*, Lin, C.-H., Tan, P., Yang, Y.-C., Chien, M.-H., Su, C.-C., Ye, C.-H., Chuang, P.-Y., Hsieh, T.-L., Wang, C.-C., Hsieh, P.-S., Chou, T.-Y., Tsai, G. E. Development of the ultrapure and potent tannic acid as an orally bioavailable, pancoronal antiviral therapeutic. ACS Pharmacology & Translational Science. 2022; https://doi.org/10.1021/acsptsci.1c00264 (IF: 6.0, 25/366=6.8% in Pharmacology & Pharmacy) (被選為期刊封面、臨床試驗NCT04911777的臨床前數據發表) *The authors contributed equally. |
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• Shih, P.-C.# The role of the STAT3 signaling transduction pathways in radioresistance. Pharmacology & Therapeutics. 2022; https://doi.org/10.1016/j.pharmthera.2022.108118 (IF: 13.5, 7/277=2.3% in Pharmacology & Pharmacy) #First author and corresponding author. |
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• Chen, Y.-P.*, Shih, P.-C.*, Feng, C.-W., Wu, C.-C., Tsui, K.-H., Lin, Y.-H., Kuo, H.-M., and Wen, Z.-H. Pardaxin activates excessive mitophagy and mitochondria-mediated apoptosis in human ovarian cancer by inducing reactive oxygen species. Antioxidants. 2021; https://doi.org/10.3390/antiox10121883 (IF: 7.0, 6/60 = 10% in Chemistry, Medicinal) *The authors contributed equally. |
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• Lin, C.-H., Shih, P.-C., Tsai, G. E. Perspective Chapter: NMDA Treatments for CNS Disorders under the book title Ketamine Revisited - New Insights into NMDA Inhibitors. IntechOpen. 2021 | ||||||||||||||||
• Ko, C.-Y.*, Shih, P.-C.*, Huang, P.-W., Lee, Y.-H., Chen, Y.-F., Tai M.-H., Liu, C.-H., Wen, Z.-H., Kuo, H.-M. Sinularin, an anti-cancer agent causing mitochondria-modulated apoptosis and cytoskeleton disruption in human hepatocellular carcinoma. International Journal of Molecular Sciences.2021; https://doi.org/10.3390/ijms22083946 (IF: 5.6, 66/285 = 23% in Biochemistry & Molecular Biology) *The authors contributed equally. |
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• Shih, P.-C.#, Mei, K.-C. Role of STAT3 signaling transduction pathways in cancer stem cell-associated chemoresistance. Drug Discovery Today.2021; https://doi.org/10.1016/j.drudis.2020.11.032 (IF: 7.4, 24/277= 8.5 % in Pharmacology & Pharmacy) #First author and corresponding author. |
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• Yuan, C.-H.*, Ma, Y.-L.*, Shih, P.-C.*, Chen, C.-T., Cheng, S.-Y., Pan, C.-Y., Jean, Y.-H., Chu, Y.-M., Lin, S.-C, Lai, Y,-C., Kuo, H,-M. The antimicrobial peptide tilapia piscidin 3 induces mitochondria-modulated intrinsic apoptosis of osteosarcoma cells. Biochemical Pharmacology. 2020;. doi: 10.1016/j.bcp.2020.114064 (IF: 5.8, 40/277 = 14.3% in Pharmacology & Pharmacy) *The authors contributed equally. |
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• Chen, Y.-F.*, Shih, P.-C.*, Kuo, H.-M.*, Yang, S.-N., Lin, Y.-Y., Chen, W.-F., Tzou, S.-J., Liu, H.-T., Chen, N.-F. TP3, an antimicrobial peptide, inhibits infiltration and motility of glioblastoma cells via modulating the tumor microenvironment. Cancer Medicine. 2020;. doi: 10.1002/cam4.3005 (IF: 4.0, 96/241 = 39.6% in Oncology) *The authors contributed equally. |
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• Shih, P.-C.# Revisiting the development of small molecular inhibitors that directly target the signal transducer and activator of transcription 3 (STAT3) domains. Life Sciences. 2019; doi: 10.1016/j.lfs.2019.117241 (IF: 6.1, 35/277 = 12.5% in Pharmacology & Pharmacy) #First author and corresponding author. |
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• Shih, P.-C., Yang, Y., Parkinson, G. N., Wilderspin, A. & Wells, G. A high-throughput fluorescence polarization assay for discovering inhibitors targeting the DNA-binding domain of signal transducer and activator of transcription 3 (STAT3). Oncotarget. 2018; doi: 10.18632/oncotarget.26013 | ||||||||||||||||
研究計畫、國科會計畫、產學合作計畫 | ||||||||||||||||
國科會計畫 | ||||||||||||||||
112 | 離體發展高安全性、有效性並具臨床潛力的新穎STAT3蛋白質降解藥物 | |||||||||||||||
113-115 | 以新穎藥理機制離體開發抗神經性疼痛藥物 |
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