潘秀玲(Pan, Shiow-Lin) 教授

Email
slpan@tmu.edu.tw
現   職
癌症生物學與藥物研發研究所 教授
醫學科技學院 院長

學經歷

學 歷

畢業學校與學位[修業時間]
台大醫學院藥理學研究所 博士
1998/07~2002/06
台北醫學大學醫學研究所藥理組 碩士
1992/07~1994/06

本校學術經歷

任職單位與職稱[起迄時間]
癌症生物學與藥物研發研究所教授
2018/12/01~
癌症生物學與藥物研發博士學位學程教授
2016/02/01~2018/11/30
癌症生物學與藥物研發博士學位學程副教授
2013/02/01~2016/01/31

本校兼職教學行政經歷

服務單位與職稱[起迄時間]
醫學科技學院院長
2023/03/01 ~
醫學科技學院副院長
2020/08/01 ~ 2023/02/28
新藥研發產業博士學位學程主任
2020/08/01 ~ 2022/07/31
(舊)臨床藥物基因體學暨蛋白質體學碩士學位學程教授
2020/05/01 ~
(舊)生技醫療產業研發博士學位學程主任
2019/02/01 ~ 2020/07/31
癌症生物學與藥物研發博士學位學程教授
2019/01/01 ~
(舊)生技醫療產業研發博士學位學程教授
2017/06/01 ~
藥理學科
2014/08/01 ~

其它經歷

任職單位與職稱[起迄時間]
國家衛生研究院生技藥研所助研究員
2009/12~2013/01
台大醫學院客座助理研究員
2007/08~2009/12
台大醫學院特約博士後研究
2004/08~2007/07
台大醫學院博士後研究
2002/08~2004/07
長庚大學助教
1994/08~1998/07

專長與研究領域

學門領域
藥理及毒理
藥學
學術專長
動物模式

論文著作

清冊下載


1. 2024 Tu HJ,Chao MW,Lee CC,Peng CS,Wu YW,Lin TE, Chang YW, Yen SC, Hsu KC, Pan SL*, HuangFu WC*.. Discovering a novel dual specificity tyrosine-phosphorylation-regulated kinase 1A (DYRK1A) inhibitor and its impact on tau phosphorylation and amyloid-β formation. . J Enzyme Inhib Med Chem .2024 ;(39):2418470-2418477

2. 2024 Shih WH,Huang HL,HuangFu WC,Lin TE,Sung TY,Li MC, Huang GL, Chang YW, Yen SC, Hsieh HP, Hsu KC*, Pan SL*. Discovery of novel TANK-Binding Kinase 1 (TBK1) inhibitor against pancreatic ductal adenocarcinoma. . Int J Biol Macromol. .2024

3. 2024 Wu Yi Wen,HuangFu Wei Chun,Lin Tony Eight,Peng Chao Hsiang,Tu Huang Ju,Sung Ting Yi,Sung Tzu Ying,Yen Shih Chung,Pan Shiow Lin,Hsu Kai Cheng,Wu Yi Wen,HuangFu Wei Chun,Lin Tony Eight,Peng Chao Hsiang,Tu Huang Ju,Sung Ting Yi,Sung Tzu Ying,Yen Shih Chung,Pan Shiow Lin,Hsu Kai Cheng. Identification of selective dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) inhibitors and their effects on tau and microtubule . International Journal of Biological Macromolecules .2024 ;(259)

4. 2024 Huang Cheng Chiao,Hsu Chia Ming,Chao Min Wu,Hsu Kai Cheng,Lin Tony Eight,Yen Shih Chung,Tu Huang Ju,Pan Shiow Lin,Huang Cheng Chiao,Hsu Chia Ming,Chao Min Wu,Hsu Kai Cheng,Lin Tony Eight,Yen Shih Chung,Tu Huang Ju,Pan Shiow Lin. In silico identification of a novel Cdc2-like kinase 2 (CLK2) inhibitor in triple negative breast cancer . Protein Science .2024 ;(33)

5. 2023 Chang CD, Chao MW, Lee HY, Liu YT, Tu HJ, Lien ST, Lin TE, Sung TY, Yen SC, Huang SH, Hsu KC, Pan SL*. In silico identification and biological evaluation of a selective MAP4K4 inhibitor against pancreatic cancer. . J Enzyme Inhib Med Chem. .2023 ;(38):2166039-2166049

6. 2023 Tu HJ,Su CJ,Peng CS,Lin TE,HuangFu WC,Hsu KC, Hwang TL*, Pan SL*. Urolithin A exhibits a neuroprotective effect against Alzheimer's disease by inhibiting DYRK1A activity. . J Food Drug Anal. .2023

7. 2022 Lin TE, Chao MW, HuangFu WC, Tu HJ, Peng ZX, Su CJ, Sung TY, Hsieh JH, Lee CC, Yang CR, Pan SL, Hsu KC. Identification and analysis of a selective DYRK1A inhibitor. . Biomed Pharmacother. .2022

8. 2022 Yen SC, Chen LC, Huang HL, HuangFu WC, Chen YY, Eight Lin T, Lien ST, Tseng HJ, Sung TY, Hsieh JH, Huang WJ, Pan SL, Hsu KC. . Bioorg Chem. .2022

9. 2022 Yen SC, Wu YW, Huang CC, Chao MW, Tu HJ, Chen LC, Lin TE, Sung TY, Tseng HJ, Chu JC, Huang WJ, Yang CR, HuangFu WC, Pan SL*, Hsu KC*. O-methylated flavonol as a multi-kinase inhibitor of leukemogenic kinases exhibits a potential treatment for acute myeloid leukemia. . Phytomedicine .2022 ;(100):154061-154071

10. 2021 Yen SC,Chen LC,Huang HL,Ngo ST,Wu YW,Lin TE, Sung TY, Lien ST, Tseng HJ, Pan SL, Huang WJ, Hsu KC. Yen SC, Chen LC, Huang HL, Ngo ST, Wu YW, Lin TE, Sung TY, Lien ST, Tseng HJ, Pan SL, Huang WJ, Hsu KC. Investigation of Selected Flavonoid Derivatives as Potent FLT3 Inhibitors for the Potential Treatment of Acute Myeloid Leukemia. . J Nat Prod. .2021 ;(84):1-10

11. 2021 Sung TY,Huang HL,Cheng CC,Chang FL,Wei PL,Cheng YW, Huang CC*, Lee YC*, HuangFu WC*, Pan SL*. . Sung TY, Huang HL, Cheng CC, Chang FL, Wei PL, Cheng YW, Huang CC*, Lee YC*, HuangFu WC*, Pan SL*. EGFL6 promotes colorectal cancer cell growth and mobility and the anti-cancer property of anti-EGFL6 antibody. . Cell Biosci. .2021 ;(11):53-63

12. 2021 Liu YM,Tu HJ,Wu CH,Lai MJ,Yu SC,Chao MW, Wu YW, Teng CM, Pan SL*, Liou JP*. . Liu YM, Tu HJ, Wu CH, Lai MJ, Yu SC, Chao MW, Wu YW, Teng CM, Pan SL*, Liou JP*. Ring-opening of five-membered heterocycles conjugated 4-isopropylresorcinol scaffold-based benzamides as HSP90 inhibitors suppressing tumor growth in vitro and in vivo. . Eur J Med Chem. .2021 ;(219):113428-113438

13. 2021 Wu YW,Chao MW,Tu HJ,Chen LC,Hsu KC,Liou JP, Yang CR, Yen SC, HuangFu WC*, Pan SL*.. Wu YW, Chao MW, Tu HJ, Chen LC, Hsu KC, Liou JP, Yang CR, Yen SC, HuangFu WC*, Pan SL*. A novel dual HDAC and HSP90 inhibitor, MPT0G449, downregulates oncogenic pathways in human acute leukemia in vitro and in vivo. . Oncogenesis .2021 ;(10):39-50

14. 2021 Chang TY,Nepali K,Chen YY,Yang YSH,Hsu KC,Yen Y, Pan SL, Liou JP, Lee SB.. Chang TY, Nepali K, Chen YY, Yang YSH, Hsu KC, Yen Y, Pan SL, Liou JP, Lee SB. A novel histone deacetylase inhibitor MPT0L184 dysregulates cell-cycle checkpoints and initiates unscheduled mitotic signaling. . Biomed Pharmacother. .2021 ;(138):111485-111495

15. 2021 Chao MW,Lin TE,HuangFu WC,Chang CD,Tu HJ,Chen LC, Yen SC, Sung TY, Huang WJ, Yang CR, Pan SL, Hsu KC.. Chao MW, Lin TE, HuangFu WC, Chang CD, Tu HJ, Chen LC, Yen SC, Sung TY, Huang WJ, Yang CR, Pan SL, Hsu KC. Identification of a dual TAOK1 and MAP4K5 inhibitor using a structure-based virtual screening approach. . J Enzyme Inhib Med Chem .2021 ;(36):98-108

16. 2020 Mehndiratta S,Lin MH ,Wu YW,Chen CH,Wu TY ,Chuang KH, Chao MW, Chen YY, Pan SL, Chen MC, Liou JP. Mehndiratta S, Lin MH, Wu YW, Chen CH, Wu TY, Chuang KH, Chao MW, Chen YY, Pan SL, Chen MC, Liou JP*. Nanilide hydroxamates as dual inhibitors of HDAC and HSP90, downregulating IFN-γ induced PD-L1 expression. . Eur J Med Chem. .2020 ;(185):111725

17. 2020 Tseng HJ,Lin MH,Shiao YJ,Yang YC,Chu JC,Chen CY, Chen YY, Lin TE, Su CJ, Pan SL, Chen LC, Wang CY, Hsu KC, Huang WJ.. Tseng HJ, Lin MH, Shiao YJ, Yang YC, Chu JC, Chen CY, Chen YY, Lin TE, Su CJ, Pan SL, Chen LC, Wang CY, Hsu KC, Huang WJ*. Synthesis and biological evaluation of acridine-based histone deacetylase inhibitors as multitarget agents against Alzheimer's disease. . Eur J Med Chem. .2020 ;(192):112193

18. 2020 Ojha R,Nepali K,Chen CH,Chuang KH,Wu TY,Lin TE, Hsu KC, Chao MW, Lai MJ, Lin MH, Huang HL, Chang CD, Pan SL, Chen MC, Liou JP.. Ojha R, Nepali K, Chen CH, Chuang KH, Wu TY, Lin TE, Hsu KC, Chao MW, Lai MJ, Lin MH, Huang HL, Chang CD, Pan SL, Chen MC, Liou JP*. Isoindoline scaffold-based dual inhibitors of HDAC6 and HSP90 suppressing the growth of lung cancer in vitro and in vivo. . Eur J Med Chem. .2020 ;(190):112086

19. 2020 Lin CF,Hsu KC,HuangFu WC,Lin TE,Huang HL,Pan SL. Lin CF, Hsu KC, HuangFu WC, Lin TE, Huang HL*, Pan SL*. Investigating the potential effects of selective histone deacetylase 6 inhibitor ACY1215 on infarct size in rats with cardiac ischemia-reperfusion injury. . BMC Pharmacol Toxicol. .2020 ;(21):21

20. 2020 Chang FL,Tsai KC,Lin TY,Yang TW,Lo YN,Chen WC, Chang JH, Lu MK, Chiou CT, Chen PH, Yen Y*, Pan SL*, Lee YC*.. Chang FL, Tsai KC, Lin TY, Yang TW, Lo YN, Chen WC, Chang JH, Lu MK, Chiou CT, Chen PH, Yen Y*, Pan SL*, Lee YC*. Astragalus membranaceus-Derived Anti-Programmed Death-1 Monoclonal Antibodies with Immunomodulatory Therapeutic Effects against Tumors. . Biomed Res Int. .2020 ;(2020):3415471

21. 2020 Lee YC,Huang HT,Chang CD,Chen CT,Lin TY,Yang TW, Chang FL, Lu MK, Chiou CT, Chen WC, Pan SL, Tsai KC. Lee YC, Huang HT, Chang CD, Chen CT, Lin TY, Yang TW, Chang FL, Lu MK, Chiou CT, Chen WC, Pan SL, Tsai KC. Isolation of anti-VEGF monoclonal antibodies with neutralizing effects from an Astragalus-induced immune antibody library. . Int Immunopharmacol. .2020 ;(88):107007

22. 2020 Chen LC,Huang HL,HuangFu WC,Yen SC,Ngo ST,Wu YW, Lin TE, Sung TY, Lien ST, Tseng HJ, Pan SL, Huang WJ, Hsu KC.. Chen LC, Huang HL, HuangFu WC, Yen SC, Ngo ST, Wu YW, Lin TE, Sung TY, Lien ST, Tseng HJ, Pan SL, Huang WJ, Hsu KC. Biological Evaluation of Selected Flavonoids as Inhibitors of MNKs Targeting Acute Myeloid Leukemia. . J Nat Prod. .2020 ;(83):2967-2975

23. 2020 Wu WC,Liu YM,Liao YH,Hsu KC,Lien ST,Chen IC, Lai MJ, Li YH, Pan SL, Chen MC, Liou JP. . Wu WC, Liu YM, Liao YH, Hsu KC, Lien ST, Chen IC, Lai MJ, Li YH, Pan SL, Chen MC, Liou JP. Fluoropyrimidin-2,4-dihydroxy-5-isopropylbenzamides as antitumor agents against CRC and NSCLC cancer cells. . Eur J Med Chem. .2020 ;(203):112540-112550

24. 2020 Hsu KC,HuangFu WC,Lin TE,Chao MW,Sung TY,Chen YY, Pan SL, Lee JC, Tzou SC, Sun CM, Yang JM.. Hsu KC, HuangFu WC, Lin TE, Chao MW, Sung TY, Chen YY, Pan SL, Lee JC, Tzou SC, Sun CM, Yang JM. A site-moiety map and virtual screening approach for discovery of novel 5-LOX inhibitors. . Sci Rep. .2020 ;(10):10510-10520

25. 2019 Hsieh YL,Tu HJ,Pan SL,Liou JP,Yang CR. Anti-metastatic activity of MPT0G211, a novel HDAC6 inhibitor, in human breast cancer cells in vitro and in vivo. . Biochim Biophys Acta Mol Cell Res .2019 ;(1866):992-1003

26. 2019 MPT0G413, A Novel HDAC6-Selective Inhibitor, and Bortezomib Synergistically Exert Anti-tumor Activity in Multiple Myeloma Cells. . Front Oncol. .2019 ;(9):249-258

27. 2019 Lin CF, Su CJ, Liu JH, Chen ST, Huang HL*, Pan SL*. Potential effects of CXCL9 and CCL20 on cardiac fibrosis in patients with myocardial infarction. . J. Clin. Med. .2019 ;(8):E659-E668

28. 2019 Chao MW; Chang LH; Tu HJ; Chang CD; Lai MJ; Chen YY; Liou JP; Teng CM; Pan SL*. Combination treatment strategy for pancreatic cancer involving the novel HDAC inhibitor MPT0E028 with a MEK inhibitor beyond K-Ras status. . Clinical Epigenetics .2019 ;(11):85-94

29. 2019 Amide-tethered quinoline-resorcinol conjugates as a new class of HSP90 inhibitors suppressing the growth of prostate cancer cells. . Bioorg Chem. .2019 ;(91):103119-103128

30. 2019 Huang HL, Liu YM, Sung TY, Huang TC, Cheng YW, Liou JP*, Pan SL*. TIMP3 expression associates with prognosis in colorectal cancer and its novel arylsulfonamide inducer, MPT0B390, inhibits tumor growth, metastasis and angiogenesis. . Theranostics .2019 ;(9):6676-6689

31. 2018 Lin SY,Yeh TK,Song JS,Hung MS,Cheng MF,Liao FY, Li AS, Cheng SY, Lin LM, Chiu CH, Wu MH, Lin YJ, Hsiao W, Sun M, Wang YH, Huang CH, Tang YC, Chang HH, Huang ZT, Chao YS, Shih C, Pan SL, Wu SY, Kuo CC, Ueng SH. . 4-Bromophenylhydrazinyl benzenesulfonylphenylureas as indoleamine 2,3-dioxygenase inhibitors with in vivo target inhibition and anti-tumor efficacy. . Bioorg Chem. .2018 ;(77):600-607

32. 2018 Ojha R,Huang HL,HuangFu WC,Wu YW,Nepali K,Lai MJ, Su CJ, Sung TY, Chen YL, Pan SL, Liou JP.. 1-Aroylindoline-hydroxamic acids as anticancer agents, inhibitors of HSP90 and HDAC. . Eur J Med Chem. .2018 ;(150):667-677

33. 2018 Wu YW,Hsu KC,Lee HY,Huang TC,Lin TE,Chen YL, Sung TY, Liou JP, Hwang-Verslues WW, Pan SL, HuangFu WC.. A Novel Dual HDAC6 and Tubulin Inhibitor, MPT0B451, Displays Anti-tumor Ability in Human Cancer Cells in Vitro and in Vivo. . Front Pharmacol. .2018 ;(9):205-210

34. 2018 A Novel Selective JAK2 Inhibitor Identified Using Pharmacological Interactions. . Front Pharmacol. .2018 ;(9):1379-1386

35. 2018 The anticancer effects of MPT0G211, a novel HDAC6 inhibitor, combined with chemotherapeutic agents in human acute leukemia cells. . Clin Epigenetics. .2018 ;(10):162-170

36. 2017 Liu YM,HuangFu WC,Huang HL,Wu WC,Chen YL,Yen Y, Huang HL, Nien CY, Lai MJ, Pan SL*, Liou JP.. 1,4-Naphthoquinones as inhibitors of Itch, a HECT domain-E3 ligase, and tumor growth suppressors in multiple myeloma. . Eur J Med Chem .2017 ;(140):84-91

37. 2017 Chang HY,Ye SP,Pan SL ,Kuo TT,Liu BC,Chen YL, Huang TC. Overexpression of miR-194 Reverses HMGA2-driven Signatures in Colorectal Cancer. . Theranostics .2017 ;(7):3889-3900

38. 2017 Chen MC,Kuo YC,Hsu CM,Chen YL,Shen CC,Teng CM, Pan SL*. The apoptotic mechanisms of MT-6, a mitotic arrest inducer, in human ovarian cancer cells. . Sci Rep. .2017 ;(7):46149-46161

39. 2017 Chao MW,Chen TH,Huang HL,Chang YW,HuangFu WC,Lee YC, Teng CM, Pan SL*. Lanatoside C, a cardiac glycoside, acts through protein kinase Cδ to cause apoptosis of human hepatocellular carcinoma cells. . Sci Rep. .2017 ;(7):46134-46145

40. 2017 Mehndiratta S,Wang RS,Huang HL,Su CJ,Hsu CM,Wu YW, Pan SL, Liou JP. 4-Indolyl-N-hydroxyphenylacrylamides as potent HDAC class I and IIB inhibitors in vitro and in vivo. . Eur J Med Chem .2017 ;(134):13-23

41. 2016 Mehndiratta S,Pan SL,Kumar S,Liou JP. Indole-3-ethylsulfamoylphenylacrylamides with Potent Anti-proliferative and Anti-angiogenic Activities. . Anticancer Agents Med Chem. .2016 ;(16):907-913

42. 2016 Lin SY,Yeh TK,Kuo CC,Song JS,Cheng MF,Liao FY, Chao MW, Huang HL, Chen YL, Yang CY, Wu MH, Hsieh CL, Hsiao W,... Pan SL, Hung MS, Ueng SH.. Phenyl benzenesulfonylhydrazides exhibit selective indoleamine 2,3-dioxygenase inhibition with potent in vivo pharmacodynamic activity and antitumor efficacy. . J Med Chem. .2016 ;(59):419-430

43. 2016 Chen CH,Liu YM,Pan SL,Liu YR,Liou JP,Yen Y. Trichlorobenzene-substituted azaaryl compounds as novel FGFR inhibitors exhibiting potent antitumor activity in bladder cancer cells in vitro and in vivo. . Oncotarget .2016 ;(7):26374-26387

44. 2016 Huang HL,Chao MW,Chen CC,Cheng CC,Chen MC,Lin CF, Liou JP, Teng CM, Pan SL. LTP-1, a novel antimitotic agent and Stat3 inhibitor, inhibits human pancreatic carcinomas in vitro and in vivo. . Sci Rep. .2016 ;(6):27794

45. 2016 Lin CF,Huang HL,Peng CY,Lee YC,Wang HP,Teng CM, Pan SL*. TW-01, piperazinedione-derived compound, inhibits ras-mediated cell proliferation and angioplasty-induced vascular restenosis. . Toxicol Appl Pharmacol .2016 ;(305):194-202

46. 2016 Huang HL,Chao MW,Li YC,Chang LH,Chen CH,Chen MC, Cheng CC, Liou JP, Teng CM, Pan SL*. MPT0G066, a novel anti-mitotic drug, induces JNK-independent mitotic arrest, JNK-mediated apoptosis, and potentiates antineoplastic effect of cisplatin in ovarian cancer . Sci Rep .2016 ;(6):31664-31672

47. 2016 Wang HY,Chang YL,Cheng CC,Chao MW,Lin SI,Pan SL, Hsu CC, Liu TW, Cheng HC, Tseng CP, Liu SJ, Tsai HJ, Chang HY, Hsu TA. Glucocorticoids may compromise the effect of gefitinib in non-small cell lung cancer . Oncotarget .2016 ;(7):85917-85928

48. 2015 Chen CH,Lee CH,Liou JP,Teng CM,Pan SL. Molecular mechanisms underlying the antitumor activity of (E)-N-hydroxy-3-(1-(4-methoxyphenylsulfonyl)-1,2,3,4-tetrahydroquinolin-6-yl)acrylamide in human colorectal cancer cells in vitro and in vivo. . Oncotarget. .2015 ;(6):35991-36002

49. 2015 Huang HL,Peng CY,Lai MJ,Chen CH,Lee HY,Wang JC, Liou JP, Pan SL, Teng CM.. Novel oral histone deacetylase inhibitor, MPT0E028, displays potent growth-inhibitory activity against human B-cell lymphoma in vitro and in vivo. . Oncotarget .2015 ;(6):4976-4991

50. 2015 Liu YM,Lee HY,Chen CH,Lee CH,Wang LT,Pan SL, Lai MJ, Yeh TK, Liou JP.. 1-Arylsulfonyl-5-(N-hydroxyacrylamide)tetrahydroquinolines as potent histone deacetylase inhibitors suppressing the growth of prostate cancer cells. . Eur J Med Chem. .2015 ;(89):320-330

51. 2015 Pai HC,Kumar S,Shen CC,Liou JP,Pan SL,Teng CM. MT-4 Suppresses Resistant Ovarian Cancer Growth through Targeting Tubulin and HSP27 . PLoS One .2015 ;(10):e01238

52. 2015 Tzeng HE,Yang L,Chen K,Wang Y,Liu YR,Pan SL, Gaur S, Hu S, Yen Y.. The pan-PI3K inhibitor GDC-0941 activates canonical WNT signaling to confer resistance in TNBC cells: resistance reversal with WNT inhibitor. . Oncotarget .2015 ;(6):11061-11073

53. 2015 Szu-Ying Wu,Ping-Jyun Sung,Ya-Ling Chang,Shiow-Lin Pan,Che-Ming Teng. Heteronemin, a Spongean Sesterterpene, Induces Cell Apoptosis, and Autophagy in Human Renal Carcinoma Cells . BioMed Research International (formerly titled Journal of Biomedicine and Biotechnology) .2015 ;(2015):738241-738253

54. 2015 Chao MW,Lai MJ,Liou JP,Chang YL,Wang JC,Pan SL, Teng CM.. The synergic effect of vincristine and vorinostat in leukemia in vitro and in vivo. . J Hematol Oncol. .2015 ;(8):82

55. 2015 Chao MW,Wang LT,Lai CY,Yang XM,Cheng YW,Lee KH, Pan SL, Teng CM.. eIF4E binding protein 1 expression is associated with clinical survival outcomes in colorectal cancer. . Oncotarget .2015 ;(6):24092-24107

56. 2015 Lai MJ,Lee HY,Chuang HY,Chang LH,Tsai AC,Chen MC, Huang HL, Wu YW, Teng CM, Pan SL, Liu YM, Mehndiratta S, Liou JP.. N-Sulfonyl-aminobiaryls as Antitubulin Agents and Inhibitors of Signal Transducers and Activators of Transcription 3 (STAT3) Signaling. . J Med Chem .2015 ;(58):6549-6558

57. 2015 Liu YM,Lee HY,Lai MJ,Pan SL,Huang HL,Kuo FC, Chen MC, Liou JP.. Pyrimidinedione-mediated selective histone deacetylase 6 inhibitors with antitumor activity in colorectal cancer HCT116 cells. . Org Biomol Chem. .2015 ;(13):10226-10235

58. 2014 Chen CH,Chen MC,Wang JC,Tsai AC,Chen CS,Liou JP*, Pan SL*, Teng CM*. Synergistic interaction between the HDAC inhibitor, MPT0E028, and sorafenib in liver cancer cells in vitro and in vivo. . Clin Cancer Res .2014 ;(20):1274-1287

59. 2014 Hsu JL,Lee YJ,Leu WJ,Dong YS,Pan SL,Uang BJ, Guh JH.. Moniliformediquinone induces in vitro and in vivo antitumor activity through glutathione-involved DNA damage response and mitochondrial stress in human hormone-refractory prostate cancers. . J Urol. .2014 ;(191):1429-1438

60. 2014 Tsai AC,Wang CY,Liou JP,Pai HC,Hsiao CJ,Chang JY, Wang JC, Teng CM, Pan SL*. Orally active microtubule-targeting agent, MPT0B271, for the treatment of human non-small cell lung cancer, alone and in combination with erlotinib. . Cell Death Dis. .2014 ;(5):e1162

61. 2014 Lee HY,Tsai AC,Chen MC,Shen PJ,Cheng YC,Kuo CC, Pan SL, Liu YM, Liu JF, Yeh TK, Wang JC, Chang CY, Chang JY, Liou JP. Azaindolylsulfonamides, with a More Selective Inhibitory Effect on Histone Deacetylase 6 Activity, Exhibit Antitumor Activity in Colorectal Cancer HCT116 Cells. . J Med Chem .2014 ;(57):4009-4022

62. 2014 Yu CC,Pan SL,Chao SW,Liu SP,Hsu JL,Yang YC, Li TK, Huang WJ, Guh JH.. A novel small molecule hybrid of vorinostat and DACA displays anticancer activity against human hormone-refractory metastatic prostate cancer through dual inhibition of histone deacetylase and topoisomerase I. . Biochem Pharmacol. .2014 ;(90):320-330

63. 2014 Wang MJ,Liu YQ,Chang LC,Wang CY,Zhao YL,Zhao XB, Qian K, Nan X, Yang L, Yang XM, Hung HY, Yang JS, Kuo DH, Goto M, Morris-Natschke SL, Pan S. Design, Synthesis, Mechanisms of Action, and Toxicity of Novel 20(S)-Sulfonylamidine Derivatives of Camptothecin as Potent Antitumor Agents. . J Med Chem. .2014 ;(57):6008-18

64. 2014 Wang LT,Liou JP,Li YH,Liu YM,Pan SL*,Teng CM*. A novel class I HDAC inhibitor, MPT0G030, induces cell apoptosis and differentiation in human colorectal cancer cells via HDAC1/PKCδ and E-cadherin. . Oncotarget. .2014 ;(5):5651-62

65. 2014 Wang CY,Liou JP,Tsai AC,Lai MJ,Liu YM,Lee HY, Wang JC, Pan SL*, Teng CM*. A novel action mechanism for MPT0G013, a derivative of arylsulfonamide, inhibits tumor angiogenesis through up-regulaiton of TIMP3 expression. . Oncotarget .2014 ;(5):9838-9850

66. 2014 Tsai AC,Pai HC,Wang CY,Liou JP,Teng CM,Wang JC, Pan SL. In vitro and in vivo antitumor effects of MPT0B014, a novel derivative aroylquinoline, and in combination with erlotinib in human non-small-cell lung cancer cells . British Journal of Pharmacology .2014 ;(171):122-133

67. 2013 Lee HY,Pan SL,Su MC,Liu YM,Kuo CC,Chang YT, Wu JS, Nien CY, Mehndiratta S, Chang CY, Wu SY, Lai MJ, and Liou JP. Furanylazaindoles: Potent Anticancer Agents in Vitro and in Vivo. . J Med Chem .2013 ;(56):8008-8018

68. 2013 Chen MC,Chen CH,Liu YN,Wang HP,Pan SL,Teng CM. TW01001, a novel piperazinedione compound, induces mitotic arrest and autophagy in non-small cell lung cancer A549 cells. . Cancer Lett. .2013 ;(336):370-378

69. 2013 Lai CY,Pan SL,Yang XM,Chang LH,Chang YL,Yang PC, Lee KH, Teng CM.. Depletion of 4E-BP1 and regulation of autophagy lead to YXM110-induced anti-cancer effects. . Carcinogenesis .2013 ;(34):2050-2060

70. 2013 Chang LH,Pan SL,Lai CY,Tsai AC,Teng CM. Activated PAR-2 Regulates Pancreatic Cancer Progression through ILK/HIF-α-Induced TGF-α Expression and MEK/VEGF-A-Mediated Angiogenesis. . Am J Pathol .2013 ;(183):566-575

71. 2013 Chen MC,Chen CH,Wang JC,Tsai AC,Liou JP,Pan SL, Teng CM. The HDAC inhibitor, MPT0E028, enhances erlotinib-induced cell death in EGFR-TKI-resistant NSCLC cells. . Cell Death Dis .2013 ;(4):e810

72. 2012 Pai HC,Chang LH,Peng CY,Chang YL,Chen CC,「Shen CC, Teng CM, Pan SL」. Moscatilin inhibits migration and metastasis of human breast cancer MDA-MB-231 cells through inhibition of Akt and Twist signaling pathway . J Mol Med .2012

73. 2012 Wang LT,Pan SL,Chen TH,Dong YZ,Lee KH,「Teng CM」. DYZ-2-90, a Novel Neo-tanshinlactone Ring-Opened Compound, Induces ERK-Mediated Mitotic Arrest and Subsequent Apoptosis by Activating JNK in Human Colorectal Cancer Cells . Chembiochem .2012 ;(13):1663-1672

74. 2012 Huang HL,Lee HY,Tsai AC,Peng CY,Lai MJ,「Wang JC, Pan SL, Teng CM, Liou JP」. Anticancer Activity of MPT0E028, a Novel Potent Histone Deacetylase Inhibitor, in Human Colorectal CancerHCT116 Cells In Vitro and In Vivo . PLoS One .2012 ;(7):e43645-e43656

75. 2012 Chao MW,Chen CH,Chang YL,Teng CM,Pan SL. α-Tomatine-mediated anti-cancer activity in vitro and in vivo through cell cycle- and caspase-independent pathways. . PLoS One .2012 ;(7):e44093-e44093

76. 2012 Lai CY,Tsai AC,Chen MC,Chang LH,Sun HL,Chang YL, Chen CC, Teng CM, Pan SL. Aciculatin Induces p53-dependent apoptosis via MDM2 depletion in human cancer cells in vitro and in vivo. . PLoS One .2012 ;(7):e42192-e42192

77. 2012 Yang X,Shi Q,Lai CY,Chen CY,Ohkoshi E,Yang SC,Wang CY, Bastow KF, Wu TS, Pan SL, Teng CM, Yang PC, Lee KH. Antitumor agents 295. E-ring hydroxylated antofine and cryptopleurine analogues as antiproliferative agents: design, synthesis, and mechanistic studies. . J Med Chem .2012 ;(55):6751-61

78. 2012 Wu SY,Leu YL,Chang YL,Wu TS,Kuo PC,Liao YR, Teng CM, Pan SL. Physalin F induces cell apoptosis in human renal carcinoma cells by targeting NF-kappaB and generating reactive oxygen species. . PLoS One .2012 ;(7):e40727-e40727

79. 2012 Lo HM,Wu MW,Pan SL,Peng CY,Wu PH,Wu WB. Chrysin restores PDGF-induced inhibition on protein tyrosine phosphatase and reduces PDGF signaling in cultured VSMCs. . J Nutr Biochem .2012 ;(23):667-78

80. 2012 Lai MJ,Huang HL,Pan SL,Liu YM,Peng CY,Lee HY, Yeh TK, Huang PH, Teng CM, Chen CS, Chuang HY, Liou JP. Synthesis and biological evaluation of 1-arylsulfonyl-5-(N-hydroxyacrylamide)indoles as potent histone deacetylase inhibitors with antitumor activity in vivo. . J Med Chem .2012 ;(55):3777-91

81. 2012 Chen CH,Liao CH,Chang YL,Guh JH,Pan SL,Teng CM. Protopine, a novel microtubule-stabilizing agent, causes mitotic arrest and apoptotic cell death in human hormone-refractory prostate cancer cell lines. . Cancer Lett .2012 ;(315):1-11

82. 2012 Wang CY,Tsai AC,Peng CY,Chang YL,Lee KH,Teng CM, Pan SL. Dehydrocostuslactone suppresses angiogenesis in vitro and in vivo through inhibition of Akt/GSK-3β and mTOR signaling pathways. . PLoS One .2012 ;(7):e31195-e31195

83. 2012 Chen MC,Pan SL,Shi Q,Xiao Z,Lee KH,Li TK, Teng CM. QS-ZYX-1-61 induces apoptosis through topoisomerase II in human non-small-cell lung cancer A549 cells. . Cancer Sci .2012 ;(103):80-7

84. 2011 Bai LY,Chiu CF,Pan SL,Sargeant AM,Shieh TM,Wang YC, Weng JR. Antitumor activity of a novel histone deacetylase inhibitor (S)-HDAC42 in oral squamous cell carcinoma. . Oral Oncol .2011 ;(47):1127-33

85. 2011 Tsai AC,Pan SL,Lai CY,Wang CY,Chen CC,Shen CC, Teng CM. The inhibition of angiogenesis and tumor growth by denbinobin is associated with the blocking of insulin-like growth factor-1 receptor signaling. . J Nutr Biochem .2011 ;(22):625-33

86. 2011 Yang X,Shi Q,Yang SC,Chen CY,Yu SL,Bastow KF, Morris-Natschke SL, Wu PC, Lai CY, Wu TS, Pan SL, Teng CM, Lin JC, Yang PC, Lee KH. Antitumor agents 288: design, synthesis, SAR, and biological studies of novel heteroatom-incorporated antofine and cryptopleurine analogues as potent and selective antitumor agents. . J Med Chem .2011 ;(54):5097-107

87. 2011 Hsu JL,Pan SL,Ho YF,Hwang TL,Kung FL,Guh JH. Costunolide induces apoptosis through nuclear calcium2+ overload and DNA damage response in human prostate cancer. . J Urol .2011 ;(185):1967-74

88. 2011 Chang LH,Chen CH,Huang DY,Pai HC,Pan SL,Teng CM. Thrombin induces expression of twist and cell motility via the hypoxia-inducible factor-1α translational pathway in colorectal cancer cells. . J Cell Physiol .2011 ;(226):1060-8

89. 2010 Peng CY,Pan SL,Pai HC,Tsai AC,Guh JH,Chang YL, Kuo SC, Lee FY, Teng CM. The indazole derivative YD-3 specifically inhibits thrombin-induced angiogenesis in vitro and in vivo. . Shock .2010 ;(34):580-5

90. 2010 Liu YN,Pan SL,Peng CY,Huang DY,Guh JH,Chen CC, Shen CC, Teng CM. Moscatilin repressed lipopolysaccharide-induced HIF-1alpha accumulation and NF-kappaB activation in murine RAW264.7 cells. . Shock .2010 ;(33):70-5

91. 2010 Tsai AC,Pan SL,Liao CH,Guh JH,Wang SW,Sun HL, Liu YN, Chen CC, Shen CC, Chang YL, Teng CM. Moscatilin, a bibenzyl derivative from the India orchid Dendrobrium loddigesii, suppresses tumor angiogenesis and growth in vitro and in vivo. . Cancer Lett .2010 ;(292):163-70

92. 2010 Dong Y,Shi Q,Pai HC,Peng CY,Pan SL,Teng CM, Nakagawa-Goto K, Yu D, Liu YN, Wu PC, Bastow KF, Morris-Natschke SL, Brossi A, Lee KH. Antitumor agents. 272. Structure-activity relationships and in vivo selective anti-breast cancer activity of novel neo-tanshinlactone analogues. . J Med Chem .2010 ;(53):2299-308

93. 2010 Tsai AC,Pan SL,Sun HL,Wang CY,Peng CY,Wang SW, Chang YL, Kuo SC, Kee KH, Teng CM. CHM-1, a new vascular targeting agent, induces apoptosis of human umbilical vein endothelial cells via p53-mediated death receptor 5 up-regulation. . J Biol Chem .2010 ;(285):5497-506

94. 2010 Chiang PC,Lin SC,Pan SL,Kuo CH,Tsai IL,Kuo MT, Wen WC, Chen P, Guh JH. Antroquinonol displays anticancer potential against human hepatocellular carcinoma cells: a crucial role of AMPK and mTOR pathways. . Biochem Pharmacol .2010 ;(79):162-71

95. 2009 Liu YN,Pan SL,Liao CH,Huang DY,Guh JH,Peng CY, Chang YL, Teng CM. Evodiamine represses hypoxia-induced inflammatory proteins expression and hypoxia-inducible factor 1alpha accumulation in RAW264.7. . Shock .2009 ;(32):263-9

96. 2009 Sun HL,Tsai AC,Pan SL,Ding Q,Yamaguchi H,Lin CN, Hung MC, Teng CM. EPOX inhibits angiogenesis by degradation of Mcl-1 through ERK inactivation. . Clin Cancer Res .2009 ;(15):4904-14

97. 2009 Kuo CT,Chen BC,Yu CC,Weng CM,Hsu MJ,Chen CC, Chen MC, Teng CM, Pan SL, Bien MY, Shih CH, Lin CH. Apoptosis signal-regulating kinase 1 mediates denbinobin-induced apoptosis in human lung adenocarcinoma cells. . J Biomed Sci .2009 ;(16):43

98. 2008 Peng CY,Pan SL,Huang YW,Guh JH,Chang YL,Teng CM. Baicalein attenuates intimal hyperplasia after rat carotid balloon injury through arresting cell-cycle progression and inhibiting ERK, Akt, and NF-kappaB activity in vascular smooth-muscle cells. . Naunyn Schmiedebergs Arch Pharmacol .2008 ;(378):579-88

99. 2008 Chen TH,Pan SL,Guh JH,Chen CC,Huang YT,Pai HC, Teng CM. Denbinobin induces apoptosis by apoptosis-inducing factor releasing and DNA damage in human colorectal cancer HCT-116 cells. . Naunyn Schmiedebergs Arch Pharmacol .2008 ;(378):447-57

100. 2008 Pan SL,Tao KY,Guh JH,Sun HL,Huang DY,Chang YL, Teng CM. The p38 mitogen-activated protein kinase pathway plays a critical role in PAR2-induced endothelial IL-8 production and leukocyte adhesion. . Shock .2008 ;(30):496-502

101. 2008 Wu SY,Pan SL,Chen TH,Liao CH,Huang DY,Guh JH, Chang YL, Kuo SC, Lee FY, Teng CM. YC-1 induces apoptosis of human renal carcinoma A498 cells in vitro and in vivo through activation of the JNK pathway. . Br J Pharmacol .2008 ;(155):505-13

102. 2008 Liu YN,Pan SL,Peng CY,Huang DY,Guh JH,Kuo SC, Lee FY, Teng CM. YC-1 induces heat shock protein 70 expression and prevents oxidized LDL-mediated apoptosis in vascular smooth muscle cells. . Shock .2008 ;(30):274-9

103. 2008 Chen TH,Pan SL,Guh JH,Liao CH,Huang DY,Chen CC, Teng CM. Moscatilin induces apoptosis in human colorectal cancer cells: a crucial role of c-Jun NH2-terminal protein kinase activation caused by tubulin depolymerization and DNA damage. . Clin Cancer Res .2008 ;(14):4250-8

104. 2008 Peng CY,Pan SL,Lee KH,Bastow KF,Teng CM. Molecular mechanism of the inhibitory effect of KS-5 on bFGF-induced angiogenesis in vitro and in vivo. . Cancer Lett .2008 ;(263):114-21

105. 2008 Chiang PC,Hsu JL,Yeh TC,Pan SL,Guh JH. Elucidation of susceptible factors to endoplasmic reticulum stress-mediated anticancer activity in human hepatocellular carcinoma. . Naunyn Schmiedebergs Arch Pharmacol .2008 ;(377):167-77

106. 2008 Kuo CT,Hsu MJ,Chen BC,Chen CC,Teng CM,Pan SL, Lin CH. Denbinobin induces apoptosis in human lung adenocarcinoma cells via Akt inactivation, Bad activation, and mitochondrial dysfunction. . Toxicol Lett .2008 ;(177):48-58

107. 2008 Wang SW,Pan SL,Huang YC,Guh JH,Chiang PC,Huang DY, Kuo SC, Lee KH, Teng CM. CHM-1, a novel synthetic quinolone with potent and selective antimitotic antitumor activity against human hepatocellular carcinoma in vitro and in vivo. . Mol Cancer Ther .2008 ;(7):350-60

研究計畫

計畫名稱
113 研發新穎性標的 RNA splicing 抑制劑用於治療消化道癌症之智慧型藥物設計與轉譯研究-探討 DYRK1/CLK 抑制劑於人類消化道癌進行 mRNA splicing 調控機制和治療潛力(2/3)
補助單位
國家科學及技術委員會

計畫名稱
113 探討 HDAC6 抑制劑治療人類肺腺癌中之潛在生物標記與作用機轉(1/3)
補助單位
國家科學及技術委員會

計畫名稱
113 「探討 HDAC6 抑制劑治療人類肺腺癌中之潛在生物標記與作用機轉」-杜皇儒君
補助單位
國家科學及技術委員會

計畫名稱
112 探討高選擇性 HDAC6 抑制劑在膠質母細 胞瘤之作用機轉
補助單位
國家科學及技術委員會

計畫名稱
112 新穎性DDR1抑制劑對神經膠質母細胞瘤 之效用評估與機轉分析
補助單位
國家科學及技術委員會

計畫名稱
112 新穎藥物細胞測試研究計畫
補助單位
圖策科技股份有限公司

計畫名稱
112 開發天然物及其衍生物應用於阿茲海默症之治療(3/3)
補助單位
國家科學及技術委員會

計畫名稱
112 「開發天然物及其衍生物應用於阿茲海默症之治療」-杜皇儒君
補助單位
國家科學及技術委員會

計畫名稱
112 研發新穎性標的 RNA splicing 抑制劑用於治療消化道癌症之智慧型藥物設計與轉譯研究-探討 DYRK1/CLK 抑制劑於人類消化道癌進行 mRNA splicing 調控機制和治療潛力(1/3)
補助單位
國家科學及技術委員會

計畫名稱
111 研究新穎性藥物DYRK1A抑制劑對於阿茲海默症之治療
補助單位
國家科學及技術委員會

計畫名稱
111 小分子藥物於神經膠質母細胞瘤之細胞作用探討研究計畫
補助單位
智擎生技製藥股份有限公司

計畫名稱
111 開發天然物及其衍生物應用於阿茲海默症之治療(2/3)
補助單位
國家科學及技術委員會

計畫名稱
111 杜皇儒君參與「開發天然物及其衍生物應用於阿茲海默症之治療」研究計畫案,業經核定以「博士級研究人員」資格補助(MOST 110-2811-B-038-507-MY3)(2/3)
補助單位
國家科學及技術委員會

計畫名稱
111 112年度【臨床前藥物研發人工智慧平台】
補助單位
國家科學及技術委員會

計畫名稱
110 研發新穎性MAPK8抑制劑並探討其抗癌功效及作用機轉
補助單位
國家科學及技術委員會

計畫名稱
110 研發急性骨髓性白血病的新穎性CDK8抑制劑並以毒理測試評估其安全性
補助單位
國家科學及技術委員會

計畫名稱
110 開發天然物及其衍生物應用於阿茲海默症之治療(1/3)
補助單位
科技部

計畫名稱
110 補助延攬科技人才杜皇儒君參與「開發天然物及其衍生物應用於阿茲海默症之治療」研究計畫案,業經核定以「博士級研究人員」資格補助(MOST 110-2811-B-038-507-MY3)(1/3)
補助單位
科技部

計畫名稱
109 新穎性選擇性 HDAC6 抑制劑於抗藥性神經膠質母細胞瘤之作用機制探討
補助單位
科技部

計畫名稱
109 研發新穎性 MAP3K9 抑制劑並探討其對胰臟癌之抗癌機轉
補助單位
科技部

計畫名稱
109 研發抗癌小分子 KRAS(G12C) 抑制劑
補助單位
安邦生技股份有限公司

計畫名稱
109 抗癌小分子新藥之臨床前開發與精準治療策略
補助單位
中央研究院

計畫名稱
109 新穎性選擇性HDAC抑制劑之抗癌藥物開發與藥理機轉探討(3/3)
補助單位
科技部

計畫名稱
109 癌症生物學與藥物研發研究所潘秀玲教授申請補助延攬科技人才杜皇儒君參與「新穎性選擇性HDAC抑制劑之抗癌藥物開發與藥理機轉探討」研究計畫案
補助單位
科技部

計畫名稱
109 治療胰臟癌之新穎性標靶藥物開發
補助單位
科技部

計畫名稱
109 治療胰臟癌之新穎性標靶藥物開發
補助單位
醫研生物科技有限公司

計畫名稱
108 The Role of Protein Kinase CK1 and The Mechanism of Inhibitors on Glioblastoma Cells
補助單位
科技部

計畫名稱
108 研發抗癌小分子 KRAS(G12C) 抑制劑
補助單位
安邦生技股份有限公司

計畫名稱
108 新穎性選擇性HDAC抑制劑之抗癌藥物開發與藥理機轉探討(2/3)
補助單位
科技部

計畫名稱
108 「新穎性選擇性HDAC抑制劑之抗癌藥物開發與藥理機轉探討」
補助單位

計畫名稱
107 新穎性選擇性HDAC抑制劑之抗癌藥物開發與藥理機轉探討(1/3)
補助單位
科技部

計畫名稱
107 「新穎性選擇性HDAC抑制劑之抗癌藥物開發與藥理機轉探討」
補助單位

計畫名稱
107 選擇性抗癌標靶藥物HDAC6抑制劑臨床前試驗研究(II)
補助單位
科技部

計畫名稱
106 MPT0145, MPT0L166, MPT0L167, MPT0L184 之抗癌療效評估研究計畫
補助單位
華蔚生物科技股份有限公司

計畫名稱
106 TRB新型抗體藥物動物試驗研究計畫
補助單位
三鈺生物技術股份有限公司

計畫名稱
106 選擇性HDAC1及2抑制劑作為新穎性抗癌藥物之藥物開發與藥理機轉探討
補助單位
科技部

計畫名稱
106 選擇性抗癌標靶藥物HDAC6抑制劑臨床前試驗研究
補助單位
科技部

計畫名稱
106 組蛋白去乙醯?6抑制劑在大腸直腸癌之抗癌機轉探討
補助單位
科技部

計畫名稱
105 新穎性pan-HDAC 抑制劑抑制血管新生之藥物研發與藥理作用機轉(3/3)
補助單位
科技部

計畫名稱
105 新穎性pan-HDAC 抑制劑抑制血管新生之藥物研發與藥理作用機轉(3/3)
補助單位
科技部

計畫名稱
104 MPT0E028 合併療法於胰臟癌與腦癌之研究計畫
補助單位
台新藥股份有限公司

計畫名稱
104 選擇性抗癌標靶藥物HDAC6抑制劑臨床前研究
補助單位
衛生福利部

計畫名稱
104 新穎性pan-HDAC 抑制劑抑制血管新生之藥物研發與藥理作用機轉(2/3)
補助單位
科技部

計畫名稱
104 新穎性pan-HDAC 抑制劑抑制血管新生之藥物研發與藥理作用機轉(2/3)
補助單位
科技部

計畫名稱
104 抗癌藥物 ITCH E3 ubiquitin ligase 抑制劑之臨床前新藥開發- ITCH E3 ubiquitin ligase 抑制劑作為抗癌藥物之臨床前新藥開發(3/3)
補助單位
科技部

計畫名稱
104 抗癌藥物 ITCH E3 ubiquitin ligase 抑制劑之臨床前新藥開發- ITCH E3 ubiquitin ligase 抑制劑作為抗癌藥物之臨床前新藥開發(3/3)
補助單位
台灣泰福生技股份有限公司

計畫名稱
104 選擇性抗癌標靶藥物HDAC6抑制劑臨床前研究(3/3)(相對補助)
補助單位
臺北醫學大學

計畫名稱
103 選擇性抗癌標靶藥物HDAC6抑制劑臨床前研究
補助單位
衛生福利部

計畫名稱
103 抗癌藥物 ITCH E3 ubiquitin ligase 抑制劑之臨床前新藥開發- ITCH E3 ubiquitin ligase 抑制劑作為抗癌藥物之臨床前新藥開發(2/3
補助單位
台灣泰福生技股份有限公司

計畫名稱
103 新穎性PAN-HDAC抑制劑抑制血管新生之藥物研發與藥理作用機轉(1/3)
補助單位
科技部

計畫名稱
103 新穎性pan-HDAC 抑制劑抑制血管新生之藥物研發與藥理作用機轉(1/3)
補助單位
科技部

計畫名稱
103 抗癌藥物ITCH E3 ubiquitin ligase抑制劑之臨床前新藥開發─ITCH E3 ubiquitin ligase抑制劑作為抗癌藥物之臨床前新藥開發(1/3)
補助單位
科技部

計畫名稱
103 產學合作計畫-抗癌藥物ITCH E3 ubiquitin ligase抑制劑之臨床前新藥開發-ITCH E3 ubiquitin ligase抑制劑作為抗癌藥物之臨床前新藥開發(2/3)
補助單位
科技部

計畫名稱
103 產學合作計畫-抗癌藥物ITCH E3 ubiquitin ligase抑制劑之臨床前新藥開發-ITCH E3 ubiquitin ligase抑制劑作為抗癌藥物之臨床前新藥開發(2/3)
補助單位
泰福生技股份有限公司

計畫名稱
102 新穎性抗微管藥物之藥理機轉探討與藥物研發
補助單位
衛生福利部雙和醫院(委託臺北醫學大學興建經營)

計畫名稱
102 選擇性抗癌標靶藥物HDAC6抑制劑臨床前研究
補助單位
衛生福利部

計畫名稱
102 產學合作計畫-抗癌藥物ITCH E3 UBIQUITIN LIGASE抑制劑之臨床前新藥開發-ITCH E3 UBIQUITIN LIGASE抑制劑作為抗癌藥物之臨床前新藥開發(1-3)
補助單位
科技部

計畫名稱
102 產學合作計畫-抗癌藥物ITCH E3 UBIQUITIN LIGASE抑制劑之臨床前新藥開發-ITCH E3 UBIQUITIN LIGASE抑制劑作為抗癌藥物之臨床前新藥開發(1-3)-泰福
補助單位
泰福生技股份有限公司

計畫名稱
102 核甘類候選藥物之小鼠口服毒理測試及療效評估
補助單位
博研醫藥開發股份有限公司

計畫名稱
101 以 Histone deacetylases 抑制劑作為抗癌藥物之研發(3/3)
補助單位
行政院國家科學委員會

計畫名稱
101 TMU101-AE1-B48
補助單位
學校