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Full-time Faculty

Jih-Hwa Guh

Field of study:Mechanism research of anticancer drugs
Telephone:(02)3366-8761
E-mail:jhguh@ntu.edu.tw
My job:Professor
Personal website:https://scholars.lib.ntu.edu.tw/cris/rp/rp06467

Education : 1992/09~1996/06 Ph.D. Pharmacology N.T.U.
1990/09~1992/06 M.S. Pharmacology N.T.U.
1986/09~1990/06 B.S. Pharmacy N.T.U.
Experience : From 2010/Aug Professor, School of Pharmacy, NTU
2008/Jul~2009/Jul Visiting Associate Professor, The Ohio State University
2004/8~2010/Jul Associate Professor, School of Pharmacy, NTU
2000/2- 2004/7 Assistant Professor, School of Pharmacy, NTU
1996/10-2000/1 Post-Doctor, Drug Development and Research Center, NTU
Research Areas : Mechanism research of anticancer drugs
Lab Focus : We focus the research interests on the development of anticancer agents. We have developed an assay system to do a large scale of screening tests to discover potential agents against cancers. In recent years, we have screened more than 4000 samples from both chemically synthetic compounds and natural products. The mechanisms of the anticancer abilities of effective compounds were studied in this program. Accordingly, a lot of cellular signals being targeted by these compounds have been identified, such as Cdk/cyclin complexes, Cdk inhibitors (p21 and p27), tubulin, topoisomerases, AMPK, ER stress and DNA damage response. Take antroquinonol as an example. Antroquinonol that was isolated from Antrodia camphorate, a well-known Traditional Chinese Medicine for treatment of liver diseases, displayed effective anticancer activity against numerous hepatocellular carcinoma cell lines. Antroquinonol is capable of stimulating AMPK activation, inducing the assembly of tuberous sclerosis complex (TSC)-1/TSC2 and leading to the blockade of cellular protein synthesis through inhibition of protein phosphorylation including mTOR (Ser2448), p70S6K (Thr421/Ser424 and Thr389) and 4E-BP1 (Thr37/Thr46 and Thr70). The inhibition of mTOR signaling pathway leads to the cell-cycle arrest at G1 phase which, ultimately, causes apoptotic cell death.
Research Subjects : 1. Pharmacological evaluation of anticancer activity of chemically synthetic compounds and natural products.
2. Mechanism study of anticancer agents.

Establishing a noncanonical zinc-binding group as a selective histone deacetylase inhibitor and possible novel anticancer agent.
(2025-10) Huang, Hsuan-Chun ; Chen, Tse-Yu ; Yeh, Tsung-Yu ; Yu, Min-Hsuan ; Wu, Sian-Siou ; Li, Guang-Yi ; Chen, Bo-Yu ; MIAO-HSIA LIN ; Lin, Ching-Jung ; Hsu, Jui-Ling ; JIH-HWA GUH ; CHAO-WU YU

Design and synthesis of novel HDAC6 inhibitor dimer as HDAC6 degrader for cancer treatment by palladium catalysed dimerisation.
(2025) Lin, Ching ; Hsu, Jui-Ling ; Hsu, Yu-Tung ; Fan, Kuo-Chen ; Wu, Sian-Siou ; MIAO-HSIA LIN ; JIH-HWA GUH ; CHAO-WU YU

Doxazosin inhibits vasculogenic mimicry in human non‑small cell lung cancer through inhibition of the VEGF‑A/VE‑cadherin/mTOR/MMP pathway
(2024-04) Hsu, Jui-Ling ; Leu, Wohn-Jenn ; LIH-CHING HSU ; Hsieh, Chia-Hsun ; JIH-HWA GUH

Cardenolide glycosides sensitize gefitinib-induced apoptosis in non-small cell lung cancer: inhibition of Na+/K+-ATPase serving as a switch-on mechanism
(2024-03-07) Du, Chi-Min ; Leu, Wohn-Jenn ; Jiang, Yi-Huei ; Chan, She-Hung ; Chen, Ih-Sheng ; Chang, Hsun-Shuo ; LIH-CHING HSU ; Hsu, Jui-Ling ; JIH-HWA GUH

A novel HDAC6 inhibitor interferes microtubule dynamics and spindle assembly checkpoint and sensitizes cisplatin-induced apoptosis in castration-resistant prostate cancer
(2024-02-20) Ye, Pei-Chen ; Leu, Wohn-Jenn ; Yeh, Tsung-Yu ; Hsu, Yu-Tung ; Lin, Yi-Chin ; Wei, Zi-Yuan ; Chen, Yi-Chin ; Chiang, Yi-Chang ; Hsu, Jui-Ling ; Chan, She-Hung ; LIH-CHING HSU ; JI-WANG CHERN ; CHAO-WU YU ; JIH-HWA GUH

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Study of Active Extract from Traditional Chinese Medicine Formula on Anti-Non-Small Cell Lung Cancer Effect
(2023-08-01~) JIH-HWA GUH

Study of Active Extract from Traditional Chinese Medicine Formula on Anti-Non-Small Cell Lung Cancer Effect
(2022-08-01~) JIH-HWA GUH

Study of Active Extract from Traditional Chinese Medicine Formula on Anti-Non-Small Cell Lung Cancer Effect
(2021-08-01~) JIH-HWA GUH

Design, Synthesis and Mechanism Study of Anticancer Agents on Akt Inhibition and Lipid Raft Disturbing against Human Hormone-Refractory Metastatic Prostate Cancer
(2020-08-01~) JIH-HWA GUH

Design, Synthesis and Mechanism Study of Anticancer Agents on Akt Inhibition and Lipid Raft Disturbing against Human Hormone-Refractory Metastatic Prostate Cancer
(2019-08-01~) JIH-HWA GUH

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