Cheng-Wen Lin

Prof. Dr. Cheng-Wen Lin

Department of Medical Laboratory Science and Biotechnology, China Medical University, Taichung 404, Taiwan
orcid

Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2005 in Antiviral Research
Verified
Journal Article
Closed access
Cheng-Wen LinCheng-Wen Lin
Cheng-Wen Lin
FTFuu-Jen Tsai
Fuu-Jen Tsai
CTChang-Hai Tsai
Chang-Hai Tsai
CLChien-Chen Lai
Chien-Chen Lai
LWLei Wan
Lei Wan
PCPei-Dawn Lee Chao
Pei-Dawn Lee Chao

11 May 2010 in Journal of Biomedical Science
Verified
Journal Article
Open access
PDF file
HHHsiang-Ling Huang
Hsiang-Ling Huang
HHHsiang-Wei Hsing
Hsiang-Wei Hsing
TLTzu-Chia Lai
Tzu-Chia Lai
YCYi-Wen Chen
Yi-Wen Chen
TLTian-Ren Lee
Tian-Ren Lee
HCHong-Lin Chan
Hong-Lin Chan
Background: It is essential to subculture the cells once cultured cells reach confluence. For this, trypsin is frequently applied to dissociate adhesive cells from the substratum. However, due to the proteolytic activity of trypsin, cell surface proteins are often cleaved, which leads to dysregulation of the cell functions. Methods: In this study, a triplicate 2D-DIGE strategy has been performed to monitor trypsin-induced proteome alterations. The differentially expressed spots were identified by MALDI-TOF MS and validated by immunoblotting. Results: 36 proteins are found to be differentially expressed in cells treated with trypsin, and proteins that are known to regulate cell metabolism, growth regulation, mitochondrial electron transportation and cell adhesion are down-regulated and proteins that regulate cell apoptosis are up-regulated after trypsin treatment. Further study shows that bcl-2 is down-regulated, p53 and p21 are both up-regulated after trypsinization. Conclusions: In summary, this is the first report that uses the proteomic approach to thoroughly study trypsin-induced cell physiological changes and provides researchers in carrying out their experimental design.

1 December 2008 in Cancer Letters
Verified
Journal Article
Closed access
SLSong-Shei Lin
Song-Shei Lin
HHHsuan-Pang Huang
Hsuan-Pang Huang
JYJai-Sing Yang
Jai-Sing Yang
JWJeng-Yuan Wu
Jeng-Yuan Wu
THTe-Chun Hsai
Te-Chun Hsai
JCJing-Gung Chung
Jing-Gung Chung

1 November 2010 in Analytica Chimica Acta
Verified
Journal Article
Closed access
YJYu-Jen Jou
Yu-Jen Jou
CLChia-Der Lin
Chia-Der Lin
CLChih-Ho Lai
Chih-Ho Lai
CCChao-Hsien Chen
Chao-Hsien Chen
JKJung-Yie Kao
Jung-Yie Kao
Cheng-Wen LinCheng-Wen Lin
Cheng-Wen Lin

27 February 2020 in Biomolecules
Verified
Journal Article
Open access
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YTYu-Chi Tsai
Yu-Chi Tsai
CLCHIA-LIN Lee
CHIA-LIN Lee
HYHung-Rong Yen
Hung-Rong Yen
YCYoung-Sheng Chang
Young-Sheng Chang
YLYu-Ping Lin
Yu-Ping Lin
Cheng-Wen LinCheng-Wen Lin
Cheng-Wen Lin
Strobilanthes cusia (Nees) Kuntze is a Chinese herbal medicine used in the treatment of respiratory virus infections. The methanol extract of S. cusia leaf contains chemical components such as β-sitosterol, indirubin, tryptanthrin, betulin, indigodole A, and indigodole B that have diverse biological activities. However, the antiviral action of S. cusia leaf and its components against human coronavirus remains to be elucidated. Human coronavirus NL63 infection is frequent among immunocompromised individuals, young children, and in the elderly. This study investigated the anti-Human coronavirus NL63 (HCoV-NL63) activity of the methanol extract of S. cusia leaf and its major components. The methanol extract of S. cusia leaf effectively inhibited the cytopathic effect (CPE) and virus yield (IC50 = 0.64 μg/mL) in HCoV-NL63-infected cells. Moreover, this extract potently inhibited the HCoV-NL63 infection in a concentration-dependent manner. Among the six components identified in the methanol extract of S. cusia leaf, tryptanthrin and indigodole B (5aR-ethyltryptanthrin) exhibited potent antiviral activity in reducing the CPE and progeny virus production. The IC50 values against virus yield were 1.52 μM and 2.60 μM for tryptanthrin and indigodole B, respectively. Different modes of time-of-addition/removal assay indicated that tryptanthrin prevented the early and late stages of HCoV-NL63 replication, particularly by blocking viral RNA genome synthesis and papain-like protease 2 activity. Notably, tryptanthrin (IC50 = 0.06 μM) and indigodole B (IC50 = 2.09 μM) exhibited strong virucidal activity as well. This study identified tryptanthrin as the key active component of S. cusia leaf methanol extract that acted against HCoV-NL63 in a cell-type independent manner. The results specify that tryptanthrin possesses antiviral potential against HCoV-NL63 infection.

1 November 2019 in Virus Research
Verified
Journal Article
Closed access
JWJing-Ru Weng
Jing-Ru Weng
CLChen-Sheng Lin
Chen-Sheng Lin
HLHsueh-Chou Lai
Hsueh-Chou Lai
YLYu-Ping Lin
Yu-Ping Lin
CWChing-Ying Wang
Ching-Ying Wang
Cheng-Wen LinCheng-Wen Lin
Cheng-Wen Lin