Shu-Ming Tsao

Dr. Shu-Ming Tsao

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Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

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

Representative Publications

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27 January 2020 in The Plant Cell
Verified
Journal Article
Open access
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WLWen-Chi Lee
Wen-Chi Lee
BHBo-Han Hou
Bo-Han Hou
CHCheng-Yu Hou
Cheng-Yu Hou
STShu-Ming Tsao
Shu-Ming Tsao
PKPing Kao
Ping Kao
HCHo-Ming Chen
Ho-Ming Chen
Exon junction complex footprints account for a sizable proportion of major RNA degradation intermediates and can serve as markers for mRNA degradation before st

13 December 2021 in Polymers
Verified
Journal Article
Open access
PDF file
WQWei-Lun Qiu
Wei-Lun Qiu
WHwei-hung Hsu
wei-hung Hsu
STShu-Ming Tsao
Shu-Ming Tsao
ATAi-Jung Tseng
Ai-Jung Tseng
ZLZhi-hu Lin
Zhi-hu Lin
TLTung-Yi Lin
Tung-Yi Lin
Lung cancer has the highest global mortality rate of any cancer. Although targeted therapeutic drugs are commercially available, the common drug resistance and insensitivity to cisplatin-based chemotherapy, a common clinical treatment for lung cancer, have prompted active research on alternative lung cancer therapies and methods for mitigating cisplatin-related complications. In this study, we investigated the effect of WSG, a glucose-rich, water soluble polysaccharide derived from Ganoderma lucidum, on cisplatin-based treatment for lung cancer. Murine Lewis lung carcinoma (LLC1) cells were injected into C57BL/6 mice subcutaneously and through the tail vein. The combined administration of WSG and cisplatin effectively inhibited tumor growth and the formation of metastatic nodules in the lung tissue of the mice. Moreover, WSG increased the survival rate of mice receiving cisplatin. Co-treatment with WSG and cisplatin induced a synergistic inhibitory effect on the growth of lung cancer cells, enhancing the apoptotic responses mediated by cisplatin. WSG also reduced the cytotoxic effect of cisplatin in both macrophages and normal lung fibroblasts. Our findings suggest that WSG can increase the therapeutic effectiveness of cisplatin. In clinical settings, WSG may be used as an adjuvant or supplementary agent.

1 October 2021 in Phytopathology®
Verified
Journal Article
Closed access
YTYuh Tzean
Yuh Tzean
BHBo-Han Hou
Bo-Han Hou
STShu-Ming Tsao
Shu-Ming Tsao
HCHo-Ming Chen
Ho-Ming Chen
ACAn-Po Cheng
An-Po Cheng
Hsin-Hung YehHsin-Hung Yeh
Hsin-Hung Yeh
Bananas are among the world’s most important cash and staple crops but are threatened by various devastating pathogens. The phytohormone salicylic acid (SA) plays a key role in the regulation of plant immune response. Tracking the expression of SA-responsive marker genes under pathogen infection is important in pathogenesis elucidation. However, the common SA-responsive marker genes are not consistently induced in different banana cultivars or different organs. Here, we conducted transcriptome analysis for SA response of a banana cultivar, ‘Pei-Chiao’ (Cavendish, AAA genome), and identified three genes, MaWRKY40, MaWRKY70, and Downy Mildew Resistant 6 (DMR6)-Like Oxygenase 1 (MaDLO1) that are robustly induced upon SA treatment in both the leaves and roots. Consistent induction of these three genes by SA treatment was also detected in both the leaves and roots of bananas belonging to different genome types such as ‘Tai-Chiao No. 7’ (Cavendish, AAA genome), ‘Pisang Awak’ (ABB genome), and ‘Lady Finger’ (AA genome). Furthermore, the biotrophic pathogen cucumber mosaic virus elicited the expression of MaWRKY40 and MaDLO1 in infected leaves of susceptible cultivars. The hemibiotrophic fungal pathogen Fusarium oxysporum f. sp. cubense tropical race 4 (TR4) also consistently induced the expression of MaWRKY40 and MaDLO1 in the infected roots of the F. oxysporum f. sp. cubense TR4-resistant cultivar. These results indicate that MaWRKY40 and MaDLO1 can be used as reliable SA-responsive marker genes for the study of plant immunity in banana. Revealing SA-responsive marker genes provides a stepping stone for further studies in banana resistance to pathogens.