G
Gi Ming Lai
Researcher at Taipei Medical University
Publications - 36
Citations - 1478
Gi Ming Lai is an academic researcher from Taipei Medical University. The author has contributed to research in topics: Apoptosis & Cancer cell. The author has an hindex of 18, co-authored 34 publications receiving 1325 citations. Previous affiliations of Gi Ming Lai include National Health Research Institutes & Memorial Hospital of South Bend.
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Journal ArticleDOI
Receptor tyrosine kinase AXL is induced by chemotherapy drugs and overexpression of AXL confers drug resistance in acute myeloid leukemia
Chih Chen Hong,Jong Ding Lay,Jhy Shrian Huang,Ann-Lii Cheng,Ann-Lii Cheng,Jih-Luh Tang,Ming Tseh Lin,Gi Ming Lai,Shuang En Chuang +8 more
TL;DR: Results show that upregulation of AXL by chemotherapy might induce drug resistance in acute myeloid leukemia in the presence of Gas6 stimulation.
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Basal levels and patterns of anticancer drug-induced activation of nuclear factor-κB (NF-κB), and its attenuation by tamoxifen, dexamethasone, and curcumin in carcinoma cells☆
TL;DR: It is demonstrated that activation of NF-kappaB is a general cellular response to anticancer drugs, and the mechanism of activation appears to be distinct from that induced by TNF-alpha.
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Cytotoxic triterpenes from Antrodia camphorata and their mode of action in HT-29 human colon cancer cells
Chi-tai Yeh,Yerra Koteswara Rao,Chih Jung Yao,Chuan Feng Yeh,Chi Han Li,Shuang En Chuang,John H. T. Luong,Gi Ming Lai,Gi Ming Lai,Yew Min Tzeng +9 more
TL;DR: Five lanostane (2, 3, 4, 6 and 8) and three ergostane-type triterpenes isolated from the fruiting bodies of Antrodia camphorata were evaluated for their in vitro cytotoxic data against various cancer cell types.
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Sulfasalazine Suppresses Drug Resistance and Invasiveness of Lung Adenocarcinoma Cells Expressing AXL
Jong Ding Lay,Chih Chen Hong,Jhy Shrian Huang,Ya Yu Yang,Chung Yi Pao,Ching Hang Liu,Yi Pin Lai,Gi Ming Lai,Ann-Lii Cheng,Ih-Jen Su,Shuang En Chuang +10 more
TL;DR: Sulfasalazine exerted a synergistic anticancer effect with doxorubicin and suppressed cancer cell invasiveness in parallel in CL1 sublines and various AXL-expressing cancer cell lines, suggesting that AXL is involved in NSCLC metastasis and drug resistance and may therefore provide a molecular basis for RTK-targeted therapy using sulfasalazines to enhance the efficacy of chemotherapy inNSCLC.
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Identification and characterization of a novel gene Saf transcribed from the opposite strand of Fas
TL;DR: It is suggested that Saf might protect T lymphocytes from Fas-mediated apoptosis by blocking the binding of FasL or its agonistic Fas antibody, and might regulate the expression of Fas alternative splice forms through pre-mRNA processing.