a new mixed-backbone oligonucleotide against glucosylceramide synthase sensitizes multidrug-resistant tumors to apoptosis一个新的mixed-backbone寡核苷酸对葡糖神经酰胺合成酶糖分会让耐多药肿瘤细胞凋亡.pdfVIP
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a new mixed-backbone oligonucleotide against glucosylceramide synthase sensitizes multidrug-resistant tumors to apoptosis一个新的mixed-backbone寡核苷酸对葡糖神经酰胺合成酶糖分会让耐多药肿瘤细胞凋亡
A New Mixed-Backbone Oligonucleotide against
Glucosylceramide Synthase Sensitizes
Multidrug-Resistant Tumors to Apoptosis
1 2 1,7 1 3 4
Gauri A. Patwardhan , Qian-Jin Zhang , Dongmei Yin , Vineet Gupta , Jianxiong Bao , Can E. Senkal ,
4 5 1 1 6
Besim Ogretmen , Myles C. Cabot , Girish V. Shah , Paul W. Sylvester , S. Michal Jazwinski ,
Yong-Yu Liu1*
1 Department of Basic Pharmaceutical Sciences, University of Louisiana at Monroe, Monroe, Louisiana, United States of America, 2 Department of Cellular Biology and
Anatomy, Louisiana State University Health Sciences Center, Shreveport, Louisiana, United States of America, 3 Department of Pathology, Louisiana State University Health
Sciences Center, Shreveport, Louisiana, United States of America, 4 Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston,
South Carolina, United States of America, 5 Experimental Therapeutics, John Wayne Cancer Institute, Santa Monica, California, United States of America, 6 Department of
Medicine, Tulane University School of Medicine, New Orleans, Louisiana, United States of America, 7 Department of Biochemistry, Nantong University School of Medicine,
Nantong, Jiangsu, China
Abstract
Enhanced ceramide glycosylation catalyzed by glucosylceramide synthase (GCS) limits therapeutic efficiencies of
antineoplastic agents including doxorubicin in drug-resistant cancer cells. Aimed to determine the role of GCS in tumor
response to chemotherapy, a new mixed-backbone oligonucleotide (MBO-asGCS) with higher stability and efficiency has
been generat
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