标题:MDR1 (multidrug resistence 1) can regulate GCS (glucosylceramide synthase) in breast cancer cells.
作者:Zhang X;Wu X;Li J;Sun Y;Gao P;Zhang C;Zhang H;Zhou G
作者机构:[Zhang, X] Department of Pathology, Shandong University, School of Medicine, 44#, Wenhua Xi Road, Jinan, Shandong, 250012, China;[ Wu, X] Department o 更多
通讯作者:Zhou, GY
通讯作者地址:[Zhou, GY]Shandong Univ, Dept Pathol, Sch Med, 44 Wenhua Xi Rd, Jinan 250012, Shandong, Peoples R China.
来源:Journal of Surgical Oncology
出版年:2011
卷:104
期:5
页码:466-471
DOI:10.1002/jso.21958
关键词:multidrug resistance gene-1; glucosylceramide synthase; multidrug; resistance; breast cancer
摘要:BACKGROUND AND OBJECTIVES: Besides MDR1/P-glycoprotein (MDR1/P-gp), glucosylceramide synthase (GCS), an enzyme, which transfers UDP-glucose to ceramide to form glucosylceramide was also related with multidrug resistance (MDR) in breast cancer. Although many research showed that GCS could affect mdr1 in cancer cells, nobody knows that whether mdr1 can affect GCS in breast cancer. Our study aims to verify that. METHODS: A plasmid with multidrug resistence 1(mdr1) cDNA was transfected into the sensitive breast cancer cell line MCF-7, while an RNA interference (RNAi) vector targeted mdr1 was transfected into the MDR cell line MCF-7/ADM. Then RT-PCR, Western blot, MTT, and flow cytometry were used to assess the expression and function of mdr1 and GCS. RESULT: The data displayed that up-regulation of mdr1 could increase the expression of GCS, while the RNAi-expression plasmids could decrease that. Meantime, the changes of ceramide are opposed to that of GCS and are the same to the alteration of apoptosis rate. CONCLUSIONS: Our results demonstrate that MDR1 could increase cellular apoptosis by regulating the expression of GCS in breast cancer cells.
收录类别:SCOPUS;SCIE
WOS核心被引频次:10
Scopus被引频次:11
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-79961060309&doi=10.1002%2fjso.21958&partnerID=40&md5=bf39c4c8bdfde7a794764eb8f42d320a
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