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pubmed-article:21030352pubmed:abstractTextA number of growth factors secreted by bone marrow stromal cells (BMSCs), including interleukin-6 and -8 (IL-6/8), are important for the initiation and progression of multiple myeloma (MM). However, the mechanisms that regulate the production of IL-6/8 by BMSC have not yet been well characterized. Human dual functional protein apurinic/apyrimidinic endonuclease-1/redox factor-1 (APE1/Ref-1) is essential for cell survival and proliferation. Previous studies showed that APE1/Ref-1 was overexpressed in tumor cells, but few studies showed its expression in supportive cells in the tumor microenvironment. We first detected APE1/Ref-1 expression in BMSCs of normal, initial, and recurrent MM patients, and then explore the correlation between APE1/Ref-1 level and IL-6/8 secretion of BMSCs. A marked increase of APE1/Ref-1 expression and abnormal subcellular distribution were observed in MM BMSCs. APE1/Ref-1 overexpression was related to higher secretary level of IL-6/8 by MM BMSCs and the IL-6/8 secretion was blocked significantly by adenovirus-mediated APE1/Ref-1-specific (small interfering RNA) siRNA. Our results also demonstrated that APE1/Ref-1-specific siRNA significantly inhibited DNA binding activity of AP-1 and nuclear factor-?B (NF-?B), 2 important transcription factors in the regulation IL-6/8 secretion in MM BMSCs. The results provided by the present study indicate APE1/Ref-1, which plays a regulatory role in IL-6/8 production by BMSCs, may be a potential therapeutic target of MM.lld:pubmed
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pubmed-article:21030352pubmed:authorpubmed-author:HuntM FMFlld:pubmed
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pubmed-article:21030352pubmed:authorpubmed-author:ZengLin-LiLLlld:pubmed
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pubmed-article:21030352pubmed:articleTitleElevated expression of APE1/Ref-1 and its regulation on IL-6 and IL-8 in bone marrow stromal cells of multiple myeloma.lld:pubmed
pubmed-article:21030352pubmed:affiliationResearch Institute of Surgery, Cancer Center, Daping Hospital, Third Military Medical University, Chongqing China.lld:pubmed
pubmed-article:21030352pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:21030352pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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