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多发性骨髓瘤骨髓基质细胞中 APE1/Ref-1 的高表达及其对 IL-6 和 IL-8 的调控。

Elevated expression of APE1/Ref-1 and its regulation on IL-6 and IL-8 in bone marrow stromal cells of multiple myeloma.

机构信息

Research Institute of Surgery, Cancer Center, Daping Hospital, Third Military Medical University, Chongqing China.

出版信息

Clin Lymphoma Myeloma Leuk. 2010 Oct;10(5):385-93. doi: 10.3816/CLML.2010.n.072.

Abstract

A 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-κB (NF-κB), 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.

摘要

许多由骨髓基质细胞(BMSCs)分泌的生长因子,包括白细胞介素 6 和 8(IL-6/8),对于多发性骨髓瘤(MM)的起始和进展非常重要。然而,调节 BMSC 产生 IL-6/8 的机制尚未得到很好的描述。人双功能蛋白脱嘌呤/脱嘧啶核酸内切酶-1/氧化还原因子-1(APE1/Ref-1)对于细胞存活和增殖是必需的。先前的研究表明,APE1/Ref-1 在肿瘤细胞中过表达,但很少有研究表明其在肿瘤微环境中的支持细胞中表达。我们首先检测了正常、初发和复发性 MM 患者的 BMSCs 中 APE1/Ref-1 的表达,然后探讨了 APE1/Ref-1 水平与 BMSCs 分泌 IL-6/8 的相关性。在 MM BMSCs 中观察到 APE1/Ref-1 表达的显著增加和异常的亚细胞分布。APE1/Ref-1 过表达与 MM BMSCs 分泌更高水平的 IL-6/8 有关,而腺病毒介导的 APE1/Ref-1 特异性(小干扰 RNA)siRNA 可显著阻断 IL-6/8 的分泌。我们的结果还表明,APE1/Ref-1 特异性 siRNA 可显著抑制 AP-1 和核因子-κB(NF-κB)的 DNA 结合活性,这两种转录因子在调节 MM BMSCs 中 IL-6/8 的分泌中起重要作用。本研究提供的结果表明,APE1/Ref-1 在调节 BMSCs 产生 IL-6/8 中发挥调节作用,可能是 MM 的一个潜在治疗靶点。

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