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黄芩素通过下调 IKZF1 和 IKZF3 抑制骨髓瘤 U266 细胞的增殖。

Baicalein Inhibits Proliferation of Myeloma U266 Cells by Downregulating IKZF1 and IKZF3.

机构信息

Center for Evidence-Based and Translational Medicine, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China (mainland).

Department of Hematology, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China (mainland).

出版信息

Med Sci Monit. 2018 May 5;24:2809-2817. doi: 10.12659/MSM.907058.

Abstract

BACKGROUND Baicalein can suppress the growth of multiple tumors, including multiple myeloma (MM), but the exact mechanisms remains elusive. Here, we investigated the exact mechanisms of the anti-myeloma activity of baicalein. MATERIAL AND METHODS Proliferation and rates of apoptosis of myeloma U266 cells exposed to baicalein were detected. Microarray, polymerase chain reaction (PCR) assay, and Western blot analysis were applied to evaluate the mRNA and protein levels of associated molecules. Survival analysis of IKZF1 and IKZF3 was conducted as well. RESULTS Baicalein suppressed the growth and stimulated apoptosis of myeloma U266 cells in a dose- and time-dependent way. Baicalein increased mRNA level of CRBN, and further studies suggested that baicalein downregulated IKZF1 and IKZF3 on a post-transcriptional level. Although the differences did not reach statistical significance, IKZF1 and IKZF3 were associated with poor overall survival. CONCLUSIONS Our results suggest that baicalein suppresses the growth and promotes apoptosis of myeloma U266 cells through downregulating IKZF1 and IKZF3. Baicalein increased the expression of CRBN, which might exert a reversion effect on resistance of IMiDs. MM patients in IKZF1 and IKZF3 low-expression groups had better overall survival than those in IKZF1 and IKZF3 high-expression groups. Thus, the present results indicate that baicalein might be a therapeutic choice for targeting IKZF1 and IKZF3.

摘要

背景

黄芩素可以抑制多种肿瘤的生长,包括多发性骨髓瘤(MM),但其确切机制仍不清楚。在这里,我们研究了黄芩素抗骨髓瘤活性的确切机制。

材料和方法

检测黄芩素处理的骨髓瘤 U266 细胞的增殖和凋亡率。应用微阵列、聚合酶链反应(PCR)检测和 Western blot 分析评估相关分子的 mRNA 和蛋白水平。同时进行 IKZF1 和 IKZF3 的生存分析。

结果

黄芩素呈剂量和时间依赖性抑制骨髓瘤 U266 细胞的生长并刺激其凋亡。黄芩素增加了 CRBN 的 mRNA 水平,进一步的研究表明,黄芩素在转录后水平下调了 IKZF1 和 IKZF3。虽然差异没有达到统计学意义,但 IKZF1 和 IKZF3 与总体生存不良相关。

结论

我们的结果表明,黄芩素通过下调 IKZF1 和 IKZF3 抑制骨髓瘤 U266 细胞的生长并促进其凋亡。黄芩素增加了 CRBN 的表达,这可能对 IMiDs 耐药产生逆转作用。IKZF1 和 IKZF3 低表达组的 MM 患者的总体生存率高于 IKZF1 和 IKZF3 高表达组。因此,本研究结果表明,黄芩素可能是针对 IKZF1 和 IKZF3 的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26de/5958785/c25fc31104ea/medscimonit-24-2809-g001.jpg

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