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脑源性神经营养因子VAL66MET多态性通过微泡中的微小RNA-146b增加膀胱癌风险。

BDNF VAL66MET Polymorphism Elevates the Risk of Bladder Cancer via MiRNA-146b in Micro-Vehicles.

作者信息

Li Cong, Zeng Xing, Liu Zheng, Li Fan, Wang Kun, Wu Baisen

出版信息

Cell Physiol Biochem. 2018;45(1):366-377. doi: 10.1159/000486908. Epub 2018 Jan 22.

Abstract

BACKGROUND/AIMS: Emerging studies on brain-derived neurotrophic factor (BDNF) have shown that might be novel biomarkers and therapeutic targets for cancer. We explore the role of BDNF in the tumorigenesis of bladder cancer and the underlying molecular mechanism.

METHODS

368 patients with diagnosed bladder cancer and 352 healthy controls were enrolled to evaluate the association of BDNF and the miR-146b. Bioinformatics algorithm analysis and luciferase assay were performed to identify the target genes of miR-146b. Real-time PCR and western-blot were carried out to validate the relationship between miR-146b and CRK. MTT assay and FACS were used to evaluated the proliferation and apoptosis of cancer cells. MVs were isolated and transfect into the culture cells to confirm the above observation.

RESULTS

The clinical study shows that BDNF Met/Met was significantly associated with the risk of bladder cancer. In addition, comparing with Val/Val and Val/Met, Met/Met has lower miR-146b level. Luciferase assay shows that BDNF Val/Val is apparently enhanced miR-146b promoter-luciferase, but not BDNF Met/Met. Based on luciferase assay, CRK is a direct target gene of miR-146b. MiR-146b mimics significantly inhibited the expression of CRK and activation of AKT level. The expression of CRK and the activation of AKT (p-AKT) were significantly inhibited by MV-BDNF Val/Val-miR-146b or MV-BDNF Val/Met-miR-146b, but not MV-BDNF Met/Met-miR-146b. MV-BDNF Val/Val-miR-146b or Val/Met-miR-146b obviously inhibited cell proliferation, which eliminated by CRK. Meanwhile, with MV-BDNF Met/Met-miR-146b or Met/Met-miR-146b+CRK did not affect the proliferation. MV-BDNF Val/Val-miR-146b or Val/Met-miR-146b enhanced cell apoptosis, which could be eliminated by CRK. Meanwhile, MV-BDNF Met/Met-miR-146b or Met/Met-miR-146b+CRK did not promote apoptosis.

CONCLUSION

BDNF VAL66MET polymorphism is associated with miR-146b and its target gene CRK. MiR-146b and CRK mediated BDNF VAL66MET polymorphism associated proliferation and apoptosis via activation of AKT. Thus, BDNF Val66Met is associated with the risk of bladder cancer, and the BDNF variant could be used a biomarker for the diagnosis of bladder cancer.

摘要

背景/目的:关于脑源性神经营养因子(BDNF)的新研究表明,其可能是癌症的新型生物标志物和治疗靶点。我们探讨了BDNF在膀胱癌发生发展中的作用及其潜在分子机制。

方法

纳入368例确诊膀胱癌患者和352例健康对照,评估BDNF与miR-146b的相关性。采用生物信息学算法分析和荧光素酶报告基因检测鉴定miR-146b的靶基因。进行实时定量PCR和蛋白质免疫印迹法验证miR-146b与CRK的关系。采用MTT法和流式细胞术评估癌细胞的增殖和凋亡。分离微泡并转染至培养细胞以证实上述观察结果。

结果

临床研究表明,BDNF Met/Met与膀胱癌风险显著相关。此外,与Val/Val和Val/Met相比,Met/Met的miR-146b水平较低。荧光素酶报告基因检测表明,BDNF Val/Val明显增强miR-146b启动子荧光素酶活性,而BDNF Met/Met则无此作用。基于荧光素酶报告基因检测,CRK是miR-146b的直接靶基因。miR-146b模拟物显著抑制CRK表达和AKT水平的激活。MV-BDNF Val/Val-miR-146b或MV-BDNF Val/Met-miR-146b显著抑制CRK表达和AKT(p-AKT)激活,但MV-BDNF Met/Met-miR-146b无此作用。MV-BDNF Val/Val-miR-146b或Val/Met-miR-146b明显抑制细胞增殖,而CRK可消除这种抑制作用。同时,MV-BDNF Met/Met-miR-146b或Met/Met-miR-146b+CRK对细胞增殖无影响。MV-BDNF Val/Val-miR-146b或Val/Met-miR-146b增强细胞凋亡,CRK可消除这种增强作用。同时,MV-BDNF Met/Met-miR-146b或Met/Met-miR-146b+CRK不促进细胞凋亡。

结论

BDNF VAL66MET多态性与miR-146b及其靶基因CRK相关。miR-146b和CRK通过激活AKT介导BDNF VAL66MET多态性相关的增殖和凋亡。因此,BDNF Val66Met与膀胱癌风险相关,该BDNF变体可作为膀胱癌诊断的生物标志物。

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