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纳米囊泡是监测前列腺癌碳离子放射治疗疗效的潜在工具。

Nano-Vesicles are a Potential Tool to Monitor Therapeutic Efficacy of Carbon Ion Radiotherapy in Prostate Cancer.

作者信息

Yu Qi, Li Ping, Weng Meilin, Wu Shuang, Zhang Yafang, Chen Xue, Zhang Qing, Shen Guangxia, Ding Xianting, Fu Shen

出版信息

J Biomed Nanotechnol. 2018 Jan 1;14(1):168-178. doi: 10.1166/jbn.2018.2503.

Abstract

Exosomes are nano-vesicles that contribute to the effectiveness of many treatments. The aim of this study was to identify profiles of microRNA (miRNA) contained in serum exosomes that are differentially regulated in patients with prostate cancer undergoing carbon ion radiotherapy (CIRT). RNA was extracted from serum exosomes of eight patients with localized prostate cancer before and after CIRT, and miRNA was analyzed by the next generation sequencing. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis showed that the major signaling pathways associated with the proliferation of prostate cancer cells, such as MAPK, PI3K-AKT, mTOR, and AMPK may be implicated in the mechanism of CIRT action. Notably, 57 miRNAs present in serum exosomes were significantly altered after application of CIRT. A high pre-CIRT expression level of specific miRNAs (miR-493-5p, miR-323a-3p, miR-411-5p, miR-494-3p, miR-379-5p, miR-654-3p, miR-409-3p, miR-543, and miR-200c-3p) predicted therapeutic benefit of CIRT (P < 0.05). Post-CIRT expression of miR-654-3p and miR-379-5p was also associated with CIRT efficacy (P < 0.05). These results suggest that the anti-prostate cancer mechanisms elicited by CIRT at the molecular level may involve exosomal miRNAs. Furthermore, specific miRNAs in serum exosomes, particularly miR-654-3p and miR-379-5p, may serve as promising non-invasive biomarkers predicting efficacy of CIRT for prostate cancer.

摘要

外泌体是有助于多种治疗效果的纳米囊泡。本研究的目的是鉴定接受碳离子放疗(CIRT)的前列腺癌患者血清外泌体中差异调节的微小RNA(miRNA)谱。从8例局限性前列腺癌患者CIRT前后的血清外泌体中提取RNA,并通过下一代测序分析miRNA。京都基因与基因组百科全书(KEGG)通路分析表明,与前列腺癌细胞增殖相关的主要信号通路,如MAPK、PI3K-AKT、mTOR和AMPK,可能参与了CIRT的作用机制。值得注意的是,应用CIRT后,血清外泌体中存在的57种miRNA发生了显著变化。特定miRNA(miR-493-5p、miR-323a-3p、miR-411-5p、miR-494-3p、miR-379-5p、miR-654-3p、miR-409-3p、miR-543和miR-200c-3p)在CIRT前的高表达水平预示着CIRT的治疗益处(P<0.05)。miR-654-3p和miR-379-5p在CIRT后的表达也与CIRT疗效相关(P<0.05)。这些结果表明,CIRT在分子水平上引发的抗前列腺癌机制可能涉及外泌体miRNA。此外,血清外泌体中的特定miRNA,尤其是miR-654-3p和miR-379-5p,可能作为预测CIRT对前列腺癌疗效的有前景的非侵入性生物标志物。

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