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配对的激素敏感性和去势抵抗性前列腺癌中肠道微生物群的组成差异

Compositional differences of gut microbiome in matched hormone-sensitive and castration-resistant prostate cancer.

作者信息

Liu Yufei, Jiang Haowen

机构信息

Department of Urology, Huashan Hospital, Fudan University, Shanghai, China.

出版信息

Transl Androl Urol. 2020 Oct;9(5):1937-1944. doi: 10.21037/tau-20-566.

Abstract

BACKGROUND

It is known that gut microbiota can regulate cancer therapies. We hypothesized that gut microbiota may interact with androgen deprivation therapy (ADT) in the process of castration-resistant prostate cancer (CRPC). Here, the differences in gut microbiota between matched hormone-sensitive prostate cancer (HSPC) and CRPC were determined before and after ADT.

METHODS

We profiled the fecal microbiota in matched HSPC and CRPC from 21 patients who received ADT at our urological center using 16S rRNA gene amplicon sequencing. Differences in microbiota were determined with α/β-diversity and LefSe analysis. Functional inference of microbiota was performed with PICRUSt.

RESULTS

The results showed that the gut microbial community in CRPC was significantly altered with increased abundance of several bacterial flora including genus and . For functional analyses, bacterial gene pathways involved in terpenoids/polyketides metabolism and ether lipid metabolism were significantly activated in CRPC.

CONCLUSIONS

Measurable differences in the gut microbiota were identified between HSPC and CRPC. Functional validations are further needed to ascertain the underlying mechanism of these differential microbiota in the process of CRPC, and their potential as new targets to enhance ADT responses.

摘要

背景

已知肠道微生物群可调节癌症治疗。我们假设肠道微生物群可能在去势抵抗性前列腺癌(CRPC)的过程中与雄激素剥夺疗法(ADT)相互作用。在此,我们确定了在ADT前后,配对的激素敏感性前列腺癌(HSPC)和CRPC患者肠道微生物群的差异。

方法

我们使用16S rRNA基因扩增子测序对在我们泌尿外科中心接受ADT的21例患者的配对HSPC和CRPC粪便微生物群进行了分析。通过α/β多样性和LefSe分析确定微生物群的差异。使用PICRUSt对微生物群进行功能推断。

结果

结果显示,CRPC中的肠道微生物群落发生了显著变化,包括属和属在内的几种细菌菌群丰度增加。在功能分析中,参与萜类/聚酮类代谢和醚脂代谢的细菌基因途径在CRPC中被显著激活。

结论

在HSPC和CRPC之间发现了肠道微生物群的可测量差异。进一步需要进行功能验证,以确定这些差异微生物群在CRPC过程中的潜在机制,以及它们作为增强ADT反应新靶点的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9986/7658119/a347940add73/tau-09-05-1937-f1.jpg

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