Raag Agrawal, Sarah Al-Hiyari, Rupert Hugh-White, Robert Hromas, Yash Patel, Elizabeth A Williamson, Mohammed F E Mootor, Alfredo Gonzalez, Jianmin Fu, Roni Haas, Madison Jordan, Brian L Wickes, Ghouse Mohammed, Mao Tian, Molly J Doris, Christian Jobin, Kevin M Wernke, Yu Pan, Takafumi N Yamaguchi, Seth B Herzon, Paul C Boutros, Michael A Liss
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Our aim was to investigate the association of pks<sup>+</sup>E. coli with PC diagnosis and molecular architecture, and its relationship with androgens.</p><p><strong>Methods: </strong>We quantified the association of pks<sup>+</sup>E. coli with PC diagnosis in a volunteer-sampled 235-person cohort from two institutional practices (UT San Antonio). We then used colibactin 742 and DNA/RNA sequencing to evaluate the effects of colibactin 742, dihydrotestosterone (DHT), and their combination in vitro.</p><p><strong>Key findings and limitations: </strong>Colibactin exposure was positively associated with PC diagnosis (p = 0.04) in our clinical cohort, and significantly increased replication fork stalling and fusions in vitro (p < 0.01). Combined in vitro exposure to colibactin 742 and DHT induced more somatic mutations of all types than exposure to either alone. The combination also elicited kataegis, with a higher density of somatic point mutations. Laboratory analyses were conducted using a single cell line, which limited our ability to fully recapitulate the complexity of PC etiology.</p><p><strong>Conclusions and clinical implications: </strong>Our findings are consistent with synergistic induction of genome instability and kataegis by colibactin 742 and DHT in cell culture. Colibactin-producing pks<sup>+</sup> E. coli may plausibly contribute to PC etiology.</p><p><strong>Patient summary: </strong>We investigated whether a bacterial toxin that is linked to colon cancer can also cause prostate cancer. Our results support this idea by showing a link between the toxin and prostate cancer diagnosis in a large patient population. 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Combined in vitro exposure to colibactin 742 and DHT induced more somatic mutations of all types than exposure to either alone. The combination also elicited kataegis, with a higher density of somatic point mutations. Laboratory analyses were conducted using a single cell line, which limited our ability to fully recapitulate the complexity of PC etiology.</p><p><strong>Conclusions and clinical implications: </strong>Our findings are consistent with synergistic induction of genome instability and kataegis by colibactin 742 and DHT in cell culture. Colibactin-producing pks<sup>+</sup> E. coli may plausibly contribute to PC etiology.</p><p><strong>Patient summary: </strong>We investigated whether a bacterial toxin that is linked to colon cancer can also cause prostate cancer. Our results support this idea by showing a link between the toxin and prostate cancer diagnosis in a large patient population. 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引用次数: 0
摘要
背景和目的:前列腺癌(PC)的病因是多因素的,目前尚不清楚。有人认为,致病性岛 pks(pks+)阳性的产大肠杆菌通过诱导基因组不稳定性引发癌症。在 PC 中,雄激素会促进致癌易位。我们的目的是研究 pks+ 大肠杆菌与 PC 诊断和分子结构的关联及其与雄激素的关系:方法:我们从两家机构(UT 圣安东尼奥)的 235 人队列中对 pks+E. coli 与 PC 诊断的相关性进行了量化。然后,我们使用 colibactin 742 和 DNA/RNA 测序来评估 colibactin 742、双氢睾酮 (DHT) 及其组合在体外的影响:在我们的临床队列中,高立克次素暴露与 PC 诊断呈正相关(p = 0.04),并显著增加了体外复制叉停滞和融合(p 结论和临床意义:我们的研究结果表明,在细胞培养过程中,可乐菌素 742 和 DHT 可协同诱导基因组不稳定性和卡他性。患者总结:我们研究了一种与结肠癌有关的细菌毒素是否也会导致前列腺癌。我们的研究结果表明,在大量患者中,该毒素与前列腺癌诊断之间存在联系,从而支持了这一观点。我们还发现,当这种毒素与睾酮结合时,会导致前列腺癌细胞的基因功能紊乱。
Colibactin Exerts Androgen-dependent and -independent Effects on Prostate Cancer.
Background and objective: The etiology of prostate cancer (PC) is multifactorial and poorly understood. It has been suggested that colibactin-producing Escherichia coli positive for the pathogenicity island pks (pks+) initiate cancers via induction of genomic instability. In PC, androgens promote oncogenic translocations. Our aim was to investigate the association of pks+E. coli with PC diagnosis and molecular architecture, and its relationship with androgens.
Methods: We quantified the association of pks+E. coli with PC diagnosis in a volunteer-sampled 235-person cohort from two institutional practices (UT San Antonio). We then used colibactin 742 and DNA/RNA sequencing to evaluate the effects of colibactin 742, dihydrotestosterone (DHT), and their combination in vitro.
Key findings and limitations: Colibactin exposure was positively associated with PC diagnosis (p = 0.04) in our clinical cohort, and significantly increased replication fork stalling and fusions in vitro (p < 0.01). Combined in vitro exposure to colibactin 742 and DHT induced more somatic mutations of all types than exposure to either alone. The combination also elicited kataegis, with a higher density of somatic point mutations. Laboratory analyses were conducted using a single cell line, which limited our ability to fully recapitulate the complexity of PC etiology.
Conclusions and clinical implications: Our findings are consistent with synergistic induction of genome instability and kataegis by colibactin 742 and DHT in cell culture. Colibactin-producing pks+ E. coli may plausibly contribute to PC etiology.
Patient summary: We investigated whether a bacterial toxin that is linked to colon cancer can also cause prostate cancer. Our results support this idea by showing a link between the toxin and prostate cancer diagnosis in a large patient population. We also found that this toxin causes genetic dysfunction in prostate cancer cells when combined with testosterone.
期刊介绍:
Journal Name: European Urology Oncology
Affiliation: Official Journal of the European Association of Urology
Focus:
First official publication of the EAU fully devoted to the study of genitourinary malignancies
Aims to deliver high-quality research
Content:
Includes original articles, opinion piece editorials, and invited reviews
Covers clinical, basic, and translational research
Publication Frequency: Six times a year in electronic format