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解脲脲原体亚种解脲脲原体促进结直肠癌的发展。

Streptococcus gallolyticus subsp. gallolyticus promotes colorectal tumor development.

作者信息

Kumar Ritesh, Herold Jennifer L, Schady Deborah, Davis Jennifer, Kopetz Scott, Martinez-Moczygemba Margarita, Murray Barbara E, Han Fang, Li Yu, Callaway Evelyn, Chapkin Robert S, Dashwood Wan-Mohaiza, Dashwood Roderick H, Berry Tia, Mackenzie Chris, Xu Yi

机构信息

Center for Infectious and Inflammatory Diseases, Institute of Biosciences and Technology, Texas A&M Health Science Center, Houston, Texas, United States of America.

Department of Pathology, Baylor College of Medicine, Houston, Texas, United States of America.

出版信息

PLoS Pathog. 2017 Jul 13;13(7):e1006440. doi: 10.1371/journal.ppat.1006440. eCollection 2017 Jul.

Abstract

Streptococcus gallolyticus subsp. gallolyticus (Sg) has long been known to have a strong association with colorectal cancer (CRC). This knowledge has important clinical implications, and yet little is known about the role of Sg in the development of CRC. Here we demonstrate that Sg promotes human colon cancer cell proliferation in a manner that depends on cell context, bacterial growth phase and direct contact between bacteria and colon cancer cells. In addition, we observed increased level of β-catenin, c-Myc and PCNA in colon cancer cells following incubation with Sg. Knockdown or inhibition of β-catenin abolished the effect of Sg. Furthermore, mice administered with Sg had significantly more tumors, higher tumor burden and dysplasia grade, and increased cell proliferation and β-catenin staining in colonic crypts compared to mice receiving control bacteria. Finally, we showed that Sg is present in the majority of CRC patients and is preferentially associated with tumor compared to normal tissues obtained from CRC patients. These results taken together establish for the first time a tumor-promoting role of Sg that involves specific bacterial and host factors and have important clinical implications.

摘要

解脲脲原体亚种解脲脲原体(Sg)长期以来一直被认为与结直肠癌(CRC)密切相关。这一认识具有重要的临床意义,但关于Sg在CRC发生发展中的作用却知之甚少。在此,我们证明Sg以依赖细胞环境、细菌生长阶段以及细菌与结肠癌细胞直接接触的方式促进人结肠癌细胞增殖。此外,我们观察到与Sg孵育后的结肠癌细胞中β-连环蛋白、c-Myc和增殖细胞核抗原(PCNA)水平升高。β-连环蛋白的敲低或抑制消除了Sg的作用。此外,与接受对照细菌的小鼠相比,给予Sg的小鼠肿瘤明显更多,肿瘤负荷和发育异常分级更高,结肠隐窝中的细胞增殖和β-连环蛋白染色增加。最后,我们表明Sg存在于大多数CRC患者中,与从CRC患者获得的正常组织相比,它优先与肿瘤相关。这些结果共同首次确立了Sg的促肿瘤作用,该作用涉及特定的细菌和宿主因素,并具有重要的临床意义。

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