Streptococcus gallolyticus subsp gallolyticus promotes colorectal tumor development

被引:168
作者
Kumar, Ritesh [1 ]
Herold, Jennifer L. [1 ]
Schady, Deborah [2 ]
Davis, Jennifer [3 ,4 ]
Kopetz, Scott [3 ]
Martinez-Moczygemba, Margarita [1 ]
Murray, Barbara E. [5 ,6 ]
Han, Fang [7 ]
Li, Yu [7 ]
Callaway, Evelyn [8 ]
Chapkin, Robert S. [8 ]
Dashwood, Wan-Mohaiza [9 ]
Dashwood, Roderick H. [9 ]
Berry, Tia [10 ]
Mackenzie, Chris [6 ]
Xu, Yi [1 ,6 ,11 ]
机构
[1] Texas A&M Hlth Sci Ctr, Ctr Infect & Inflammatory Dis, Inst Biosci & Technol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Pathol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Epidemiol, Houston, TX 77030 USA
[5] Univ Texas Hlth Sci Ctr Houston, Dept Internal Med, Houston, TX 77030 USA
[6] Univ Texas Hlth Sci Ctr Houston, Dept Microbiol & Microbial Genet, Houston, TX 77030 USA
[7] Harbin Inst Technol, Harbin, Heilongjiang, Peoples R China
[8] Texas A&M Univ, Program Integrat Nutr & Complex Dis, College Stn, TX USA
[9] Texas A&M Hlth Sci Ctr, Ctr Epigenet & Dis Prevent, Inst Biosci & Technol, Houston, TX USA
[10] Texas A&M Hlth Sci Ctr, Ctr Translat Canc Res, Inst Biosci & Technol, Houston, TX USA
[11] Texas A&M Hlth Sci Ctr, Dept Microbial Pathogenesis & Immunol, Coll Med, College Stn, TX 77843 USA
关键词
HELICOBACTER-PYLORI; BETA-CATENIN; COLON-CANCER; FUSOBACTERIUM-NUCLEATUM; INTESTINAL TUMORIGENESIS; SIGNALING PATHWAY; INFECTIOUS AGENTS; EPITHELIAL-CELLS; BOVIS BACTEREMIA; E-CADHERIN;
D O I
10.1371/journal.ppat.1006440
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 beta-catenin, c-Myc and PCNA in colon cancer cells following incubation with Sg. Knockdown or inhibition of beta-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 beta-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.
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页数:31
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