Microbiota Profile and Impact of Fusobacterium nucleatum in Colorectal Cancer Patients of Barretos Cancer Hospital

被引:43
|
作者
de Carvalho, Ana Carolina [1 ]
Pereira, Leandro de Mattos [1 ]
Datorre, Jose Guilherme [1 ]
dos Santos, Wellington [1 ]
Berardinelli, Gustavo Noriz [1 ]
Matsushita, Marcus de Medeiros [2 ]
Oliveira, Marco Antonio [3 ]
Duraes, Ronilson Oliveira [4 ]
Guimaraes, Denise Peixoto [1 ,5 ]
Reis, Rui Manuel [1 ,6 ,7 ]
机构
[1] Barretos Canc Hosp, Mol Oncol Res Ctr, Barretos, Brazil
[2] Barretos Canc Hosp, Dept Pathol, Barretos, Brazil
[3] Barretos Canc Hosp, Epidemiol & Biostat Dept, Barretos, Brazil
[4] Barretos Canc Hosp, Dept Med Oncol, Barretos, Brazil
[5] Barretos Canc Hosp, Dept Prevent, Barretos, Brazil
[6] Univ Minho, Sch Med, Life & Hlth Sci Res Inst ICVS, Braga, Portugal
[7] ICVS 3Bs PT Govt Associate Lab, Braga, Portugal
来源
FRONTIERS IN ONCOLOGY | 2019年 / 9卷
关键词
colorectal cancer; microbiota; Fusobacterium nucleatum; MSI; patient survival; MOLECULAR-FEATURES; GUT MICROBIOME; CARCINOGENESIS; BACTERIA; ASSOCIATION; MORTALITY; IMMUNITY; HEALTH;
D O I
10.3389/fonc.2019.00813
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Microbial diversity has been pointed out as a major factor in the development and progression of colorectal cancer (CRC). We sought to explore the richness and abundance of the microbial community of a series of colorectal tumor samples treated at Barretos Cancer Hospital, Brazil, through 16S rRNA sequencing. The presence and the impact of Fusobacterium nucleatum (Fn) DNA in CRC prognosis was further evaluated by qPCR in a series of 152 CRC cases. An enrichment for potentially oncogenic bacteria in CRC was observed, with Fusobacterium being the most abundant genus in the tumor tissue. In the validation dataset, Fn was detected in 35/152 (23.0%) of fresh-frozen tumor samples and in 6/57 (10.5%) of paired normal adjacent tissue, with higher levels in the tumor (p = 0.0033). Fn DNA in the tumor tissue was significantly associated with proximal tumors (p = 0.001), higher depth of invasion (p = 0.014), higher clinical stages (p = 0.033), poor differentiation (p = 0.011), MSI-positive status (p < 0.0001), BRAF mutated tumors (p < 0.0001), and the loss of expression of mismatch-repair proteins MLH1 (p < 0.0001), MSH2 (p = 0.003), and PMS2 (p < 0.0001). Moreover, the presence of Fn DNA in CRC tissue was also associated with a worse patient cancer-specific survival (69.9 vs. 82.2% in 5 years; p = 0.028) and overall survival (63.5 vs. 76.5%; p = 0.037). Here we report, for the first time, the association of F. nucleatum presence with important clinical and molecular features in a Brazilian cohort of CRC patients. Tumor detection and classification based on the gut microbiome might provide a promising approach to improve the prediction of patient outcome.
引用
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页数:11
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