Evidence map›Paper›PMID 27323816›Full record

ArticleOncotarget2016

Could gut microbiota serve as prognostic biomarker associated with colorectal cancer patients' survival? A pilot study on relevant mechanism.

Zhiliang Wei, Shougen Cao, Shanglong Liu, Zengwu Yao, Teng Sun, Yi Li, Jiante Li, Dongfeng Zhang, Yanbing Zhou

Abstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed, 9 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

117 citing papers in PubMed, 9 syntheses or guidelines pooled it.

  1. Pooled it
  2. Systematic review: The gut microbiota as a link between colorectal cancer and obesity.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2025
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  9. World journal of gastroenterology · 2017
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  14. Microorganisms · 2026
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57 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Zhiliang WeiDepartment of General Surgery, Affiliated Hospital of Qingdao University, Qingdao, China.
Shougen CaoDepartment of General Surgery, Affiliated Hospital of Qingdao University, Qingdao, China.
Shanglong LiuDepartment of General Surgery, Affiliated Hospital of Qingdao University, Qingdao, China.
Zengwu YaoDepartment of General Surgery, Yantai Yuhuangding Hospital, Yantai, China.
Teng SunDepartment of General Surgery, Qingdao Municipal Hospital Group, Qingdao, China.
Yi LiDepartment of General Surgery, Affiliated Hospital of Qingdao University, Qingdao, China.
Jiante LiDepartment of General Surgery, Affiliated Hospital of Qingdao University, Qingdao, China.
Dongfeng ZhangDepartment of Epidemiology and Health Statistics, Qingdao University Medical College, Qingdao, China.
Yanbing ZhouDepartment of General Surgery, Affiliated Hospital of Qingdao University, Qingdao, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evidences have shown that dysbiosis could promote the progression of colorectal cancer (CRC). However, the association of dysbiosis and prognosis of CRC is barely investigated. Therefore, we used 16S rRNA gene sequencing approach to determine differences in microbiota among tumor tissues of different prognosis and found that Fusobacterium nucleatum and Bacteroides fragilis were more abundant in worse prognosis groups, while Faecalibacterium prausnitzii displayed higher abundance in survival group. To further explore the prognostic value of the found bacteria, Kaplan-Meier and Cox proportional regression analyses were used and the results exhibited that high abundance of F. nucleatum and B. fragilis were independent indicators of poor patient's survival. Besides, the expression of major inflammatory mediator were analyzed using PCR and western blot methods, and it turned out that high abundance of F. nucleatum was associated with increased expression of TNF-α, β-catenin and NF-κB, while COX-2, MMP-9 and NF-κB were positively related with high B. fragilis level, and high level of F. prausnitzii showed lower expression of β-catenin, MMP-9 and NF-κB. Moreover, immunohistochemical analysis indicated that KRAS and BRAF expression were prominent in F. nucleatum and B. fragilis high abundance group, while MLH1 showed lower expression. In conclusion, F. nucleatum, B. fragilis and F. prausnitzii can be identified as useful prognostic biomarkers for CRC, and dysbiosis might worsen the patients' prognosis by up-regulating gut inflammation level.

Indexed as

Gastrointestinal MicrobiomeAdultAgedColorectal NeoplasmsFemaleHumansKaplan-Meier EstimateMaleMiddle AgedPilot ProjectsPrognosisProportional Hazards Modelscolorectal cancerinflammationintestinal microbiologyprognosisprognostic biomarker

Identifiers

PMID27323816
PMCPMC5216788

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.