Evidence map›Paper›PMID 27880935›Full record

ArticleOncotarget2017

Evolutionary biologic changes of gut microbiota in an 'adenoma-carcinoma sequence' mouse colorectal cancer model induced by 1, 2-Dimethylhydrazine.

Teng Sun, Shanglong Liu, Yanbing Zhou, Zengwu Yao, Dongfeng Zhang, Shougen Cao, Zhiliang Wei, Bin Tan, Yi Li, Zheng Lian and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
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

31 citing papers in PubMed, 55 citations in OpenAlex.

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  16. Faecal microbial biomarkers in early diagnosis of colorectal cancer.Journal of cellular and molecular medicine · 2021
    Review
  17. Article
  18. NFnetFu: A novel workflow for microbiome data fusion.Computers in biology and medicine · 2021
    Article
  19. Article
  20. Review
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

11 authors at 4 institutions in 1 country.

Teng SunDepartment of General Surgery, Qingdao municipal hospital, Qingdao, China.
Shanglong LiuDepartment of General Surgery, Affiliated Hospital of Qingdao University, Qingdao, China.
Yanbing ZhouDepartment of General Surgery, Affiliated Hospital of Qingdao University, Qingdao, China.
Zengwu YaoDepartment of General Surgery, Yantai Yuhuangding Hospital, Yantai, China.
Dongfeng ZhangDepartment of Epidemiology and Health Statistics, Qingdao University Medical College, Qingdao, China.
Shougen CaoDepartment of General Surgery, Affiliated Hospital of Qingdao University, Qingdao, China.
Zhiliang WeiDepartment of General Surgery, Affiliated Hospital of Qingdao University, Qingdao, China.
Bin TanDepartment of General Surgery, Affiliated Hospital of Qingdao University, Qingdao, China.
Yi LiDepartment of General Surgery, Affiliated Hospital of Qingdao University, Qingdao, China.
Zheng LianDepartment of General Surgery, Zhucheng People's Hospital, Weifang, China.
Song WangDepartment of General Surgery, Linzi District People's Hospital, Zibo, China.
Qingdao University · CNAffiliated Hospital of Qingdao University · CNLinzi District People's Hospital · CNYuhuangding Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The molecular biological mechanisms underlying the evolutionary biologic changes leading to carcinogenesis remain unclear. The main objective of our study was to explore the evolution of the microbiota community and molecules related with CRC in the dynamic transition from normal colon epithelium to premalignant adenoma with the aid of an 'adenoma-carcinoma sequence' mouse CRC model induced by DMH. We generated a modified mouse CRC model induced by DMH for DNA sequences, and characterized the molecular networks. Data from 454 pyrosequencing of the V3- V5 region of the 16S rDNA gene and immunohistochemical detection of APC, P53, K-RAS and BRAF genes were assessed with Principal coordinates, UniFrac, and Kruskal-Wallis rank sum test. The inflammatory group showed enrichment of Bacteroidetes and Porphyromonadaceae (P < 0.01). OTUs affiliated with Firmicutes were enriched in the hyperproliferative group (P < 0.01). Rikenellaceae and Ruminococcaceae showed an increasing trend during the CRC process while the opposite pattern was observed for Prevotellaceaeand Enterobacteriaceae. OTUs related to Alistipes finegoldii were significantly increased during CRC development, P53, K-RAS and BRAF, were gradually increased (P < 0.05). Conversely, expression of APC was decreased during the course of development of CRC. Our results demonstrate that the biological evolutionary shift of gut microbiota, characterized by a gradual decrease in 'driver' bacteria and an increase in DNA damage-causing bacteria, is accompanied by tumor development in the CRC model. The synergistic actions of microbiota dysbiosis and effects of bacterial metabolites on related molecular events are proposed to contribute to the progression of CRC tumorigenesis.

Indexed as

Cell Transformation, Neoplastic1,2-DimethylhydrazineAdenocarcinomaAdenomaAdenomatous Polyposis Coli ProteinAnimalsBacteriaCarcinogenesisColonColorectal NeoplasmsDisease ProgressionDNA, BacterialDNA DamageDysbiosisGastrointestinal MicrobiomeImmunohistochemistry1,2-DimethylhydrazineAdenomatous Polyposis Coli Proteinadenomatous polyposis coli protein, mouseBraf protein, mouseDNA, BacterialHras protein, mouseProto-Oncogene Proteins B-rafProto-Oncogene Proteins p21(ras)RNA, BacterialRNA, Ribosomal, 16STumor Suppressor Protein p53animal modelcolorectal cancermicrobiology

Identifiers

PMID27880935
PMCPMC5352133
OpenAlexW2556082987

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.