Evidence map›Paper›PMID 38189541›Full record

ArticleBriefings in bioinformatics2023

Specific network information gain for detecting the critical state of colorectal cancer based on gut microbiome.

Xueqing Peng, Rong Gao, Jing Ren, Jianbo Lu, Xu Ma, Peiluan Li

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Antioxidant Role of Probiotics in Inflammation-Induced Colorectal Cancer.International journal of molecular sciences · 2024
    Review
  4. Article
  5. 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

6 authors.

Xueqing PengSchool of Mathematics and Statistics, Henan University of Science and Technology, Luoyang, China.
Rong GaoBig Data Institute, Central South University, Changsha, China.
Jing RenSchool of Mathematics and Statistics, Henan University of Science and Technology, Luoyang, China.
Jianbo LuNational Human Genetics Resource Center, National Research Institute for Family Planning, Beijing 100081, China.
Xu MaNational Human Genetics Resource Center, National Research Institute for Family Planning, Beijing 100081, China.
Peiluan LiSchool of Mathematics and Statistics, Henan University of Science and Technology, Luoyang 471023, China.ORCID 0000-0001-5545-6185

Funding

Key R & D, Promotion Special Program of Henan Province 212102310988Major projects of Henan Province 231100220100National Natural Science Foundation of China 61673008Young Backbone Teacher Funding Scheme of Henan 2019GGJS079
6 · The paper itself

Abstract

There generally exists a critical state or tipping point from a stable state to another in the development of colorectal cancer (CRC) beyond which a significant qualitative transition occurs. Gut microbiome sequencing data can be collected non-invasively from fecal samples, making it more convenient to obtain. Furthermore, intestinal microbiome sequencing data contain phylogenetic information at various levels, which can be used to reliably identify critical states, thereby providing early warning signals more accurately and effectively. Yet, pinpointing the critical states using gut microbiome data presents a formidable challenge due to the high dimension and strong noise of gut microbiome data. To address this challenge, we introduce a novel approach termed the specific network information gain (SNIG) method to detect CRC's critical states at various taxonomic levels via gut microbiome data. The numerical simulation indicates that the SNIG method is robust under different noise levels and that it is also superior to the existing methods on detecting the critical states. Moreover, utilizing SNIG on two real CRC datasets enabled us to discern the critical states preceding deterioration and to successfully identify their associated dynamic network biomarkers at different taxonomic levels. Notably, we discovered certain 'dark species' and pathways intimately linked to CRC progression. In addition, we accurately detected the tipping points on an individual dataset of type I diabetes.

Indexed as

Colorectal NeoplasmsDiabetes Mellitus, Type 1Gastrointestinal MicrobiomeComputer SimulationHumansPhylogenycritical statedynamic network biomarkers (DNBs)gut microbiome datainformation gainspecific network information gain (SNIG)

Identifiers

PMID38189541
PMCPMC10772986

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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.