Evidence map›Paper›PMID 41415548›Full record

ReviewFrontiers in oncology2025

Microbiota-host metabolism reprogramming in colorectal cancer: from pathogenesis to precision therapies.

Chengxu Guo, Caixia Wang

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. 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

2 authors.

Chengxu GuoFeatured Laboratory for Biosynthesis and Target Discovery of Active Components of Traditional Chinese Medicine, School of Traditional Chinese Medicine, Binzhou Medical University, Yantai, China.
Caixia WangFeatured Laboratory for Biosynthesis and Target Discovery of Active Components of Traditional Chinese Medicine, School of Traditional Chinese Medicine, Binzhou Medical University, Yantai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is a highly aggressive malignancy characterized by complex metabolic reprogramming, a hallmark that provides both biosynthetic precursors and signaling molecules to support tumor growth, invasion and therapeutic resistance. A key mechanism underlying this metabolic rewiring is the dynamic interplay between the host and gut microbiota. Gut microbiota derived metabolites, including short-chain fatty acids, secondary bile acids, polyamines and tryptophan derivatives, extensively reshape the CRC metabolic network and modulate the immune microenvironment, thereby influencing tumor progression and therapy response. This review systematically outlines the core features and molecular mechanisms of metabolic reprogramming in CRC, highlights the role of microbiota-host co-metabolism in regulating energy acquisition and immune-metabolic crosstalk, and discusses emerging therapeutic strategies that integrate metabolic targeting and microbiota modulation for precision intervention in CRC.

Indexed as

colorectal cancerimmunometabolismmetabolic reprogrammingmicrobiota-derived metabolitesprecision therapy

Identifiers

PMID41415548
PMCPMC12708274

What OpenQuestion holds

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Registered trials

None linked

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.