Evidence map›Paper›PMID 40567024›Full record

ArticleCancer medicine2025

Influence of Citrobacter freundii on NINJ2 Expression and Oxaliplatin Resistance in Colorectal Cancer.

Reio Ueta, Hiroo Imai, Ken Saijo, Yoshifumi Kawamura, Shuto Kodera, Chikashi Ishioka

Abstract read
In one paragraph

Article in Cancer medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

  1. Review
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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.

Reio UetaDepartment of Clinical Oncology, Tohoku University Graduate School of Medicine, Sendai, Japan.ORCID https://orcid.org/0009-0008-9429-3209
Hiroo ImaiDepartment of Clinical Oncology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Ken SaijoDepartment of Clinical Oncology, Tohoku University Graduate School of Medicine, Sendai, Japan.ORCID https://orcid.org/0000-0003-0179-3789
Yoshifumi KawamuraDepartment of Clinical Oncology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Shuto KoderaDepartment of Clinical Oncology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Chikashi IshiokaDepartment of Clinical Oncology, Tohoku University Graduate School of Medicine, Sendai, Japan.ORCID https://orcid.org/0000-0002-3023-1227

Funding

Japan Society for the Promotion of Science JP22K07293
6 · The paper itself

Abstract

backgroundOxaliplatin, a third-generation platinum-based chemotherapeutic agent, is widely used in the treatment of colorectal cancer (CRC). However, some patients do not respond effectively to oxaliplatin, and intrinsic resistance to the drug poses a significant challenge. Recent studies have revealed an association between the gut microbiome and the progression of CRC. We hypothesized that Citrobacter freundii, a component of the gut microbiome, contributes to oxaliplatin resistance by regulating specific gene expression in CRC cells.

methodsA bacterial culture filtrate from Citrobacter freundii was employed in the experiments. The CRC cell line RKO, following exposure to this filtrate, was analyzed using high-throughput RNA sequencing. Candidate genes were identified through MTT assays, siRNA knockdown, and overexpression experiments. Apoptosis and reactive oxygen species (ROS) assays were performed to investigate the underlying mechanisms. Finally, a xenograft mouse model was used to evaluate oxaliplatin resistance in vivo.

resultsExposure to bacterial culture filtrate from Citrobacter freundii induced oxaliplatin resistance in RKO cells with downregulation of the NINJ2 gene as a possible molecular mechanism. ReducedNINJ2 gene expression suppressed oxaliplatin-induced apoptosis and ROS generation. A tendency toward reduced oxaliplatin efficacy was observed in vivo when NINJ2 gene expression was suppressed.

conclusionThis study demonstrates that Citrobacter freundii promotes oxaliplatin resistance in CRC through downregulation of NINJ2 gene. NINJ2 gene may serve as a predictive biomarker and therapeutic target to overcome oxaliplatin resistance in CRC.

Indexed as

Antineoplastic AgentsCitrobacter freundiiColorectal NeoplasmsDrug Resistance, NeoplasmOxaliplatinAnimalsApoptosisCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansMiceMice, Inbred BALB CMice, NudeReactive Oxygen SpeciesXenograft Model Antitumor AssaysAntineoplastic AgentsOxaliplatinReactive Oxygen Speciesbacterial culture filtrateCitrobacter freundiicolon cancergut microbiomeoxaliplatin

Identifiers

PMID40567024
PMCPMC12198655

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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.