Evidence map›Paper›PMID 42120524›Full record

ArticleBritish journal of cancer2026

GDF15 promotes 5-Fluorouracil and Oxaliplatin resistance by promoting stem cell-like phenotype in colorectal cancer.

Masahiro Hashimoto, Shoichiro Urabe, Tsuyoshi Hata, Yoshinao Chinen, Kengo Haruna, Mitsunobu Takeda, Yuki Sekido, Atsushi Hamabe, Takayuki Ogino, Norikatsu Miyoshi and 5 more

Abstract read
In one paragraph

Article in British journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Masahiro Hashimoto *Department of Gastroenterological Surgery, The University of Osaka Graduate School of Medicine, Suita, Japan.
Shoichiro Urabe *Department of Gastroenterological Surgery, The University of Osaka Graduate School of Medicine, Suita, Japan.
Tsuyoshi HataDepartment of Gastroenterological Surgery, The University of Osaka Graduate School of Medicine, Suita, Japan. tsuyoshihata@gesurg.med.osaka-u.ac.jp.ORCID http://orcid.org/0000-0001-6616-9069
Yoshinao ChinenDepartment of Gastroenterological Surgery, The University of Osaka Graduate School of Medicine, Suita, Japan.
Kengo HarunaDepartment of Gastroenterological Surgery, The University of Osaka Graduate School of Medicine, Suita, Japan.
Mitsunobu TakedaDepartment of Gastroenterological Surgery, The University of Osaka Graduate School of Medicine, Suita, Japan.
Yuki SekidoDepartment of Gastroenterological Surgery, The University of Osaka Graduate School of Medicine, Suita, Japan.
Atsushi HamabeDepartment of Gastroenterological Surgery, The University of Osaka Graduate School of Medicine, Suita, Japan.
Takayuki OginoDepartment of Gastroenterological Surgery, The University of Osaka Graduate School of Medicine, Suita, Japan.
Norikatsu MiyoshiDepartment of Gastroenterological Surgery, The University of Osaka Graduate School of Medicine, Suita, Japan.
Taro ToboDepartment of Pathology, Kyushu University Beppu Hospital, Beppu, Japan.
Koshi MimoriDepartment of Surgery, Kyushu University Beppu Hospital, Beppu, Japan.ORCID http://orcid.org/0000-0003-3897-9974
Mamoru UemuraDepartment of Gastroenterological Surgery, The University of Osaka Graduate School of Medicine, Suita, Japan.
Hidetoshi EguchiDepartment of Gastroenterological Surgery, The University of Osaka Graduate School of Medicine, Suita, Japan.
Yuichiro DokiDepartment of Gastroenterological Surgery, The University of Osaka Graduate School of Medicine, Suita, Japan.

Funding

Japan Society for the Promotion of Science London (JSPS London) 25K19762MEXT | Japan Society for the Promotion of Science (JSPS) 25K19762
6 · The paper itself

Abstract

backgroundDespite recent advances in chemotherapy for colorectal cancer (CRC), chemotherapy-sensitive tumours often develop resistance to treatment, which remains a major clinical challenge. This acquired chemoresistance limits the efficacy of subsequent therapies and is associated with a poor prognosis. Therefore, this study identified the mechanisms of acquired chemoresistance in CRC and developed innovative targeted therapies.

methods5-fluorouracil (5-FU)-and oxaliplatin (OX)-resistant CRC cells were established through long-term exposure to anticancer drugs, and RNA sequencing (RNA-seq) was performed. RNA-seq data integrated analysis from resistant cells and public single-cell RNA-seq datasets from clinical CRC samples was conducted to identify key drivers of chemoresistance. Prognostic significance was evaluated by immunohistochemical analysis of liver metastasis specimens from patients with CRC who underwent curative resection of the primary tumours.

resultsChemotherapy exposure enriched high stemness and activated TGF-β signalling. GDF15 was identified as a key molecule upregulated in both chemoresistant and high-stemness cells. Clinically, high GDF15 expression is associated with early recurrence and poor prognosis. Functional assays demonstrated that GDF15 overexpression promoted chemoresistance, stemness, and migratory capacity of CRC cells.

conclusionsGDF15 promotes chemoresistance in CRC by promoting stem cell-like properties. These findings provide insights into therapeutic strategies for overcoming acquired chemoresistance and improving outcomes.

Indexed as

Colorectal NeoplasmsDrug Resistance, NeoplasmFluorouracilGrowth Differentiation Factor 15Neoplastic Stem CellsOxaliplatinAnimalsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansLiver NeoplasmsMaleMicePhenotypePrognosisFluorouracilGDF15 protein, humanGrowth Differentiation Factor 15Oxaliplatin

Identifiers

PMID42120524
PMCPMC13427734

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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.