Evidence map›Paper›PMID 40849307›Full record

ArticleCell death discovery2025

One-carbon metabolic pathway is a novel molecular signature for CD44-positive intestinal-type gastric cancer.

Seyeon Joo, Yoojin Bae, Bo Kyung Yoon, Yeonjin Je, Yuna Kim, Minki Kim, Su-Jin Shin, Sungsoon Fang, Jie-Hyun Kim

Abstract read
In one paragraph

Article in Cell death discovery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. 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

9 authors.

Seyeon Joo *Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul, South Korea.ORCID http://orcid.org/0000-0003-3522-8323
Yoojin Bae *Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Bo Kyung YoonDepartment of Microbiology and Immunology, Yonsei University College of Medicine, Seoul, South Korea.
Yeonjin JeDepartment of Medicine, Yonsei University College of Medicine, Seoul, South Korea.
Yuna KimDepartment of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Minki KimGraduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul, South Korea.ORCID http://orcid.org/0000-0002-5587-9935
Su-Jin ShinDepartment of Pathology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea. CHARM@yuhs.ac.ORCID http://orcid.org/0000-0001-9114-8438
Sungsoon FangGraduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul, South Korea. SFANG@yuhs.ac.ORCID http://orcid.org/0000-0003-0201-5567
Jie-Hyun KimDepartment of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea. OTILIA94@yuhs.ac.ORCID http://orcid.org/0000-0002-9198-3326

Funding

Ministry of Health and Welfare (Ministry of Health, Welfare and Family Affairs) HR18C001202National Research Foundation of Korea (NRF) NRF-2021R1A2C2011296Yonsei University | Yonsei University College of Medicine (YUCM) 6-2024-0105
6 · The paper itself

Abstract

Intratumoral heterogeneity (ITH), arising from various factors, plays a crucial role in diverse cancers, yet research on ITH remains in its early stages. To explore this phenomenon further, we conducted single-nuclei transcriptome profiling on patient-derived organoids (PDOs) from two histologically pure subtypes of gastric cancer. We identified differences in cancer stem cell marker expression among intestinal-type samples and their correlation with one-carbon (1C) metabolism. Notably, some gastric cancer samples, although histologically classified as intestinal-type, exhibited diffuse-like genetic characteristics. This finding suggests the potential for employing a 1C metabolism inhibition strategy as a therapeutic approach for these genetically diffuse-like gastric cancers. This study highlights the necessity of addressing ITH in PDO-based preclinical models and contributes valuable insights toward advancing precision medicine treatments for gastric cancer.

Identifiers

PMID40849307
PMCPMC12375131

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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.