Evidence map›Paper›PMID 41446733›Full record

ArticleiScience2025

Intratumoral microbiota-derived S1P sensitizes the combination therapy of capecitabine and PD-1 inhibitors.

Chen-Shu Dai, Tian-Tian Qi, Hui-Ling Shang, Ri-Hua Xie, Hao Liu, Zhen-Ming Liu, Yi-Min Cui, Yu-Hang Zhang

Abstract read
In one paragraph

Article in iScience, 2025. 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. Review
  3. 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

8 authors.

Chen-Shu DaiInstitute of Clinical Pharmacology, Peking University First Hospital, Beijing 100191, China.
Tian-Tian QiInstitute of Clinical Pharmacology, Peking University First Hospital, Beijing 100191, China.
Hui-Ling ShangDepartment of Nursing, Affiliated Foshan Maternity & Child Healthcare Hospital, Southern Medical University, Foshan 528100, China.
Ri-Hua XieDepartment of Nursing, Affiliated Foshan Maternity & Child Healthcare Hospital, Southern Medical University, Foshan 528100, China.
Hao LiuDepartment of Nursing, Affiliated Foshan Maternity & Child Healthcare Hospital, Southern Medical University, Foshan 528100, China.
Zhen-Ming LiuState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
Yi-Min CuiInstitute of Clinical Pharmacology, Peking University First Hospital, Beijing 100191, China.
Yu-Hang ZhangInstitute of Clinical Pharmacology, Peking University First Hospital, Beijing 100191, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clinical responses of colorectal cancer (CRC) treatments vary considerably due to the heterogeneity of tumor microenvironment (TME), where intratumoral microbiota may reshape the unique inflammation imprints. However, its complex mechanistic underpinnings remain incompletely elucidated. Herein, we sought to delineate the critical role of intratumoral microbiota in potentiating combination therapeutics against CRC. By comparing germ-free (GF) and specific pathogen-free (SPF) mouse models of 33 potential CRC treatments, we screened out capecitabine-MIH4 (anti-PD-1 antibody) combination regimen significantly augmented by intratumoral microbiota in tumor regression. The enrichment of enterotoxigenic

Indexed as

Biological sciencesCancerImmunologyMicrobiome

Identifiers

PMID41446733
PMCPMC12723371

What OpenQuestion holds

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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.