Evidence map›Paper›PMID 40664751›Full record

ArticleCommunications biology2025

Exo-miR-1911-5p regulates ferroptosis to promote macrophages M2 polarization-mediated gastric cancer cisplatin resistance via MYB/AKR1B10/ACC.

Zihao Kong, Min Zhang, Hui Yuan, Jiahao Liu, Huaiming Sang, Ping Zhao, Miao Xu, Chuanlong Zhu, Guoxin Zhang

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

9 authors.

Zihao Kong *Department of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.ORCID http://orcid.org/0000-0003-1693-9250
Min Zhang *Department of Gastroenterology, The Affiliated Hospital of Yangzhou University, Yangzhou, China.
Hui Yuan *Department of Infectious Disease, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Jiahao Liu *Department of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Huaiming SangDepartment of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Ping ZhaoDepartment of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Miao XuDepartment of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Chuanlong ZhuDepartment of Infectious Disease, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China. zhucl@njmu.edu.cn.ORCID http://orcid.org/0000-0002-0657-828X
Guoxin ZhangDepartment of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China. guoxinz@njmu.edu.cn.ORCID http://orcid.org/0000-0002-7531-0404

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor-associated macrophages (TAMs) have been implicated in fostering various hallmarks of cancer progression in gastric cancer (GC). However, the intricate molecular mechanisms underlying TAM-induced chemoresistance remain incompletely understood. Exosomes emerge as key players, mediating TAM-induced resistance to cisplatin (DDP) by regulating ferroptosis. Our investigation reveals that exo-miR-1911-5p, delivered to GC cells from TAMs, significantly contributes to cisplatin resistance. Specifically, direct modulation of MYB by MiR-1911-5p leads to decreased expression of AKR1B10, a crucial factor in preventing ferroptosis. Further exploration confirms the regulation of ACC by AKR1B10. Through targeting the MYB/AKR1B10/ACC axis, exo-miR-1911-5p inhibits ferroptosis to enhances cisplatin resistance. Additionally, exo-miR-1911-5p promotes M2 polarization of TAMs by targeting ARHGEF3. Collectively, our findings highlight the critical role of exo-miR-1911-5p in mediating cisplatin resistance through modulating the cross-talk between TAMs and GC. Targeting exo-miR-1911-5p could represent a promising strategy for overcoming DDP resistance in GC.

Indexed as

CisplatinDrug Resistance, NeoplasmFerroptosisMacrophagesMicroRNAsProto-Oncogene Proteins c-mybStomach NeoplasmsTumor-Associated MacrophagesAnimalsAntineoplastic AgentsCell Line, TumorExosomesGene Expression Regulation, NeoplasticHumansMiceAntineoplastic AgentsCisplatinMicroRNAsMYB protein, humanProto-Oncogene Proteins c-myb

Identifiers

PMID40664751
PMCPMC12263902

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.