Evidence map›Paper›PMID 40693233›Full record

ReviewJournal of the National Cancer Center2025

Overcoming cancer treatment resistance: Unraveling the role of cancer-associated fibroblasts.

Xiaoyuan Wang, Yinuo Zhou, Yingzhuo Wang, Jiaxin Yang, Zhengqian Li, Fuliang Liu, Anni Wang, Zhenhao Gao, Chen Wu, Hang Yin

Abstract readReview
In one paragraph

Review in Journal of the National Cancer Center, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

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

  1. Pooled it
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  10. Integrating multi-omics data for next-generation cancer research and precision medicine.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  11. Review
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  14. Cancer-associated fibroblasts as a potential therapeutic target for thyroid cancers.International journal of surgery (London, England) · 2026
    Review
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  18. Targeting tumor transition windows.Exploration of targeted anti-tumor therapy · 2026
    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

10 authors.

Xiaoyuan WangDepartment of Thoracic Surgery, Harbin Medical University Cancer Hospital, Harbin, China.
Yinuo ZhouDepartment of Radiation Therapy, Harbin Medical University Cancer Hospital, Harbin, China.
Yingzhuo WangDepartment of Radiation Therapy, Harbin Medical University Cancer Hospital, Harbin, China.
Jiaxin YangDepartment of Thoracic Surgery, Harbin Medical University Cancer Hospital, Harbin, China.
Zhengqian LiDepartment of Thoracic Surgery, Harbin Medical University Cancer Hospital, Harbin, China.
Fuliang LiuDepartment of Radiation Therapy, Harbin Medical University Cancer Hospital, Harbin, China.
Anni WangDepartment of Radiation Therapy, Harbin Medical University Cancer Hospital, Harbin, China.
Zhenhao GaoDepartment of Radiation Therapy, Harbin Medical University Cancer Hospital, Harbin, China.
Chen WuDepartment of Etiology and Carcinogenesis, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Hang YinDepartment of Radiation Therapy, Harbin Medical University Cancer Hospital, Harbin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The resistance to cancer treatment is a major clinical obstacle, being strongly influenced by the tumor microenvironment (TME). Cancer-associated fibroblasts (CAFs) are critical elements of the TME. CAFs are heterogeneous and are activated through diverse pathways. These CAFs engage in reciprocal interactions with tumor cells, driving tumor progression and therapeutic resistance. In this review, we discuss the role of CAFs in the development of tumor resistance to chemotherapy, radiotherapy, targeted therapy, and immunotherapy. Besides, we summarize recent clinical trials in CAF-targeted therapies. The development of resistance involves physical barrier formation, metabolic reprogramming, exosome release, DNA repair, bypass pathway activation, multidrug resistance protein upregulation, and immune checkpoint inhibition. Challenges remain in addressing drug resistance despite the therapeutic potential of targeting CAFs: the cellular origins of CAFs need to be clarified, and their limited clinical applications need to be increased. Future studies should focus on elucidating the reasons for CAF heterogeneity, developing precise targeting strategies, and validating the clinical safety and efficacy of CAF-based therapies to overcome treatment resistance and improve patient outcomes.

Indexed as

Cancer-associated fibroblastsCancer treatment resistanceImmune suppressionSignaling pathwaysTumor microenvironment

Identifiers

PMID40693233
PMCPMC12276570

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.