Evidence map›Paper›PMID 41613792›Full record

ReviewOncology research2026

Cancer-Associated Fibroblasts in Prostate Cancer: Unraveling Mechanisms and Therapeutic Implications.

Yang Wu, Dong Xu, Run Shi, Mingwei Zhan, Shaohui Xu, Xin Wang, Jianpeng Zhang, Zhaokai Zhou, Weizhuo Wang, Yongjie Wang and 3 more

Abstract readReview
In one paragraph

Review in Oncology research, 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

13 authors.

Yang WuThe First Clinical School, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210000, China.
Dong XuThe First Clinical School, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210000, China.
Run ShiThe First Clinical School, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210000, China.
Mingwei ZhanDepartment of Urology, Hangzhou TCM Hospital of Zhejiang Chinese Medical University (Hangzhou Hospital of Traditional Chinese Medicine), Hangzhou, 310007, China.
Shaohui XuInstitute of Functional Nano & Soft Materials (FUNSOM), Soochow University, Suzhou, 215123, China.
Xin WangDepartment of Oncology, Jiangsu Cancer Hospital, Nanjing, 210009, China.
Jianpeng ZhangDepartment of Urology, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, 510030, China.
Zhaokai ZhouDepartment of Urology, The Second Xiangya Hospital of Central South University, Changsha, 410011, China.
Weizhuo WangCenter for Reproductive Medicine, The Second Affiliated Hospital of Soochow University, Suzhou, 215000, China.
Yongjie WangProteomics and Cancer Cell Signaling Group, German Cancer Research Center (DKFZ), Heidelberg, 69120, Germany.
Minglun LiDepartment of Radiation Oncology, Lueneburg Municipal Hospital, Lueneburg, 21339, Germany.
Zihao XuDepartment of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China.
Kaifeng SuThe First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, 250013, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate cancer (PCa) remains a major cause of cancer-related mortality in men, largely due to therapy resistance and metastatic progression. Increasing evidence highlights the tumor microenvironment (TME), particularly cancer-associated fibroblasts (CAFs), as a critical determinant of disease behavior. CAFs constitute a heterogeneous population originating from fibroblasts, mesenchymal stem cells, endothelial cells, epithelial cells undergoing epithelial-mesenchymal transition (EMT), and adipose tissue. Through dynamic crosstalk with tumor, immune, endothelial, and adipocyte compartments, CAFs orchestrate oncogenic processes including tumor proliferation, invasion, immune evasion, extracellular matrix remodeling, angiogenesis, and metabolic reprogramming. This review comprehensively summarizes the cellular origins, phenotypic and functional heterogeneity, and spatial distribution of CAFs within the prostate TME. We further elucidate the molecular mechanisms by which CAFs regulate PCa progression and therapeutic resistance, and critically evaluate emerging strategies to therapeutically target CAF-mediated signaling, metabolic, and immune pathways. By integrating recent advances from single-cell and spatial transcriptomics (ST), our objective is to provide a holistic framework for understanding CAF biology and to highlight potential avenues for stromal reprogramming as an adjunct to current PCa therapies.

Indexed as

Cancer-Associated FibroblastsProstatic NeoplasmsAnimalsEpithelial-Mesenchymal TransitionHumansMaleMetabolic ReprogrammingSignal TransductionTumor Microenvironmentcancer-associated fibroblastsProstate cancertherapy resistancetumor microenvironment

Identifiers

PMID41613792
PMCPMC12848666

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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.