PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
April 5, 2026Cancer Research0 citations

Abstract 2098: CNTF governs exercise-induced myofibroblast reversion in prostate cancer.

View Full Paper
PGPengju GongYLYuan LiuIndiana University HealthLHLeng HanUniversity of Indianapolis

Key Points

  • The study aims to investigate the molecular mechanisms by which exercise influences myofibroblast dynamics in prostate cancer.
  • Utilized the Transgenic Adenocarcinoma of the Mouse Prostate (TRAMP) model.
  • Conducted single-cell RNA-seq and spatial analyses of tumors.
  • Administered recombinant CNTF to evaluate its effects on tumor growth and immune response.
  • Long-term moderate exercise suppressed primary tumor growth and metastasis.
  • Exercise reversed myofibroblast transition to a resting phenotype.
  • CNTF was identified as a cytokine mediating these effects and enhancing CD8+ T-cell infiltration.
  • Recombinant CNTF suppressed tumor growth in vivo and worked synergistically with immune checkpoint blockade.

Abstract

Abstract Prostate cancer (PCa) remains a major cause of cancer-related morbidity and mortality in the United States, with more than 2.5 million new cases reported annually. Epidemiological studies suggest that physical exercise reduces PCa risk and progression, yet the underlying molecular and stromal mechanisms remain poorly defined. Here, we demonstrate that long-term and moderate exercise significantly suppresses primary tumor growth and metastatic spread in the Transgenic Adenocarcinoma of the Mouse Prostate (TRAMP) model. Single-cell RNA-seq and spatial analyses of the tumor microenvironment (TME) revealed an abundance of myofibroblast populations in PCa, a hallmark associated with tumor progression and immunosuppression. Exercise robustly reversed this myofibroblast transition, shifting fibroblasts toward a resting phenotype in the TRAMP model. Mechanistically, we identified ciliary neurotrophic factor (CNTF) as an exercise-induced cytokine that restrains myofibroblast transition and enhances CD8+ T-cell infiltration within the TME. This CNTF-dependent remodeling of the TME emerged as a key determinant of the anti-tumor effects of exercise. Therapeutically, recombinant CNTF suppressed PCa tumor growth in vivo and demonstrated synergy with immune checkpoint blockade, suggesting that CNTF restoration provides a promising strategy to sensitize PCa to immunotherapy. Collectively, our findings reveal a previously unrecognized CNTF-mediated axis that links physical exercise to fibroblast plasticity and anti-tumor immunity in PCa. This work also provides critical insights into mitigating potential risk factors for PCa patient survival outcomes, offering an avenue for further studies that may serve as a foundation for future clinical considerations for patients with this cancer type. Citation Format: Pengju Gong, Yuan Liu, Leng Han, Liuqing Yang, Chunru Lin. CNTF governs exercise-induced myofibroblast reversion in prostate cancer abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2098.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Gong et al. (2026) studied this question.

synapsesocial.com/papers/69d1fdb0a79560c99a0a3d56https://doi.org/10.1158/1538-7445.am2026-2098
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Abstract 298: Contribution of cancer associated fibroblasts to treatment response and resistance in high-risk multifocal prostate cancer2024 · 2 citations
  2. 2Abstract 7419: Comprehensive profiling of primary and metastatic prostate tumors reveals distinct tumor and fibroblast cell states associated with androgen resistance2026
  3. 3Abstract 166: Rewiring the dendritic cell: Regulatory T cell axis sensitizes prostate cancer to immunotherapy.2026
  4. 4Abstract LB319: Klf5 acetylation remodels tumor microenvironment to constrain PTEN-deficient prostate tumor growth2024
  5. 5Abstract 1585: Tenascin C in pancreatic cancer-associated fibroblasts enhances epithelial mesenchymal transition and is associated with resistance to immune checkpoint inhibitor2024 · 1 citations