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Background: Cancer-associated fibroblasts (CAFs) are the most important cellular components in bladder urothelial carcinoma (BLCA) and are involved in the development and immunosuppression of BLCA. Therefore, we aimed to construct a CAF-associated signature for predicting the prognosis and immunotherapy response in patients with BLCA.
Methods: CAF infiltration and stromal score were quantified using two algorithms. Weighted gene co-expression network analysis (WGCNA) was performed to identify the CAF-associated modules and hub genes. Univariate Cox and Least Absolute Shrinkage and Selection Operator regression analyses were used for constructing CAF signatures and calculating CAF scores. The ability of the CAF signature to predict prognosis and response to immunotherapy was validated using the data from three cohorts.
Results: WGCNA identified two CAF-associated modules and constructed a CAF signature containing 27 genes. In all three cohorts, patients with high CAF scores had markedly worse prognoses than those with low CAF scores, and CAF scores were independent risk factors. In addition, patients with high CAF scores did not respond to immunotherapy, whereas those with lower CAF scores responded to immunotherapy.
Conclusion: CAF signature can be used to predict prognosis and immunotherapy response to guide individualized treatment planning in patients with BLCA.
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http://dx.doi.org/10.1080/13685538.2023.2233609 | DOI Listing |
Clin Oral Investig
September 2025
Department of Innovative Technologies in Medicine & Dentistry, "G. D'Annunzio" University, Via Dei Vestini 31, Chieti, Italy.
Objectives: This study aimed to compare the efficacy of the full-thickness palatal graft technique (FTPGT) and the coronally advanced flap with subepithelial connective tissue graft (CAF + SCTG) in achieving complete root coverage (CRC) in single gingival recessions (GR).
Methods: Forty healthy patients with a single RT1 GR were randomized into two groups: 20 treated with CAF + SCTG and 20 with FTPGT. Baseline and 12-month measurements of GR, keratinized tissue width (KTW), probing depth (PD), clinical attachment level (CAL), and gingival thickness (GT) were recorded.
Front Immunol
September 2025
Wound Healing Center, Peking University Third Hospital, Beijing, China.
Background And Objective: Melanoma exhibits profound biological complexity, driven by immune evasion, phenotypic plasticity, and resistance to therapy. While programmed cell death (PCD) shapes tumor-immune interactions, its mechanistic landscape in melanoma remains incompletely defined. This study aims to comprehensively characterize PCD-related signatures and their associations with tumor heterogeneity, prognosis, and immunotherapeutic outcomes.
View Article and Find Full Text PDFJ Pathol
September 2025
Department of Acupuncture and Moxibustion, Shenzhen Bao'an Traditional Chinese Medicine Hospital, Shenzhen, PR China.
Breast cancer progression is profoundly influenced by interactions within the tumor microenvironment, particularly between cancer-associated fibroblasts and immune cells. This study investigated how cancer-associated fibroblasts impact immune cells in the context of high-fat diets, focusing on key genes involved in these interactions. By analyzing breast cancer-related single-cell and bulk RNA sequencing data, we identified candidate genes in cancer-associated fibroblasts that influence immune cell behavior.
View Article and Find Full Text PDFHereditas
August 2025
Department of Neurosurgery, Tianjin Medical University General Hospital, Tianjin, 300000, China.
Cancer-associated fibroblasts (CAFs) critically regulate tumor progression, angiogenesis, metastasis, and therapeutic resistance. This study investigated the characteristics of CAFs in glioblastoma (GBM) and developed a CAF-based risk signature to predict patient prognosis. The single-cell RNA sequencing (scRNA-seq) data were sourced from the Gene Expression Omnibus (GEO) database, whereas the bulk RNA-seq datasets were retrieved from The Cancer Genome Atlas (TCGA) and Chinese Glioma Genome Atlas (CGGA), respectively.
View Article and Find Full Text PDFCell Commun Signal
August 2025
Department of Gastroenterology and Hepatology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Background: Cellular senescence plays a significant role in tumorigenesis and tumor progression. Substantial evidence indicates that senescence occurs in cancer-associated fibroblasts (CAFs), the predominant stromal component within the tumor microenvironment (TME), which profoundly impacts tumor biology. However, despite growing evidence of stromal cell involvement in cancer progression, the specific mechanisms and clinical implications of senescent CAFs (SCAFs) in hepatocellular carcinoma (HCC) have not been fully elucidated.
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