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In recent years, some circRNAs and RNA methylation enzymes (including RNA methyltransferases and RNA demethylases) have been reported to be associated to the prognosis of bladder cancer, but the findings have been inconsistent. Therefore, the aims of this study is to comprehensively evaluate the prognostic value of circRNAs and RNA methylation enzymes as a whole in bladder cancer by Meta-analysis. A comprehensive literature search was performed in PubMed, Cochrane Library, EMbase, Web of Science, CNKI, WanFang, and VIP databases from the establishment of the database to March 2024. Data were extracted from the included literature and statistically analyzed using Stata 18.0 MP. (1) Overall survival (OS): high expression of circRNAs decreased OS of bladder cancer (HR = 1.74, 95% CI: 1.26-2.41, P = 0.001); and high fat mass and obesity-associated protein (FTO) expression led to poor OS in bladder cancer (HR = 2.38, 95% CI: 1.08-2.25, P = 0.032). (2) Disease-free survival (DFS): low circRNAs expression resulted in poor DFS (HR = 1.74, 95% CI: 1.38-2.18, P < 0.001); (3) Recurrence-free survival (RFS): high expression of circ-CCT3 and circ-RHOT1 decreased bladder cancer patients' RFS (HR = 2.26, 95% CI: 1.63-3.12, P < 0.001); and low expression of circ0004826 and circ0077837 also affected RFS (HR = 0.19, 95% CI: 0.08-0.43, P < 0.001). (4) 5-year survival: high expression of circRNAs decreased 5-year survival of bladder cancer patients (HR = 3.26, 95% CI: 1.90-5.57, P < 0.001). CircRNAs and FTO can be prognostic factors for bladder cancer.
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http://dx.doi.org/10.1016/j.urolonc.2025.06.005 | DOI Listing |
Mol Carcinog
September 2025
Department of Urology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
B cells located in tertiary lymphoid structures (TLSs) may undergo clonal expansion, somatic hypermutation, isotype switching, and tumor-specific antibody production, suggesting that antibody-producing plasma cells may be involved in antitumor immunity. This study used a combination of single-cell sequencing (five samples from our center, and four samples from PRJNA662018) and spatial transcriptome (one sample from our center, and four samples from GSE169379) research methods to investigate the relationship between TLSs and the immunoglobulin repertoire in muscle invasive bladder cancer (MIBC). 405 patients with MIBC from TCGA and 348 patients with metastatic urothelial carcinoma on PD-L1 inhibitor treatment from the IMvigor210 trial were included in this study.
View Article and Find Full Text PDFUrol Case Rep
September 2025
Main Line Health, Division of Urology, Wynnewood, PA, USA.
Muscle-invasive bladder cancer (MIBC) with cardiac metastasis typically carries a very poor prognosis. A Black woman in her 70s developed high-grade urothelial carcinoma with squamous differentiation invading the bladder muscle. Despite chemotherapy, radiation, and nephrostomy, the disease progressed.
View Article and Find Full Text PDFFront Oncol
August 2025
Department of Medical Oncology, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua Medicine, Tsinghua University, Beijing, China.
In metastatic colorectal cancer (mCRC) patients with proficient mismatch repair (pMMR)/microsatellite stability (MSS), beyond third-line therapies were extremely limited. Here, we reported a case of a 21-year-old male patient with pMMR/MSS mCRC who failed to respond to both first- and second-line treatment and subsequently received non-standard third-line therapy at a local hospital. This patient was referred to our hospital, and we initiated salvage therapies.
View Article and Find Full Text PDFFront Oncol
August 2025
Department of Physiology, School of Basic Medical Sciences, Nanjing Medical University, Nanjing, Jiangsu, China.
Purpose: Bladder cancer (BLCA) is one of the most common urogenital malignancies in the world. The stroma of the tumor microenvironment (TME) largely affects the progression of BLCA. However, a stroma-relevant biomarker for predicting BLCA progression is still lacking.
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