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Background: Sarcoma is a rare and heterogeneous group of malignant tumors originating from mesenchymal tissues, which presents significant challenges for diagnosis and treatment. Ferroptosis, a newly recognized form of iron-dependent cell death, is distinct from other cell death mechanisms such as apoptosis and autophagy. Recent studies have shown that the induction of ferroptosis is an effective way to kill sarcoma cells and reduce their resistance to chemotherapeutic drugs, highlighting the importance of understanding how ferroptosis may influence the biology and treatment of sarcomas.
Methods: In this study, we employed three main methods, namely CiteSpace, VOSviewer, and the R package "bibliometrix", to analyze relevant literature. Publications related to ferroptosis and sarcoma in the Science Citation Index Expanded of the Web of Science Core Collection (WoSCC) database (2012-2023) were included, and bioinformatics analyses were performed using R Studio and public databases.
Results: The analysis revealed that research on sarcomas and ferroptosis has experienced a steady increase over the years, with a diverse range of research topics and collaborations established among researchers worldwide. The key findings include the identification of influential authors and institutions, prominent research clusters, and emerging research trends. The bioinformatics analysis results confirmed the significance of ferroptosis-related gene ACSF2 in different sarcomas. Notably, the scarcity of studies focusing on the relationship between sarcoma and ferroptosis has been observed, highlighting the potential for further exploration in this area.
Conclusion: The integration of bibliometrics and bioinformatics provides valuable insights into the research landscape of sarcoma and ferroptosis. Future research on ferroptosis will continue to focus on its mechanisms in sarcomas including immune microenvironment, while also further exploring its potential clinical applications. We have identified a potential ferroptosis-related gene, ACSF2, which shows associations with survival in sarcoma datasets. Further testing is needed to validate its potential as a prognostic biomarker.
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http://dx.doi.org/10.1007/s12672-025-03389-z | DOI Listing |
Chembiochem
September 2025
School of Pharmaceutical Science and Technology, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, Hangzhou, 310024, P. R. China.
The ATPase caseinolytic protease X (ClpX), forming the ClpXP complex with caseinolytic protease P (ClpP), is essential for mitochondrial protein homeostasis. While ClpP targeting is a recognized anticancer strategy, the role of ClpX in cancer remains underexplored. In pancreatic ductal adenocarcinoma (PDAC), elevated CLPX expression correlates with poor prognosis, suggesting its oncogenic function.
View Article and Find Full Text PDFKidney Blood Press Res
September 2025
Objective: Cisplatin-induced acute kidney injury (Cis-AKI) is a significant cause of renal damage, characterized by tubular injury, ferroptosis, and oxidative stress. While therapeutic options for Cis-AKI remain limited, identifying novel targets to prevent kidney injury is critical. This study focuses on GALNT14, a gene associated with ferroptosis, and its potential role in mitigating Cis-AKI.
View Article and Find Full Text PDFStem Cell Rev Rep
September 2025
Paris Cité University, INSERM UMR-S 970, Paris Cardiovascular Research Centre, Paris, France.
Endothelial Colony-Forming Cells (ECFCs) are recognized as key vasculogenic progenitors in humans and serve as valuable liquid biopsies for diagnosing and studying vascular disorders. In a groundbreaking study, Anceschi et al. present a novel, integrative strategy that combines ECFCs loaded with gold nanorods (AuNRs) to enhance tumor radiosensitization through localized hyperthermia.
View Article and Find Full Text PDFCell Death Differ
September 2025
Department of Neurology, China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Oncogene
September 2025
Department of Breast Surgery, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Cholesterol biosynthesis is more activated in triple negative breast cancer (TNBC) than in other subtype breast cancer and plays essential role in facilitating TNBC. However, the regulatory network and how cholesterol biosynthesis contribute to TNBC development and progression are not well elucidated. Here, we found that reticulum membrane protein complex 2 (EMC2) is highly expressed in TNBC and predicts short survival of patients.
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