Cytokine, Год журнала: 2024, Номер 180, С. 156673 - 156673
Опубликована: Июнь 9, 2024
Язык: Английский
Cytokine, Год журнала: 2024, Номер 180, С. 156673 - 156673
Опубликована: Июнь 9, 2024
Язык: Английский
Proteoglycan Research, Год журнала: 2024, Номер 2(4)
Опубликована: Окт. 1, 2024
Proteoglycans and their proteolytic fragments diffuse into biological fluids such as plasma, serum, urine, or synovial fluid, where they can be detected by antibodies mass-spectrometry. Neopeptides generated the proteolysis of proteoglycans are recognized specific neoepitope act a proxy for activity certain proteases. Proteoglycan proteoglycan potentially used prognostic, diagnostic, theragnostic biomarkers several diseases characterized dysregulated extracellular matrix remodeling osteoarthritis, rheumatoid arthritis, atherosclerosis, thoracic aortic aneurysms, central nervous system disorders, viral infections, cancer. Here, we review main mechanisms accounting presence soluble in fluids, potential application biomarkers, highlight challenges opportunities ahead clinical translation.
Язык: Английский
Процитировано
3International Journal of Molecular Sciences, Год журнала: 2025, Номер 26(10), С. 4743 - 4743
Опубликована: Май 15, 2025
Despite several years passing since the COVID-19 pandemic was declared, challenges remain in understanding factors that can predict severity of disease and complications SARS-CoV-2 infection. While many large-scale multi-omic datasets have been published, integration these has potential to substantially increase biological insight gained, allowing a more complex comprehension pathogenesis. Such may improve our ability progression, detect severe cases rapidly develop effective therapeutics. In this study, we applied an innovative machine learning algorithm delineate COVID based on paired samples proteomic transcriptomic data from small cohort patients testing positive for infection with differential severity. Targeted plasma proteomics onco-immune targeted panel were performed sequential 23 severe, 21 moderate 10 mild patients. We DIABLO, new integrative method, identify multi-omics biomarker panels discriminate between multiple phenotypic groups, such as varied As is known among sample group, train models using outcome variable calculate features are important predictors disease. highly correlated key variables discriminant analysis methods. This approach highlights power patients, offering better molecular mechanisms driving opportunity prediction trajectories
Язык: Английский
Процитировано
0Cytokine, Год журнала: 2024, Номер 180, С. 156673 - 156673
Опубликована: Июнь 9, 2024
Язык: Английский
Процитировано
1