This book covers advanced and up-to-date analyses of the synthesis, fragmentation, and dysregulation of Small Leucine-Rich Proteoglycans (SLRPs) in some common matrix-related diseases. These SLRPs act as autonomous triggers of inflammation in conditions such as cancer, cartilage tissue degeneration, renal (kidney) diseases, as well as skin, tendon, musculoskeletal, and craniofacial tissues, responding to stress, injury, and impairment of normal function.

Chapters describe the significance behind the formation of proteolytic molecular fragments of SLRPs and why they alter inflammatory cell-signaling pathways, acting as Damage-Associated Molecular Patterns (DAMPs), that can function as Pathogen-Associated Molecular Patterns (PAMPs) in the early, intermediate, and advanced stages of matrix dysregulation and diseases. It also discusses evidence-based therapeutic approaches useful for identifying molecular fragments as potential biomarkers of matrix degeneration, providing a thorough understanding on the regulatory role of SLRPs in matrix homeostasis and diseases. The book is supplemented with well-illustrated figures, tabulated analysis, and critical review questions for further investigations that identifies gap in current understanding.

 The book is relevant for experts in medical sciences specializing in cell, extracellular matrix-based tissue analysis, researchers, as well as students interested in investigating matrix-related changes during the pathological progression of diseases.

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Includes class-wise description and comparisons of SLRPs in diseases of the matrix Provides easy-to-follow definitions with tabular analyses of SLRP fragments and critical review-based questions Discusses therapeutic approaches behind SLRPs fragments as potential biomarkers in diseases
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Produktdetaljer

ISBN
9789819678891
Publisert
2025-08-15
Utgiver
Springer Nature Switzerland AG
Høyde
235 mm
Bredde
155 mm
Aldersnivå
Professional/practitioner, P, UP, 06, 05
Språk
Product language
Engelsk
Format
Product format
Innbundet
Antall sider
24

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