Background: CD44 is a cell-surface transmembrane glycoprotein that participates in the regulation of many cellular processes, including cell division, adhesion, migration and stem-like characteristics. CD63 is involved in the exocytosis process.
Objective: To evaluate the relationship between CD44 and CD63 expression and clinicopathological features, including tumor-infiltrating lymphocytes (TILs), phosphoinositide 3-kinase (PIK3CA) mutation and survival.
Methodology: CD44 and CD63 were stained in samples from 101 breast cancer cases from Peruvian women.
Results: Median age was 52 years, most were most were grade-3 (68%), estrogen receptor (ER)+ (64%) and stage II-III (92%). Median ki67 was 30%, median stromal TIL was 30% and mutation was found in 49%. Longer survival was associated with earlier stages ( = 0.016), lower ki67 ( = 0.023), ER+ ( = 0.034), luminal phenotype ( = 0.029) and recurrence ( < 0.001). CD44 was classified as high cell density staining in 57% and high intensity in 55%. High CD44 density was associated with younger age ( = 0.043), triple-negative phenotype ( = 0.035) and shorter survival ( = 0.005). High CD44 expression was associated with short survival ( = 0.005). High CD63 cell density was found in 56% of cases and was associated with ER-positive ( = 0.045), low TIL levels ( = 0.007), Luminal-A ( = 0.015) and low CD44 intensity ( = 0.032).
Conclusion: CD44 expression was associated with aggressive features and low CD63 density staining.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11489100 | PMC |
http://dx.doi.org/10.3332/ecancer.2024.1779 | DOI Listing |
Cytotechnology
February 2025
College of Veterinary Medicine, Qingdao Agricultural University, No. 700 Changcheng Road, Chengyang, Qingdao, 266109 China.
Osteoarthritis is a degenerative disease of cartilage, and exosome derived from mesenchymal stem cells (MSCs) are considered promising for treating inflammatory musculoskeletal disorders, although their mechanisms are not fully understood. This study aimed to investigate the effects of exosomes derived from canine bone marrow mesenchymal stem cells (cBMSCs-Exos) on the expression of inflammatory factors and genes related cartilage matrix metabolism in IL-1β-induced canine chondrocytes. Canine BMSCs were isolated and characterized for surface markers and trilineage differentiation.
View Article and Find Full Text PDFSci Rep
November 2024
Department of Oral Biology, Faculty of Dentistry, Mahidol University, 6 Yothi Road, Ratchathewi, Bangkok, 10400, Thailand.
Exosomes derived from the stem cells of human exfoliated deciduous teeth (SHED) hold promise for tissue regeneration. Apoptotic cells release a variety of extracellular vesicles that affect intercellular communication. This study aimed to investigate the angiogenic effects of SHED-derived exosomes modified via apoptosis induction on human umbilical vein endothelial cells (HUVECs).
View Article and Find Full Text PDFJ Nanobiotechnology
November 2024
Department of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China.
Objective: As research into preclinical rheumatoid arthritis (pre-RA) has advanced, a growing body of evidence suggests that abnormalities in RA-affected joint cartilage precede the onset of arthritis. Thus, early prevention and treatment strategies are imperative. In this study, we aimed to explore the protective effects of mesenchymal stem cell (MSC)-derived microvesicles (MVs) on cartilage degradation in a collagen-induced arthritis (CIA) mouse model.
View Article and Find Full Text PDFEcancermedicalscience
September 2024
Unidad de Ensayos Clinicos, Oncosalud-AUNA, Lima 15038, Peru.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!