Serum levels of bone sialoprotein, osteopontin, and β2-microglobulin in stage I of multiple myeloma.
Bone sialoprotein
multiple myeloma stage I
osteopontin
β2-microglobulin
Journal
Journal of cancer research and therapeutics
ISSN: 1998-4138
Titre abrégé: J Cancer Res Ther
Pays: India
ID NLM: 101249598
Informations de publication
Date de publication:
Historique:
entrez:
5
5
2020
pubmed:
5
5
2020
medline:
2
10
2020
Statut:
ppublish
Résumé
The fluctuations of proteins in multiple myeloma (MM) are well-known markers for checking the status of the patients. The objective of this study was to examine three proteins that have an important role in disease progression. The study was performed with two groups: 30 MM stage I patients' (14 females/16 males; aged 60.83 ± 12.38 years) as case group and 40 healthy individuals (18 females/22 males; aged 57.65 ± 6.43 years) as control group. Both groups have been matched in gender and age. Bone sialoprotein (BSP), osteopontin (OPN), and β2-microglobulin (β2M) were measured with an enzyme-linked immunosorbent assay. Serum BSP levels of MM-I patients was significantly higher than that of healthy controls (29.24 ± 5.57 vs. 20.89 ± 3.67, P = 0.001). OPN levels of MM-I patients were significantly lower than that of healthy individuals (12.03 ± 3.45 vs. 19.35 ± 4.67, P = 0.001). β2M levels of patients and controls were similar (1.49 ± 0.67 vs. 1.29 ± 0.55, P = 0.193). The results suggested that myeloma cells may affect the production of BSP and OPN, which possibly contributes to osteoclastic bone resorption in MM-I patients. Their levels may be a useful biomarker for assessing bone destruction in MM-I patients and distinguishing MM-I from healthy individuals.
Identifiants
pubmed: 32362616
pii: JCanResTher_2020_16_1_98_263540
doi: 10.4103/jcrt.JCRT_666_16
doi:
Substances chimiques
Biomarkers, Tumor
0
Integrin-Binding Sialoprotein
0
SPP1 protein, human
0
beta 2-Microglobulin
0
Osteopontin
106441-73-0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
98-101Déclaration de conflit d'intérêts
None