Effects of Zoledronic Acid on Proteinase Plasma Levels in Patients with Bone Metastases

Background: The effects of the bisphosphonate derivative zoledronic acid (ZA) on the circulating levels of matrix metalloproteinase-2 (MMP-2), matrix metallo-proteinases-9 (MMP-9), cathepsin B (Cath B) and urokinase-type plasminogen activator (uPA) in patients with bone metastasis (BMTS) and the pos...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Anticancer research 2006-01, Vol.26 (1A), p.23-26
Hauptverfasser: LETO, Gaetano, BADALAMENTI, Giuseppe, ARCARA, Carlo, CRESCIMANNO, Marilena, FLANDINA, Carla, TUMMINELLO, Francesca Maria, INCORVAIA, Lorena, GEBBIA, Nicola, FULFARO, Fabio
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Background: The effects of the bisphosphonate derivative zoledronic acid (ZA) on the circulating levels of matrix metalloproteinase-2 (MMP-2), matrix metallo-proteinases-9 (MMP-9), cathepsin B (Cath B) and urokinase-type plasminogen activator (uPA) in patients with bone metastasis (BMTS) and the possible correlation with the symptomatic response induced by this drug in these patients were evaluated. Patients and Methods: Proteinase levels were determined by enzyme-linked immunosorbent assay (ELISA) in the plasma of 30 patients with painful bone metastases from breast or prostate cancer undergoing multiple treatment with ZA (4 mg i.v., every 4 weeks). Healthy subjects (HS) of both genders (12 female and 30 male) served as the control group. The symptomatic response to ZA was assessed by the visual analog scale score (VAS). Results: The median MMP-2 and MMP-9 pretreatment levels were more elevated in BMTS as compared to HS (p≤0.0001). Conversely, uPA levels were lower in BMTS p=0.0033; no significant difference was observed for Cath B. ZA administration was associated with a symptomatic response (VAS score≤4) in 25/30 patients (83.3%) (p
ISSN:0250-7005
1791-7530