The decrease in prolidase activity in myeloproliferative neoplasms

• Published in: Advances in clinical and experimental medicine : official organ Wroclaw Medical University Vol. 21; no. 6; pp. 767 - 771
• Main Authors: Nowicka, Jadwiga, Nahaczewska, Wiesława, Owczarek, Henryk, Woźniak, Mieczysław
• Format: Journal Article
• Language: English
• Published: Poland 01.11.2012
• Subjects: Adult; Aged; Biomarkers, Tumor - metabolism; Bone Marrow Neoplasms - enzymology; Bone Marrow Neoplasms - physiopathology; Bone Remodeling; Case-Control Studies; Connective Tissue - pathology; Connective Tissue - physiopathology; Dipeptidases - metabolism; Female; Humans; Male; Middle Aged; Young Adult
• ISSN: 1899-5276

The development of bone marrow fibrosis is a severe complication in hematological diseases. The progress of bone marrow myelofibrosis is evaluated by a trephine examination and may be characterized by the biochemical markers of collagen turnover determination. Investigation of serum prolidase activity and biochemical markers of collagen metabolism in order to establish its role in the development of bone marrow fibrosis. The group of 37 patients with myeloproliferative neoplasms (MPN) before treatment, consisted of 16 patients with chronic myeloid leukemia (CML), 7 with primary myelofibrosis (PMF), 8 with essential thrombocythopenia (ET), and 6 with polycythemia vera (PV). It was found that the plasma activity of prolidase (Pro) was reduced to almost half together with the serum level of osteocalcin (BGL), and hydroxyproline (H-PRO) in the serum and urine of patients with MPN in comparison to the control group. In the MPN group of patients, the levels of N-terminal procollagen III peptide (PIIINP), type I procollagen (PICP) and the C-terminal telopeptide of type I collagen (ICTP) were significantly higher. The alteration of collagen turnover markers in the MPN patient group (the elevation of synthesis and inhibition of collagen catabolism rate) has suggested that a diminished prolidase activity may contribute to such alteration of collagen metabolism and should be consider a biomarker of MPN progress.