Literature DB >> 12810158

Serum prolidase I activity and some bone metabolic markers in patients with breast cancer: in relation to menopausal status.

Zeynep Ozbek Kir1, Pernur Oner, Yildiz Oner Iyidoğan, Sembol Türkmen, Hikmet Koçak, Murat Koşer, Seden Ozbilen Küçücük.   

Abstract

OBJECTIVES: The purpose of this study was to investigate the diagnostic value of some osteoblastic/osteoclastic biochemical markers and serum prolidase I activity in breast cancer (BC). DESIGN AND METHODS: Serum bone gla protein (BGP), prolidase I activity, urinary deoxypyridinoline (Dpy) and calcium excretions were measured, in metastatic and nonmetastatic BC patients, and in 52 healthy women.
RESULTS: In patients with metastases, bone turnover markers were found to be significantly higher than those in the control group and in patients without metastases. Serum prolidase activity in patients with and without metastases was also significantly higher than those in the control group, but there was no difference between the two patient groups.
CONCLUSIONS: Bone turnover has been suggested to be accelerated in BC patients with the more pronounced osteolytic activation, especially in metastatic state. Serum prolidase in premenopausal period appears to be valuable in discriminating cancer patients from controls. BGP and to a lesser degree of Dpy, may be useful markers for predicting the metastatic bone involvement, as well as for the more cost effective management of BC patients and monitoring the effects of antiresorptive therapy of malignant osteolysis before any metastasis could be detected by other invasive techniques.

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Year:  2003        PMID: 12810158     DOI: 10.1016/s0009-9120(03)00028-6

Source DB:  PubMed          Journal:  Clin Biochem        ISSN: 0009-9120            Impact factor:   3.281


  3 in total

1.  Evaluation of the utility of serum prolidase as a marker for liver fibrosis.

Authors:  John C Stanfliet; Michael Locketz; Peter Berman; Tahir S Pillay
Journal:  J Clin Lab Anal       Date:  2014-05-05       Impact factor: 2.352

2.  Inhibition of ERBB2-overexpressing Tumors by Recombinant Human Prolidase and Its Enzymatically Inactive Mutant.

Authors:  Lu Yang; Yun Li; Arup Bhattacharya; Yuesheng Zhang
Journal:  EBioMedicine       Date:  2015-05-01       Impact factor: 8.143

3.  Identification of prolidase as a high affinity ligand of the ErbB2 receptor and its regulation of ErbB2 signaling and cell growth.

Authors:  L Yang; Y Li; Y Zhang
Journal:  Cell Death Dis       Date:  2014-05-08       Impact factor: 8.469

  3 in total

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