Title of article :
Serum prolidase I activity and some bone metabolic markers in patients with breast cancer: in relation to menopausal status
Author/Authors :
Zeynep ?zbek K?r، نويسنده , , Pernur ?ner، نويسنده , , Y?ld?z ?ner Iyido an، نويسنده , , Sembol Türkmen، نويسنده , , Hikmet Koçak، نويسنده , , Murat Ko er، نويسنده , , Seden ?zbilen Küçücük، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2003
Pages :
6
From page :
289
To page :
294
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.
Keywords :
breast cancer , menopausal status , Bone metastases , bone turnover markers , Bone involvement , Serum prolidase I
Journal title :
Clinical Biochemistry
Serial Year :
2003
Journal title :
Clinical Biochemistry
Record number :
482410
Link To Document :
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