Analysis of glycosaminoglycans in human prostate by high-performance liquid chromatography

被引:22
作者
Iida, S
Suzuki, K
Matsuoka, K
Takazono, I
Shimada, A
Inoue, M
Yahara, J
Noda, S
机构
[1] KURUME UNIV, SCH MED, DEPT CHEM, KURUME, FUKUOKA 830, JAPAN
[2] KANAZAWA MED UNIV, DEPT UROL, KANAZAWA, ISHIKAWA, JAPAN
来源
BRITISH JOURNAL OF UROLOGY | 1997年 / 79卷 / 05期
关键词
proteoglycan; glycosaminoglycans (GAGs); human prostate; high-performance liquid chromatography (HPLC);
D O I
10.1046/j.1464-410X.1997.00135.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objective To investigate changes in glycosaminoglycan (GAG) profiles in human prostatic tissue. Materials and methods Seventeen human prostatic samples were examined; five were normal, six hyperplastic and six were cancerous. Prostatic proteoglycans were extracted with 4 mol/L guanidine-HCl containing protease inhibitors. After digestion of the freeze-dried proteoglycan extract with papain, the prostatic GAGs were purified. Total GAGs were measured by a modified dimethylmethylene blue (DMB) method. Highperformance liquid chromatography (HPLC) was used to quantify the extracted GAGs. Results Six types of GAGs, i.e, chondroitin 4-sulphate (Ch-4S), chondroitin 6-sulphate (Ch-6S), dermatan sulphate (DS), chondroitin, heparan sulphate and hyaluronic acid, were analysed qualitatively and quantitatively. The total amount of GAGs was increased in hyperplastic and cancerous prostates, with the predominant components being DS and Ch-6S in these specimens. The Ch-S:DS ratio in cancerous prostate was significantly higher than that in normal and BPH tissue (P < 0.05). Moreover, chondroitin was increased in hyperplastic prostatic tissue (P < 0.01). Conclusions These results suggest that an increase in chondroitin levels may be associated with hyperplastic change and an increase in the Ch-S:DS ratio may be related to the development of malignancy.
引用
收藏
页码:763 / 769
页数:7
相关论文
共 32 条
[21]   DEVELOPMENTAL-CHANGES IN THE SYNTHESIS OF GLYCOSAMINOGLYCANS AND COLLAGEN IN EMBRYONIC CHICK SKIN [J].
NAKAMURA, T ;
NAGAI, Y .
JOURNAL OF BIOCHEMISTRY, 1980, 87 (02) :629-637
[22]   STABILITY OF BOVINE NASAL CARTILAGE PROTEOGLYCANS DURING ISOLATION AND STORAGE [J].
PEARSON, JP ;
MASON, RM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 498 (01) :176-188
[23]   PROTEOGLYCANS AS MODULATORS OF GROWTH-FACTOR ACTIVITIES [J].
RUOSLAHTI, E ;
YAMAGUCHI, Y .
CELL, 1991, 64 (05) :867-869
[24]   RELEASE OF BASIC FIBROBLAST GROWTH FACTOR-HEPARAN SULFATE COMPLEXES FROM ENDOTHELIAL-CELLS BY PLASMINOGEN ACTIVATOR-MEDIATED PROTEOLYTIC ACTIVITY [J].
SAKSELA, O ;
RIFKIN, DB .
JOURNAL OF CELL BIOLOGY, 1990, 110 (03) :767-775
[25]   CHANGES IN SULFATED MUCOPOLYSACCHARIDE COMPOSITION OF MAMMALIAN-TISSUES DURING GROWTH AND IN CANCER TISSUES [J].
SAMPAIO, LO ;
DIETRICH, CP ;
FILHO, OG .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 498 (01) :123-131
[26]  
SCHAMHART DHJ, 1994, WORLD J UROL, V12, P55
[27]   DERMATAN SULFATE-RICH PROTEOGLYCAN ASSOCIATES WITH RAT TAIL TENDON COLLAGEN AT THE D-BAND IN THE GAP REGION [J].
SCOTT, JE ;
ORFORD, CR .
BIOCHEMICAL JOURNAL, 1981, 197 (01) :213-&
[28]  
TAKEUCHI J, 1976, CANCER RES, V36, P2133
[29]  
VONIOZZO R, 1981, CANCER-AM CANCER SOC, V48, P89, DOI 10.1002/1097-0142(19810701)48:1<89::AID-CNCR2820480118>3.0.CO
[30]  
2-B