EXPRESSION OF METALLOPROTEINASE GENES IN HUMAN PROSTATE-CANCER

被引:201
作者
PAJOUH, MS
NAGLE, RB
BREATHNACH, R
FINCH, JS
BRAWER, MK
BOWDEN, GT
机构
[1] UNIV ARIZONA, SCH MED, DEPT PATHOL, TUCSON, AZ 85721 USA
[2] UNIV ARIZONA, SCH MED, DEPT RADIAT ONCOL, TUCSON, AZ 85721 USA
[3] UNIV NANTES, UFR MED, INSERM, U211, F-44035 NANTES, FRANCE
[4] UNIV WASHINGTON, DEPT SURG, DIV UROL, SEATTLE, WA 98195 USA
关键词
METALLOPROTEINASE; COLLAGENASE; PROSTATE ADENOCARCINOMA; MATRIX METALLOPROTEINASE-7 (MMP-7);
D O I
10.1007/BF01613138
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Twenty-five surgical specimens of malignant human prostate, 3 lymph nodes with metastatic prostate carcinoma, 11 normal human prostates, as well as 3 human prostate cell lines (DU-145, PC3 and LNCaP) were examined for the expression of the human matrix metalloproteinase-7 gene (MMP-7) from the human collagenase family (originally called PUMP-1 for putative metalloproteinase-1)[Quantin et al. (1989) Biochemistry 28:5327-5334; Muller et al. (1988) Biochem J 253:187-192; Matrisian and Bowden (1990) Semin Cancer Biol 1:107-115]. Northern blots were prepared using total RNA extracted from 18 prostate adenocarcinomas, 2 lymph nodes with metastatic prostate carcinoma and 11 normal human prostates. When the northern blots were hybridized with a P-32-labeled MMP-7 cDNA probe, a 1.2-kb mRNA was detected in 14 out of 18 prostate adenocarcinomas, 1 out of 2 metastatic lymph nodes, and 3 out of 11 normal prostates. The 3 human prostate cell lines did not show any evidence of the MMP-7 transcript. In situ hybridization was conducted to localize the MMP-7 mRNA to individual cells using a S-35-labeled MMP-7 cRNA. In situ hybridization was carried out on snap-frozen tissue sections of 7 prostate adenocarcinomas and 3 lymph nodes containing metastatic prostate adenocarcinoma using the same tissues previously probed by northern analysis as well as new samples. In situ hybridization revealed that the MMP-7 gene was expressed in the epithelial cells of primary prostate adenocarcinoma as well as in invasive and metastatic cells. MMP-7 expression was also seen focally in some dysplastic glands but not in stroma. Additional northern blot analysis was performed using probes to human type-IV collagenase, type-I collagenase and stromelysin I in human prostate adenocarcinoma as well as normal prostate tissue. Our results indicated that 6 out of 10 adenocarcinoma samples and none of the 4 normal samples were positive for type-IV collagenase transcripts. Tissue samples were also examined for the expression of type-I collagenase (9 adenocarcinomas and 4 normal) and stromelysin I (13 adenocarcinomas) by northern analysis. None of the tissues was found to express the transcripts of interest at detectable levels. These data suggest that certain metalloproteinases are present in prostatic adenocarcinoma and may play a role in invasion and metastasis.
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页码:144 / 150
页数:7
相关论文
共 22 条
[1]  
ABRAMSON M, 1975, ANN OTO RHINOL LARYN, V84, P158, DOI 10.1177/000348947508400203
[2]   QUANTITATION AND IMMUNOCYTOCHEMICAL LOCALIZATION OF HUMAN-SKIN COLLAGENASE IN BASAL-CELL CARCINOMA [J].
BAUER, EA ;
GORDON, JM ;
REDDICK, ME ;
EISEN, AZ .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1977, 69 (04) :363-367
[3]   THE ETIOPATHOGENESIS OF PROSTATIC-CANCER WITH SPECIAL REFERENCE TO ENVIRONMENTAL-FACTORS [J].
BOSLAND, MC .
ADVANCES IN CANCER RESEARCH, 1988, 51 :1-106
[4]  
DOBLE A, 1987, PRACTITIONER, V231, P239
[5]   LATENT CARCINOMA OF THE PROSTATE [J].
FRANKS, LM .
JOURNAL OF PATHOLOGY AND BACTERIOLOGY, 1954, 68 (02) :603-&
[6]  
FUCHS ME, 1989, MODERN PATHOL, V2, P105
[7]   LATENT PROSTATIC-CANCER IN A CONSECUTIVE AUTOPSY SERIES [J].
HOLUND, B .
SCANDINAVIAN JOURNAL OF UROLOGY AND NEPHROLOGY, 1980, 14 (01) :29-35
[8]  
HOROSZEWICZ JS, 1983, CANCER RES, V43, P1809
[9]  
KAIGHN ME, 1979, INVEST UROL, V17, P16
[10]   THE SIMULTANEOUS EXTRACTION OF HIGH-MOLECULAR-WEIGHT DNA AND OF RNA FROM SOLID TUMORS [J].
KRIEG, P ;
AMTMANN, E ;
SAUER, G .
ANALYTICAL BIOCHEMISTRY, 1983, 134 (02) :288-294