URINARY LAMININ FRAGMENTS AS A TUMOR-MARKER POTENTIALLY REFLECTING BASEMENT-MEMBRANE DESTRUCTION

被引:22
作者
KATAYAMA, M
KAMIHAGI, K
HIRAI, S
KUROME, T
MURAKAMI, K
HINO, F
KATO, I
机构
[1] Biotechnology Research Laboratory, Takara Shuzo Co. Ltd, Otsu, 520-21
关键词
D O I
10.1038/bjc.1992.105
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The presence of soluble laminin fragments in urine of healthy subjects, patients with diabetes, and patients with tumours was studied using sandwich immunoenzymometric assay technique. The form of urinary laminin (ULN) fragments was dramatically different from that of intact laminin, so ULN could be detected only by using monoclonal antibodies. Mean levels of ULN in lung tumour were significantly higher (171-mu-g gram-1 creatinine) than those in healthy subjects, patients with diabetes, patients with stomach tumour, and patients with colon tumour (respectively 91, 92, 77 and 53-mu-g gram-1 creatinine). Immunopurified ULN fragments showed an apparent molecular mass of 42 KD on electrophoresis. This fragment was recognised as being derived from the N-terminal region of laminin B2 chain, because the N-terminal residues of ULN were found to be completely homologous to B2 chain. These data suggested that ULN was almost all fragmented, consisted mainly of N-terminal domain of the B2 chain, and was suspected of a tumour-associated protein fragments probably derived from basement membrane degraded proteolytically by tumour cells. ULN, increased in tumour patients, could be a potential clinical marker for monitoring the turnover of basement membrane in tumours.
引用
收藏
页码:509 / 514
页数:6
相关论文
共 28 条
[1]   THE INVITRO INVASIVENESS AND INTERACTIONS WITH LAMININ OF K-1735 MELANOMA-CELLS - EVIDENCE FOR DIFFERENT LAMININ-BINDING AFFINITIES IN HIGH AND LOW METASTATIC VARIANTS [J].
ALBINI, A ;
AUKERMAN, SL ;
OGLE, RC ;
NOONAN, DM ;
FRIDMAN, R ;
MARTIN, GR ;
FIDLER, IJ .
CLINICAL & EXPERIMENTAL METASTASIS, 1989, 7 (04) :437-451
[2]  
ALBRECHTSEN R, 1981, CANCER RES, V41, P5076
[3]   STRUCTURE AND FUNCTION OF LAMININ - ANATOMY OF A MULTIDOMAIN GLYCOPROTEIN [J].
BECK, K ;
HUNTER, I ;
ENGEL, J .
FASEB JOURNAL, 1990, 4 (02) :148-160
[4]  
BONSNES RW, 1945, J BIOL CHEM, V158, P581
[5]  
BOYD D, 1989, CANCER RES, V49, P816
[6]  
BROCKS DG, 1986, CLIN CHEM, V32, P787
[7]  
Harlow E, 1988, ANTIBODIES LAB MANUA, P139
[8]   FIBRONECTINS - MULTIFUNCTIONAL MODULAR GLYCOPROTEINS [J].
HYNES, RO ;
YAMADA, KM .
JOURNAL OF CELL BIOLOGY, 1982, 95 (02) :369-377
[9]  
Jones P A, 1982, Cancer Metastasis Rev, V1, P289, DOI 10.1007/BF00124214
[10]   EFFECTS OF EXPERIMENTAL NEPHROSIS ON BASEMENT-MEMBRANE COMPONENTS AND ENZYMES OF COLLAGEN BIOSYNTHESIS IN RAT-KIDNEY [J].
JUKKOLA, A ;
RISTELI, J ;
AUTIOHARMAINEN, H ;
RISTELI, L .
BIOCHEMICAL JOURNAL, 1985, 226 (01) :243-250