Serum midkine levels are increased in patients with various types of carcinomas

被引:154
作者
Ikematsu, S
Yano, A
Aridome, K
Kikuchi, M
Kumai, H
Nagano, H
Okamoto, K
Oda, M
Sakuma, S
Aikou, T
Muramatsu, H
Kadomatsu, K
Muramatsu, T
机构
[1] Nagoya Univ, Sch Med, Dept Biochem, Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Meiji Cell Technol Ctr, Odawara, Kanagawa 2500862, Japan
[3] Kagoshima Univ, Fac Med, Dept Surg, Kagoshima 890, Japan
[4] Univ Occupat & Environm Hlth, Dept Med Technol, Yahatanishi Ku, Kitakyushu, Fukuoka, Japan
[5] Univ Occupat & Environm Hlth, Dept Surg, Yahatanishi Ku, Kitakyushu, Fukuoka, Japan
[6] Nagoya Univ, Sch Med, Dept Biochem, Showa Ku, Nagoya, Aichi 4668550, Japan
关键词
enzyme-linked immunoassay; growth factor; midkine; serum; tumour marker;
D O I
10.1054/bjoc.2000.1339
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The level of expression of midkine (MK), a heparin-binding growth factor, is increased in many types of human carcinomas. An enzyme-linked immunoassay, which utilizes a combination of rabbit and chicken antibodies revealed that serum MK level in the controls (n = 135) was 0.154 +/- 0.076 (mean +/- SD) ng ml(-1) with an apparent cut-off value as 0.5 ng ml(-1). Serum MK level was significantly elevated in the cancer patients (n = 150) (P < 0.001); 87% of the patients showed levels of more than 0.5 ng ml(-1). All ten types of cancer examined showed a similar profile of serum MK level. There was no or weak correlation between C-reactive protein level, a marker of inflammation, and serum MK level. Furthermore, in case of gastric carcinoma and lung carcinoma, patients with stage I carcinoma already showed elevated serum MK levels. The present results indicated that serum MK could serve as a general tumour marker with a good potential for clinical application. (C) 2000 Cancer Research Campaign.
引用
收藏
页码:701 / 706
页数:6
相关论文
共 27 条
[1]   INCREASED MIDKINE GENE-EXPRESSION IN HUMAN GASTROINTESTINAL CANCERS [J].
ARIDOME, K ;
TSUTSUI, J ;
TAKAO, S ;
KADOMATSU, K ;
OZAWA, M ;
AIKOU, T ;
MURAMATSU, T .
JAPANESE JOURNAL OF CANCER RESEARCH, 1995, 86 (07) :655-661
[2]  
Choudhuri R, 1997, CANCER RES, V57, P1814
[3]  
GARVER RI, 1994, CANCER, V74, P1584, DOI 10.1002/1097-0142(19940901)74:5<1584::AID-CNCR2820740514>3.0.CO
[4]  
2-V
[5]   Neointima formation in a restenosis model is suppressed in midkine-deficient mice [J].
Horiba, M ;
Kadomatsu, K ;
Nakamura, E ;
Muramatsu, H ;
Ikematsu, S ;
Sakuma, S ;
Hayashi, K ;
Yuzawa, Y ;
Matsuo, S ;
Kuzuya, M ;
Kaname, T ;
Hirai, M ;
Saito, H ;
Muramatsu, T .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (04) :489-495
[6]  
ISHIKAWA E, 1993, ANN NY ACAD SCI, V420, P74
[7]   CDNA CLONING AND SEQUENCING OF A NEW GENE INTENSELY EXPRESSED IN EARLY DIFFERENTIATION STAGES OF EMBRYONAL CARCINOMA-CELLS AND IN MID-GESTATION PERIOD OF MOUSE EMBRYOGENESIS [J].
KADOMATSU, K ;
TOMOMURA, M ;
MURAMATSU, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 151 (03) :1312-1318
[8]   Midkine induces the transformation of NIH3T3 cells [J].
Kadomatsu, K ;
Hagihara, M ;
Akhter, S ;
Fan, QW ;
Muramatsu, H ;
Muramatsu, T .
BRITISH JOURNAL OF CANCER, 1997, 75 (03) :354-359
[9]   MIDKINE ENHANCES FIBRINOLYTIC-ACTIVITY OF BOVINE ENDOTHELIAL-CELLS [J].
KOJIMA, S ;
MURAMATSU, H ;
AMANUMA, H ;
MURAMATSU, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (16) :9590-9596
[10]   Immunohistochemical analysis of Midkine expression in human prostate carcinoma [J].
Konishi, N ;
Nakamura, M ;
Nakaoka, S ;
Hiasa, Y ;
Cho, M ;
Uemura, H ;
Hirao, Y ;
Muramatsu, T ;
Kadomatsu, K .
ONCOLOGY, 1999, 57 (03) :253-257