Increased concentration of soluble E-selectin in the sera of breast cancer patients

被引:0
作者
Matsuura, N
Narita, T
Mitsuoka, C
Kimura, N
Kannagi, R
Imai, T
Funahashi, H
Takagi, H
机构
[1] AICHI CANC CTR,RES INST,LAB EXPT PATHOL,CHIKUSA KU,NAGOYA,AICHI 464,JAPAN
[2] NAGOYA UNIV,SCH MED,DEPT SURG 2,SHOWA KU,NAGOYA,AICHI 466,JAPAN
关键词
breast cancer; cell adhesion molecules; E-selectin;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
E-selectin which is expressed on endothelial cells plays an important role in the adhesion of cancer cells to the vascular endothelium, being the ligand for a carbohydrate antigen expressed on cancer cells. In this study, the clinical usefulness of this protein was examined. E-selectin was expressed on the endothelial cells of the small vessels adjacent to the cancer nests in 63 of the 104 ( 60.6 %) primary tumors of breast cancer. The expression of E-selectin in locations adjacent to the cancer nests was more pronounced than that in distant ones. The mean value of serum soluble E-selectin (ng / mi) was 38.3 in benign breast disease, 47.8 in those with no evidence of recurrence, 49.4 in stage I / II primary breast cancer, 75.8 in stage III / IV primary breast cancer; and 93.7 in recurrent breast cancer. The mean value of serum soluble E-selectin was 106.2 ng / mi in patients with distant metastases, and 50.4 ng / mi in those with no evidence of distant metastases. Thus, the concentration of soluble E-selectin was significantly elevated in the sera of patients with distant metastases. These findings suggested that cancer cells induced the expression of E-selectin on endothelial cells and, that serum soluble E-selectin is useful as a tumor marker having a close relationship to metastasis in breast cancer.
引用
收藏
页码:1367 / 1372
页数:6
相关论文
共 22 条
[1]   CIRCULATING INTERCELLULAR-ADHESION MOLECULE-1 (ICAM-1), E-SELECTIN AND VASCULAR CELL-ADHESION MOLECULE-1 (VCAM-1) IN HUMAN MALIGNANCIES [J].
BANKS, RE ;
GEARING, AJH ;
HEMINGWAY, IK ;
NORFOLK, DR ;
PERREN, TJ ;
SELBY, PJ .
BRITISH JOURNAL OF CANCER, 1993, 68 (01) :122-124
[2]   IDENTIFICATION OF AN INDUCIBLE ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE [J].
BEVILACQUA, MP ;
POBER, JS ;
MENDRICK, DL ;
COTRAN, RS ;
GIMBRONE, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (24) :9238-9242
[3]   SELECTINS [J].
BEVILACQUA, MP ;
NELSON, RM .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (02) :379-387
[4]   Redirection of tumor metastasis by expression of E-selectin in vivo [J].
Biancone, L ;
Araki, M ;
Araki, K ;
Vassalli, P ;
Stamenkovic, I .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (02) :581-587
[5]  
Ferdeghini M, 1995, ANTICANCER RES, V15, P2255
[6]   THE INCREASED EXPRESSION OF ADHESION MOLECULES ICAM-3, E-SELECTIN AND P-SELECTIN ON BREAST-CANCER ENDOTHELIUM [J].
FOX, SB ;
TURNER, GDH ;
GATTER, KC ;
HARRIS, AL .
JOURNAL OF PATHOLOGY, 1995, 177 (04) :369-376
[7]   NOVEL ENDOTHELIAL-CELL ACTIVATION FACTOR(S) RELEASED FROM ACTIVATED PLATELETS WHICH INDUCE E-SELECTIN EXPRESSION AND TUMOR-CELL ADHESION TO ENDOTHELIAL-CELLS - A PRELIMINARY NOTE [J].
HAKOMORI, S ;
ANDERSON, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 203 (03) :1605-1613
[8]  
*JAP BREAST CANC S, 1996, GEN RUL CLIN PATH RE
[9]   E-SELECTIN EXPRESSION INDUCED BY PANCREAS-CARCINOMA-DERIVED INTERLEUKIN-1-ALPHA RESULTS IN ENHANCED ADHESION OF PANCREAS-CARCINOMA CELLS TO ENDOTHELIAL-CELLS [J].
KAJI, M ;
ISHIKURA, H ;
KISHIMOTO, T ;
OMI, M ;
ISHIZU, A ;
KIMURA, C ;
TAKAHASHI, T ;
KATO, H ;
YOSHIKI, T .
INTERNATIONAL JOURNAL OF CANCER, 1995, 60 (05) :712-717
[10]   ANGIOGENESIS MEDIATED BY SOLUBLE FORMS OF E-SELECTIN AND VASCULAR CELL-ADHESION MOLECULE-1 [J].
KOCH, AE ;
HALLORAN, MM ;
HASKELL, CJ ;
SHAH, MR ;
POLVERINI, PJ .
NATURE, 1995, 376 (6540) :517-519