The role of heparanase in lymph node metastatic dissemination: Dynamic contrast-enhanced MRI of Eb lymphoma in mice

被引:23
作者
Dafni, H
Cohen, B
Ziv, K
Israely, T
Goldshmidt, O
Nevo, N
Harmelin, A
Vlodavsky, I
Neeman, M [1 ]
机构
[1] Weizmann Inst Sci, Dept Biol Regulat, IL-76100 Rehovot, Israel
[2] Hadassah Hebrew Univ Hosp, Dept Oncol, IL-91120 Jerusalem, Israel
[3] Weizmann Inst Sci, Dept Vet Resources, IL-76100 Rehovot, Israel
[4] Technion Israel Inst Technol, Rappaport Family Res Inst, Tumor & Vasc Biol Res Ctr, IL-31096 Haifa, Israel
[5] Technion Israel Inst Technol, Bruce Rappaport Fac Med, IL-31096 Haifa, Israel
来源
NEOPLASIA | 2005年 / 7卷 / 03期
关键词
heparanase; vascular permeability; lymphatic drain; lymphangiography; MRI;
D O I
10.1593/neo.04433
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Heparanase expression has been linked to increased tumor invasion, metastasis, and angiogenesis and with poor prognosis. The aim of the study was to monitor the effect of heparanase expression on lymph node metastasis, in heparanase-overexpressing subcutaneous Eb mouse T-lymphoma tumors, and their draining lymph node. Dynamic contrast-enhanced magnetic resonance imaging (MRI) using biotin-BSA-GdDTPA-FAM/ROX was applied for analysis of blood volume, vascular permeability, and interstitial convection, and for detection of very early stages of such metastatic dissemination. Eb tumors increased extravasation, interstitial convection, and lymphatic drain of the contrast material. Interstitial flow directions were mapped by showing radial outflow interrupted in some tumors by directional flow toward the popliteal lymph node. Heparanase expression significantly increased contrast enhancement of the popliteal lymph node but not of the primary tumor. Changes in MR contrast enhancement preceded the formation of pathologically detectable metastases, and were detectable when only a few enhanced green fluorescent protein (EGFP)-expressing Eb cells were found near and within the nodes. These results demonstrate very early, heparanase-dependent vascular changes in lymph nodes that were visible by MRI following administration of biotin-BSA-GdDTPA-FAM/ROX, and can be used for studying the initial stages of lymph node infiltration.
引用
收藏
页码:224 / 233
页数:10
相关论文
共 39 条
[1]   Sentinel node staging of early breast cancer using lymphoscintigraphy and the intraoperative gamma-detecting probe [J].
Alazraki, NP ;
Styblo, T ;
Grant, SF ;
Cohen, C ;
Larsen, T ;
Aarsvold, JN .
SEMINARS IN NUCLEAR MEDICINE, 2000, 30 (01) :56-64
[2]   Iron oxide-enhanced MR lymphography: The evaluation of cervical lymph node metastases in head and neck cancer [J].
Anzai, Y ;
Prince, MR .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 1997, 7 (01) :75-81
[3]  
Bhujwalla ZM, 2003, CLIN CANCER RES, V9, P355
[4]   Interstitial flow as a guide for lymphangiogenesis [J].
Boardman, KC ;
Swartz, MA .
CIRCULATION RESEARCH, 2003, 92 (07) :801-808
[5]   MRI and fluorescence microscopy of the acute vascular response to VEGF165: vasodilation, hyper-permeability and lymphatic uptake, followed by rapid inactivation of the growth factor [J].
Dafni, H ;
Landsman, L ;
Schechter, B ;
Kohen, F ;
Neeman, M .
NMR IN BIOMEDICINE, 2002, 15 (02) :120-131
[6]   Modulation of the pharmacokinetics of macromolecular contrast material by avidin chase: MRI, optical, and inductively coupled plasma mass spectrometry tracking of triply labeled albumin [J].
Dafni, H ;
Gilead, A ;
Nevo, N ;
Eilam, R ;
Harmelin, A ;
Neeman, M .
MAGNETIC RESONANCE IN MEDICINE, 2003, 50 (05) :904-914
[7]  
Dafni H, 2002, CANCER RES, V62, P6731
[8]   Macromolecular contrast agents for MR mammography: current status [J].
Daldrup-Link, HE ;
Brasch, RC .
EUROPEAN RADIOLOGY, 2003, 13 (02) :354-365
[9]   Expression of heparanase in normal, dysplastic, and neoplastic human colonic mucosa and stroma -: Evidence for its role in colonic tumorigenesis [J].
Friedmann, Y ;
Vlodavsky, I ;
Aingorn, H ;
Aviv, A ;
Peretz, T ;
Pecker, I ;
Pappo, O .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (04) :1167-1175
[10]   Cell surface expression and secretion of heparanase markedly promote tumor angiogenesis and metastasis [J].
Goldshmidt, O ;
Zcharia, E ;
Abramovitch, R ;
Metzger, S ;
Aingorn, H ;
Friedmann, Y ;
Schirrmacher, V ;
Mitrani, E ;
Vlodavsky, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (15) :10031-10036