Lymphangiogenesis and the vascular endothelial growth factor receptor (VEGFR)-3 in gastric cancer

被引:323
作者
Yonemura, Y
Fushida, S
Bando, E
Kinoshita, K
Miwa, K
Endo, Y
Sugiyama, K
Partanen, T
Yamamoto, H
Sasaki, T
机构
[1] Kanazawa Univ, Sch Med, Dept Surg 2, Kanazawa, Ishikawa 920, Japan
[2] Kanazawa Univ, Expt Therapeut Canc Res Inst, Kanazawa, Ishikawa 920, Japan
[3] Natl Canc Ctr, Res Inst, Div Virol, Chuo Ku, Tokyo 104, Japan
[4] Univ Helsinki, Haartman Inst, Mol Canc Biol Lab, FIN-00014 Helsinki, Finland
[5] Kanazawa Univ, Sch Med, Dept Biochem, Kanazawa, Ishikawa 920, Japan
关键词
VTGF-C; VEGFR-3; gastric cancer; Flt4; lymphangiogenesis;
D O I
10.1016/S0959-8049(01)00015-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Vascular endothelial growth factor C (VEGF-C) is the only factor known to cause lymphangiogenesis. We studied the correlation between VEGF-C and vascular endothelial growth factor receptor-3 (VEGFR-3) expression of 85 primary gastric cancers by reverse transcriptase-polymerase chain reaction (RT-PCR) and immunohistochemistry, and the results were correlated with the number of lymphatic vessels, stained with anti-VEGFR-3 antibody. RT-PCR and immunohistology demonstrated that VEGF-C was mainly produced from cancer cells. but not from stromal elements. Morphologically, VEGFR-3 expression was detected in the endothelial cells of the stromal lymphatic vessels. There was a statistically positive correlation between the incidence of VEGF-C and VEGFR-3 mRNA expression in the primary tumours (P=0.0002). The number of VEGFR-3-positive lymphatic vessels in VEGF-C mRNA positive tumours was significantly larger than that in VEGF-C-negative tumours. The number of VEGFR-3-positive vessels in the tumour stroma was closely related to the grade of lymphatic invasion of gastric cancer. These results strongly indicate that VEGF-C may induce the proliferation of lymphatic vessels in the stroma of primary gastric cancer via activation of VEGFR-3, expressed on the endothelial cells of lymphatic vessels. In these circumstances. cancer cells can easily invade the lymphatic vessel. because of the increase of the contact points of cancer cells with the lymphatic vessels. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:918 / 923
页数:6
相关论文
共 23 条
[1]
VASCULAR ENDOTHELIAL GROWTH-FACTOR ACTS AS A SURVIVAL FACTOR FOR NEWLY FORMED RETINAL-VESSELS AND HAS IMPLICATIONS FOR RETINOPATHY OF PREMATURITY [J].
ALON, T ;
HEMO, I ;
ITIN, A ;
PEER, J ;
STONE, J ;
KESHET, E .
NATURE MEDICINE, 1995, 1 (10) :1024-1028
[2]
In vivo angiogenic activity and hypoxia induction of heterodimers of placenta growth factor vascular endothelial growth factor [J].
Cao, YH ;
Linden, P ;
Shima, D ;
Browne, F ;
Folkman, J .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (11) :2507-2511
[3]
SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[4]
MULTIPLE PROTEIN-4.1 ISOFORMS PRODUCED BY ALTERNATIVE SPLICING IN HUMAN ERYTHROID-CELLS [J].
CONBOY, JG ;
CHAN, J ;
MOHANDAS, N ;
KAN, YW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) :9062-9065
[5]
The placenta growth factor gene of the mouse [J].
DiPalma, T ;
Tucci, M ;
Russo, G ;
Maglione, D ;
Lago, CT ;
Romano, A ;
Saccone, S ;
DellaValle, G ;
DeGregorio, L ;
Dragani, TA ;
Viglietto, G ;
Persico, MG .
MAMMALIAN GENOME, 1996, 7 (01) :6-12
[6]
Cardiovascular failure in mouse embryos deficient in VEGF receptor-3 [J].
Dumont, DJ ;
Jussila, L ;
Taipale, J ;
Lymboussaki, A ;
Mustonen, T ;
Pajusola, K ;
Breitman, M ;
Alitalo, K .
SCIENCE, 1998, 282 (5390) :946-949
[7]
DVORAK HF, 1995, AM J PATHOL, V146, P1029
[8]
*JAP RES SOC GASTR, 1993, JAP CLASS GASTR CANC
[9]
Hyperplasia of lymphatic vessels in VEGF-C transgenic mice [J].
Jeltsch, M ;
Kaipainen, A ;
Joukov, V ;
Meng, XJ ;
Lakso, M ;
Rauvala, H ;
Swartz, M ;
Fukumura, D ;
Jain, RK ;
Alitalo, K .
SCIENCE, 1997, 276 (5317) :1423-1425
[10]
Joukov V, 1996, EMBO J, V15, P290