Lymphatic vasculature: development, molecular regulation and role in tumor metastasis and inflammation

被引:332
作者
Saharinen, P
Tammela, T
Karkkainen, MJ
Alitalo, K
机构
[1] Univ Helsinki, Mol Canc Biol Lab, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Ludwig Inst Canc Res, Biomed Helsinki, FIN-00014 Helsinki, Finland
[3] Univ Helsinki, Univ Cent Hosp, FIN-00014 Helsinki, Finland
关键词
D O I
10.1016/j.it.2004.05.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The lymphatic vascular system is important for immune surveillance, tissue fluid homeostasis and fat absorption, and is involved in many pathological processes, including tumor metastasis and lymphedema. The recent success in the isolation of lymphatic endothelial cells has shed light on their molecular characteristics. Lymphatic commitment and growth during embryonic development is dependent on the activities of the homeodomain transcription factor Prox-1 and vascular endothelial growth factor-C (VEGF-C). VEGF-C and VEGF-D are involved in adult inflammation-associated lymphangiogenesis, wound healing and tumor metastasis. Administration of lymphangiogenic growth factors or their antagonists provides the possibility of targeting lymphatic vessels in human disease.
引用
收藏
页码:387 / 395
页数:9
相关论文
共 88 条
[11]   THE INHERITANCE OF PRIMARY LYMPHOEDEMA [J].
DALE, RF .
JOURNAL OF MEDICAL GENETICS, 1985, 22 (04) :274-278
[12]   Ligand-induced vascular endothelial growth factor receptor-3 (VEGFR-3) heterodimerization with VEGFR-2 in primary lymphatic endothelial cells regulates tyrosine phosphorylation sites [J].
Dixelius, J ;
Mäkinen, T ;
Wirzenius, M ;
Karkkainen, MJ ;
Wernstedt, C ;
Alitalo, K ;
Claesson-Welsh, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (42) :40973-40979
[13]   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
[14]   Comparison of VEGF, VEGF-B, VEGF-C and Ang-1 mRNA regulation by serum, growth factors, oncoproteins and hypoxia [J].
Enholm, B ;
Paavonen, K ;
Ristimaki, A ;
Kumar, V ;
Gunji, Y ;
Klefstrom, J ;
Kivinen, L ;
Laiho, M ;
Olofsson, B ;
Joukov, V ;
Eriksson, U ;
Alitalo, K .
ONCOGENE, 1997, 14 (20) :2475-2483
[15]   Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome [J].
Fang, JM ;
Dagenais, SL ;
Erickson, RP ;
Arlt, MF ;
Glynn, MW ;
Gorski, JL ;
Seaver, LH ;
Glover, TW .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (06) :1382-1388
[16]  
Galetti TP, 2002, EUR UROL SUPPL, V1, P3
[17]   Novel expression of vascular endothelial growth factor receptor (VEGFR)-3 and VEGF-C on corneal dendritic cells [J].
Hamrah, P ;
Chen, L ;
Zhang, Q ;
Dana, MR .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 163 (01) :57-68
[18]   Suppression of tumor lymphangiogenesis and lymph node metastasis by blocking vascular endothelial growth factor receptor 3 signaling [J].
He, YL ;
Kozaki, KI ;
Karpanen, T ;
Koshikawa, K ;
Yla-Herttuala, S ;
Takahashi, T ;
Alitalo, K .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2002, 94 (11) :819-825
[19]   Identification of vascular lineage-specific genes by transcriptional profiling of isolated blood vascular and lymphatic endothelial cells [J].
Hirakawa, S ;
Hong, YK ;
Harvey, N ;
Schacht, V ;
Matsuda, K ;
Libermann, T ;
Detmar, M .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 162 (02) :575-586
[20]   Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations [J].
Hong, SE ;
Shugart, YY ;
Huang, DT ;
Shahwan, SA ;
Grant, PE ;
Hourihane, JOB ;
Martin, NDT ;
Walsh, CA .
NATURE GENETICS, 2000, 26 (01) :93-96