Antiangiogenic agents are effective inhibitors of endometriosis

被引:213
作者
Hull, ML
Charnock-Jones, DS
Chan, CLK
Bruner-Tran, KL
Osteen, KG
Tom, BDM
Fan, TPD
Smith, SK
机构
[1] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
[2] Univ Cambridge, Dept Obstet & Gynecol, Cambridge CB2 1QP, England
[3] Univ Cambridge, Dept Pharmacol, Cambridge CB2 1QP, England
[4] Univ Cambridge, Reprod Mol Res Grp, Cambridge CB2 1QP, England
[5] Vanderbilt Univ, Womens Reprod Hlth Res Ctr, Nashville, TN 37232 USA
[6] Inst Publ Hlth, MRC, Biostat Unit, Cambridge CB2 2SR, England
关键词
D O I
10.1210/jc.2002-021912
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Endometriosis is a disease in which the lining of the uterus ( endometrium), shed at the time of menstruation, becomes established at sites such as the peritoneum and ovaries. These explants develop a rich blood supply that enables them to survive and grow. We hypothesized that inhibitors of angiogenesis would prevent this growth by disrupting sensitive vessels supplying endometriotic lesions. Vessels sensitive to angiogenic antagonism have few associations with pericyte cells. The vessels supplying human endometriotic lesions were immunohistochemically characterized and found to be predominantly pericyte free. A model in which human endometrium is implanted into nude mice was used to test the effects of two antagonists of the angiogenic growth factor, vascular endothelial cell growth factor A. Soluble truncated receptor ( flt- 1; P = 0.002) and an affinity- purified antibody to human vascular endothelial cell growth factor A ( P = 0.03) significantly inhibited the growth of nude mouse explants. Pericyte- free vessels were shown to supply endometrial lesions in nude mice and were disrupted in lesions taken from soluble flt- 1- treated mice. In summary, antiangiogenic agents inhibited the growth of explants in an in vivo model of endometriosis by disrupting the vascular supply, and this effect is likely to apply to the human disease. These findings suggest that antiangiogenic agents may provide a novel therapeutic approach for the treatment of endometriosis.
引用
收藏
页码:2889 / 2899
页数:11
相关论文
共 37 条
[1]   Selective ablation of immature blood vessels in established human tumors follows vascular endothelial growth factor withdrawal [J].
Benjamin, LE ;
Golijanin, D ;
Itin, A ;
Pode, D ;
Keshet, E .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (02) :159-165
[2]  
Benjamin LE, 1998, DEVELOPMENT, V125, P1591
[3]   Suppression of matrix metalloproteinases inhibits establishment of ectopic lesions by human endometrium in nude mice [J].
Bruner, KL ;
Matrisian, LM ;
Rodgers, WH ;
Gorstein, F ;
Osteen, KG .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (12) :2851-2857
[4]   Mechanisms of angiogenesis and arteriogenesis [J].
Carmeliet, P .
NATURE MEDICINE, 2000, 6 (04) :389-395
[5]   IDENTIFICATION AND LOCALIZATION OF ALTERNATELY SPLICED MESSENGER-RNAS FOR VASCULAR ENDOTHELIAL GROWTH-FACTOR IN HUMAN UTERUS AND ESTROGEN REGULATION IN ENDOMETRIAL CARCINOMA CELL-LINES [J].
CHARNOCKJONES, DS ;
SHARKEY, AM ;
RAJPUTWILLIAMS, J ;
BURCH, D ;
SCHOFIELD, JP ;
FOUNTAIN, SA ;
BOOCOCK, CA ;
SMITH, SK .
BIOLOGY OF REPRODUCTION, 1993, 48 (05) :1120-1128
[6]   Heterozygous embryonic lethality induced by targeted inactivation of the VEGF gene [J].
Ferrara, N ;
CarverMoore, K ;
Chen, H ;
Dowd, M ;
Lu, L ;
OShea, KS ;
PowellBraxton, L ;
Hillan, KJ ;
Moore, MW .
NATURE, 1996, 380 (6573) :439-442
[7]   ROLE OF THE FLT-1 RECEPTOR TYROSINE KINASE IN REGULATING THE ASSEMBLY OF VASCULAR ENDOTHELIUM [J].
FONG, GH ;
ROSSANT, J ;
GERTSENSTEIN, M ;
BREITMAN, ML .
NATURE, 1995, 376 (6535) :66-70
[8]   Vascular endothelial growth factor induces expression of the antiapoptotic proteins Bcl-2 and A1 in vascular endothelial cells [J].
Gerber, HP ;
Dixit, V ;
Ferrara, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (21) :13313-13316
[9]   Vascular endothelial growth factor regulates endothelial cell survival through the phosphatidylinositol 3′-kinase Akt signal transduction pathway -: Requirement for Flk-1/KDR activation [J].
Gerber, HP ;
McMurtrey, A ;
Kowalski, J ;
Yan, MH ;
Keyt, BA ;
Dixit, V ;
Ferrara, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (46) :30336-30343
[10]   Peritoneal endometriosis:: validation of an in-vivo model [J].
Grümmer, R ;
Schwarzer, F ;
Bainczyk, K ;
Hess-Stumpp, H ;
Regidor, PA ;
Schindler, AE ;
Winterhager, E .
HUMAN REPRODUCTION, 2001, 16 (08) :1736-1743