The hypoxia-inducible genes VEGF and CA9 are differentially regulated in superficial vs invasive bladder cancer

被引:104
作者
Turner, KJ
Crew, JP
Wykoff, CC
Watson, PH
Poulsom, R
Pastorek, J
Ratcliffe, PJ
Cranston, D
Harris, AL [1 ]
机构
[1] John Radcliffe Hosp, Weatherall Inst Mol Med, ICRF Mol Oncol Grp, Oxford OX3 9DS, England
[2] John Radcliffe Hosp, Weatherall Inst Mol Med, ICRF Mol Oncol Lab, Oxford OX3 9DS, England
[3] John Radcliffe Hosp, Weatherall Inst Mol Med, Angiogenesis Grp, Oxford OX3 9DS, England
[4] Univ Manitoba, Dept Pathol, Winnipeg, MB R3E 0W3, Canada
[5] ICRF, Situ Hybridisat Serv, London WC2A 3PX, England
[6] Slovak Acad Sci, Inst Virol, Bratislava, Slovakia
[7] Wellcome Trust Ctr Human Genet, Oxford 0X3 7BN, England
关键词
bladder neoplasms; angiogenic factors; carbonic acid; cell hypoxia;
D O I
10.1038/sj.bjc.6600215
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Regulation by hypoxia may underlie the expression of vascular endothelial growth factor in bladder cancer. We have compared the distribution of vascular endothelial growth factor mRNA with a hypoxia marker, carbonic anhydrase 9 (CA IX). vascular endothelial growth factor mRNA was analysed by In situ hybridisation and CA IX by immunochemistry in 22 cases of bladder cancer, The relationship of microvessels to the distribution of CA IX was determined, In a separate series of 49 superficial tumours, CA IX immunostaining was compared with clinico-pathological outcome In superficial and invasive disease there was overlap in the expression of vascular endothelial growth factor and CA IX CA IX being more widespread. Both were expressed predominantly on the luminal surface, and surrounding areas of necrosis (invasive tumours), Expression of both factors was greater in superficial disease. Expression was absent within similar to80 mum of microvessels, Unlike vascular endothelial growth factor, CA IX did not predict outcome in superficial disease, Differential responses to reoxygenation provide one explanation: vascular endothelial growth factor mRNA declined rapidly. while CA IX expression was sustained for >72 h. Expression of vascular endothelial growth factor mRNA in bladder tumours is consistent with hypoxic regulation and suggests differential regulation in superficial vs invasive disease. The expression of CA IX on the luminal-surface justifies investigation of its utility as a therapeutic target/prognosbc indicator. (C) 2002 Cancer Research UK.
引用
收藏
页码:1276 / 1282
页数:7
相关论文
共 27 条
  • [1] ANGIOGENESIS IN BLADDER-CANCER - RELATIONSHIP BETWEEN MICROVESSEL DENSITY AND TUMOR PROGNOSIS
    BOCHNER, BH
    COTE, RJ
    WEIDNER, N
    GROSHEN, S
    CHEN, SC
    SKINNER, DG
    NICHOLS, PW
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (21) : 1603 - 1612
  • [2] Borgström P, 1998, PROSTATE, V35, P1
  • [3] Brizel DM, 1996, CANCER RES, V56, P941
  • [4] Urinary vascular endothelial growth factor and its correlation with bladder cancer recurrence rates - Reply
    Crew, JP
    O'Brien, T
    Bicknell, R
    Fuggle, S
    Cranston, D
    Harris, AL
    [J]. JOURNAL OF UROLOGY, 1999, 161 (03) : 804 - 804
  • [5] Crew JP, 1997, CANCER RES, V57, P5281
  • [6] Crew JP, 2000, BRIT J CANCER, V82, P161
  • [7] Isoenzyme-specific regulation of genes involved in energy metabolism by hypoxia: Similarities with the regulation of erythropoietin
    Ebert, BL
    Gleadle, JM
    ORourke, JF
    Bartlett, SM
    Poulton, J
    Ratcliffe, PJ
    [J]. BIOCHEMICAL JOURNAL, 1996, 313 : 809 - 814
  • [8] The biology of vascular endothelial growth factor
    Ferrara, N
    DavisSmyth, T
    [J]. ENDOCRINE REVIEWS, 1997, 18 (01) : 4 - 25
  • [9] OXYGEN-REGULATED CONTROL ELEMENTS IN THE PHOSPHOGLYCERATE KINASE-1 AND LACTATE-DEHYDROGENASE-A GENES - SIMILARITIES WITH THE ERYTHROPOIETIN 3' ENHANCER
    FIRTH, JD
    EBERT, BL
    PUGH, CW
    RATCLIFFE, PJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) : 6496 - 6500
  • [10] WHAT IS THE EVIDENCE THAT TUMORS ARE ANGIOGENESIS DEPENDENT
    FOLKMAN, J
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1990, 82 (01): : 4 - 6