Expression of delta-like ligand 4 (Dll4) and markers of hypoxia in colon cancer

被引:95
作者
Jubb, A. M. [1 ]
Turley, H. [1 ]
Moeller, H. C. [1 ]
Steers, G. [1 ]
Han, C. [2 ]
Li, J-L [2 ]
Leek, R. [1 ]
Tan, E. Y. [1 ]
Singh, B. [3 ]
Mortensen, N. J. [3 ]
Noguera-Troise, I. [4 ]
Pezzella, F. [1 ]
Gatter, K. C. [1 ]
Thurston, G. [4 ]
Fox, S. B. [5 ]
Harris, A. L. [1 ]
机构
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Lab Sci, Oxford OX3 9DS, England
[2] Univ Oxford, John Radcliffe Hosp, Weatherall Inst Mol Med, Oxford OX3 9DS, England
[3] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Surg, Oxford OX3 9DU, England
[4] Regeneron Pharmaceut, Tarrytown, NY 10591 USA
[5] Peter MacCallum Canc Ctr, Dept Pathol, Melbourne, Vic 3002, Australia
关键词
delta-like ligand 4; colon cancer; hypoxia; angiogenesis; survival; ENDOTHELIAL GROWTH-FACTOR; METASTATIC COLORECTAL-CANCER; CARBONIC-ANHYDRASE-IX; IN-SITU HYBRIDIZATION; INHIBITS TUMOR-GROWTH; INDUCIBLE FACTOR-1-ALPHA; UP-REGULATION; PROLYL HYDROXYLASES; MICROVESSEL DENSITY; ANGIOGENIC SWITCH;
D O I
10.1038/sj.bjc.6605368
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Delta-like ligand 4 (Dll4) is a Notch ligand that is upregulated by hypoxia and vascular endothelial growth factor-A (VEGF-A) and is reported to have a role in tumor angiogenesis. Evidence from xenograft studies suggests that inhibiting Dll4-Notch signalling may overcome resistance to anti-VEGF therapy. The aim of this study was to characterise the expression of Dll4 in colon cancer and to assess whether it is associated with markers of hypoxia and prognosis. METHOD: In all, 177 colon cancers were represented in tissue microarrays. Immunohistochemistry was performed using validated antibodies against Dll4, VEGF, hypoxia-inducible factor (HIF)-1 alpha, HIF-2 alpha, prolyl hydroxylase (PHD) 1, PHD2, PHD3 and carbonic anhydrase 9 (CA9). RESULTS: The expression of Dll4 was observed preferentially in the endothelium of 71% (125 out of 175) of colon cancers, but not in the endothelium adjacent to normal mucosa (none out of 107, P<0.0001). The expression of VEGF was significantly associated with HIF-2 alpha (P<0.0001) and Dll4 (P = 0.010). Only HIF-2 alpha had a significant multivariate prognostic effect (hazard ratio 1.61, 95% confidence interval 1.01-2.57). Delta-like ligand 4 was also expressed by neoplastic cells, particularly neoplastic goblet cells. CONCLUSION: Endothelial expression of Dll4 is not a prognostic factor, but is significantly associated with VEGF. Assessing endothelial Dll4 expression may be critical in predicting response to anti-VEGF therapies. British Journal of Cancer (2009) 101, 1749-1757. doi: 10.1038/sj.bjc.6605368 www.bjcancer.com Published online 20 October 2009 (C) 2009 Cancer Research UK
引用
收藏
页码:1749 / 1757
页数:9
相关论文
共 61 条
  • [1] Tumor morphology and phenotypic evolution driven by selective pressure from the microenvironment
    Anderson, Alexander R. A.
    Weaver, Alissa M.
    Cummings, Peter T.
    Quaranta, Vito
    [J]. CELL, 2006, 127 (05) : 905 - 915
  • [2] Differential function of the prolyl hydroxylases PHD1, PHD2, and PHD3 in the regulation of hypoxia-inducible factor
    Appelhoff, RJ
    Tian, YM
    Raval, RR
    Turley, H
    Harris, AL
    Pugh, CW
    Ratcliffe, PJ
    Gleadle, JM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (37) : 38458 - 38465
  • [3] CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING
    BENJAMINI, Y
    HOCHBERG, Y
    [J]. JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) : 289 - 300
  • [4] Effects of angiogenesis inhibitors on multistage carcinogenesis in mice
    Bergers, G
    Javaherian, K
    Lo, KM
    Folkman, J
    Hanahan, D
    [J]. SCIENCE, 1999, 284 (5415) : 808 - 812
  • [5] The androgen receptor is significantly associated with vascular endothelial growth factor and hypoxia sensing via hypoxia-inducible factors HIF-1a, HIF-2a, and the prolyl hydroxylases in human prostate cancer
    Boddy, JL
    Fox, SB
    Han, C
    Campo, L
    Turley, H
    Kanga, S
    Malone, PR
    Harris, AL
    [J]. CLINICAL CANCER RESEARCH, 2005, 11 (21) : 7658 - 7663
  • [6] Tissue microarray (TMA) technology:: miniaturized pathology archives for high-throughput in situ studies
    Bubendorf, L
    Nocito, A
    Moch, H
    Sauter, G
    [J]. JOURNAL OF PATHOLOGY, 2001, 195 (01) : 72 - 79
  • [7] Blocking neuropilin-2 function inhibits tumor cell metastasis
    Caunt, Maresa
    Mak, Judy
    Liang, Wei-Ching
    Stawicki, Scott
    Pan, Qi
    Tong, Raymond K.
    Kowalski, Joe
    Ho, Calvin
    Reslan, Hani Bou
    Ross, Jed
    Berry, Leanne
    Kasman, Ian
    Zlot, Constance
    Cheng, Zhiyong
    Le Couter, Jennifer
    Filvaroff, Ellen H.
    Plowman, Greg
    Peale, Franklin
    French, Dorothy
    Carano, Richard
    Koch, Alexander W.
    Wu, Yan
    Watts, Ryan J.
    Tessier-Lavigne, Marc
    Bagri, Anil
    [J]. CANCER CELL, 2008, 13 (04) : 331 - 342
  • [8] Cleven AHG, 2007, CELL ONCOL, V29, P229
  • [9] Hypoxia up-regulates prolyl hydroxylase activity - A feedback mechansim that limits HIF-1 responses during reoxygenation
    D'Angelo, G
    Duplan, E
    Boyer, N
    Vigne, P
    Frelin, C
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (40) : 38183 - 38187
  • [10] Dosage-sensitive requirement for mouse D114 in artery development
    Duarte, A
    Hirashima, M
    Benedito, R
    Trindade, A
    Diniz, P
    Bekman, E
    Costa, L
    Henrique, D
    Rossant, J
    [J]. GENES & DEVELOPMENT, 2004, 18 (20) : 2474 - 2478