Selective Visualization of Cyclooxygenase-2 in Inflammation and Cancer by Targeted Fluorescent Imaging Agents

被引:144
作者
Uddin, Md. Jashim [3 ,4 ]
Crews, Brenda C. [3 ,4 ]
Blobaum, Anna L. [3 ,4 ]
Kingsley, Philip J. [3 ,4 ]
Gorden, D. Lee [5 ]
McIntyre, J. Oliver [5 ]
Matrisian, Lynn M. [5 ]
Subbaramaiah, Kotha [6 ]
Dannenberg, Andrew J. [6 ]
Piston, David W. [1 ,2 ]
Marnett, Lawrence J. [1 ,3 ,4 ]
机构
[1] Vanderbilt Univ, Med Ctr, Sch Med, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Phys & Astron, Sch Med, Nashville, TN 37232 USA
[3] Vanderbilt Inst Chem Biol, AB Hancock Jr Mem Lab Canc Res, Dept Biochem, Ctr Mol Toxicol, Nashville, TN USA
[4] Vanderbilt Inst Chem Biol, AB Hancock Jr Mem Lab Canc Res, Dept Chem & Pharmacol, Ctr Mol Toxicol, Nashville, TN USA
[5] Vanderbilt Ingram Canc Ctr, Dept Canc Biol, Nashville, TN USA
[6] Cornell Univ, Weill Med Coll, Dept Med, New York, NY 10021 USA
关键词
GROWTH-FACTOR RECEPTOR; IN-VIVO EVALUATION; HUMAN COLON-CANCER; SUBCELLULAR-LOCALIZATION; COX-2; EXPRESSION; PET TRACER; INHIBITION; SYNTHASE-1; PROTEIN; TUMORS;
D O I
10.1158/0008-5472.CAN-09-2664
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Effective diagnosis of inflammation and cancer by molecular imaging is challenging because of interference from nonselective accumulation of the contrast agents in normal tissues. Here, we report a series of novel fluorescence imaging agents that efficiently target cyclooxygenase-2 (COX-2), which is normally absent from cells, but is found at high levels in inflammatory lesions and in many premalignant and malignant tumors. After either i.p. or i.v. injection, these reagents become highly enriched in inflamed or tumor tissue compared with normal tissue and this accumulation provides sufficient signal for in vivo fluorescence imaging. Further, we show that only the intact parent compound is found in the region of interest. COX-2-specific delivery was unambiguously confirmed using animals bearing targeted deletions of COX-2 and by blocking the COX-2 active site with high-affinity inhibitors in both in vitro and in vivo models. Because of their high specificity, contrast, and detectability, these fluorocoxibs are ideal candidates for detection of inflammatory lesions or early-stage COX-2-expressing human cancers, such as those in the esophagus, oropharynx, and colon. Cancer Res; 70(9); 3618-27. (C) 2010 AACR.
引用
收藏
页码:3618 / 3627
页数:10
相关论文
共 39 条
  • [11] Eicosanoid modulation in advanced lung cancer: Cyclooxygenase-2 expression is a positive predictive factor for celecoxib plus chemotherapy - Cancer and leukemia group B trial 30203
    Edelman, Martin J.
    Watson, Dee
    Wang, Xiaofei
    Morrison, Carl
    Kratzke, Robert A.
    Jewell, Scott
    Hodgson, Lydia
    Mauer, Ann M.
    Gajra, Ajeet
    Masters, Gregory A.
    Bedor, Michelle
    Vokes, Everett E.
    Green, Mark J.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (06) : 848 - 855
  • [12] Sturctural basis of enantioselective inhibition of cyclooxygenase-1 S-α-Substituted indomethacin ethanolamides
    Harman, Christine A.
    Turman, Melissa V.
    Kozak, Kevin R.
    Marnett, Lawrence J.
    Smith, William L.
    Garavito, R. Michael
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (38) : 28096 - 28105
  • [13] Jacoby RF, 2000, CANCER RES, V60, P5040
  • [14] Biochemically based design of cyclooxygenase-2 (COX-2) inhibitors: Facile conversion of nonsteroidal antiinflammatory drugs to potent and highly selective COX-2 inhibitors
    Kalgutkar, AS
    Crews, BC
    Rowlinson, SW
    Marnett, AB
    Kozak, KR
    Remmel, RP
    Marnett, LJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (02) : 925 - 930
  • [15] Cyclooxygenase-2 expression in Barrett's esophagus
    Kandil, HM
    Tanner, G
    Smalley, W
    Halter, S
    Radhika, A
    Dubois, RN
    [J]. DIGESTIVE DISEASES AND SCIENCES, 2001, 46 (04) : 785 - 789
  • [16] KARGMAN SL, 1995, CANCER RES, V55, P2556
  • [17] Structural basis for selective inhibition of cyclooxygenase-2 by anti-inflammatory agents
    Kurumbail, RG
    Stevens, AM
    Gierse, JK
    McDonald, JJ
    Stegeman, RA
    Pak, JY
    Gildehaus, D
    Miyashiro, JM
    Penning, TD
    Seibert, K
    Isakson, PC
    Stallings, WC
    [J]. NATURE, 1996, 384 (6610) : 644 - 648
  • [18] Cyclooxygenase enzymes: catalysis and inhibition
    Kurumbail, RG
    Kiefer, JR
    Marnett, LJ
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 2001, 11 (06) : 752 - 760
  • [19] Flexibility of the NSAID binding site in the structure of human cyclooxygenase-2
    Luong, C
    Miller, A
    Barnett, J
    Chow, J
    Ramesha, C
    Browner, MF
    [J]. NATURE STRUCTURAL BIOLOGY, 1996, 3 (11): : 927 - 933
  • [20] A general method for the synthesis of aryl [11C]methylsulfones:: Potential PET probes for imaging cyclooxygenase-2 expression
    Majo, VJ
    Prabhakaran, J
    Simpson, NR
    Van Heertum, RL
    Mann, JJ
    Kumar, JSD
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2005, 15 (19) : 4268 - 4271