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Volumn 18, Issue 3, 2016, Pages 393-401

Comparison of [11C]Choline ([11C]CHO) and [18F]Bombesin (BAY 86-4367) as Imaging Probes for Prostate Cancer in a PC-3 Prostate Cancer Xenograft Model

Author keywords

Bombesin; Choline; Prostate cancer; Small animal PET CT; Xenograft mouse model

Indexed keywords

BOMBESIN F 18; CHOLINE C 11; GASTRIN RELEASING PEPTIDE RECEPTOR; RADIOPHARMACEUTICAL AGENT; UNCLASSIFIED DRUG; BAY 86-4367; BOMBESIN; CARBON; CHOLINE; FLUORINE; MOLECULAR PROBE;

EID: 84944684934     PISSN: 15361632     EISSN: 18602002     Source Type: Journal    
DOI: 10.1007/s11307-015-0901-1     Document Type: Article
Times cited : (2)

References (32)
  • 1
    • 0036282024 scopus 로고    scopus 로고
    • Comparison of [18 F]fluorocholine and [18 F]fluorodeoxyglucose for positron emission tomography of androgen dependent and androgen independent prostate cancer
    • PID: 12050555
    • Price DT, Coleman RE, Liao RP et al (2002) Comparison of [18 F]fluorocholine and [18 F]fluorodeoxyglucose for positron emission tomography of androgen dependent and androgen independent prostate cancer. J Urol 168:273–280
    • (2002) J Urol , vol.168 , pp. 273-280
    • Price, D.T.1    Coleman, R.E.2    Liao, R.P.3
  • 2
    • 2442536830 scopus 로고    scopus 로고
    • [11C]Choline as a PET biomarker for assessment of prostate cancer tumor models
    • COI: 1:CAS:528:DC%2BD2cXktVKqtrk%3D, PID: 15142549
    • Zheng QH, Gardner TA, Raikwar S et al (2004) [11C]Choline as a PET biomarker for assessment of prostate cancer tumor models. Bioorg Med Chem 12:2887–2893
    • (2004) Bioorg Med Chem , vol.12 , pp. 2887-2893
    • Zheng, Q.H.1    Gardner, T.A.2    Raikwar, S.3
  • 3
    • 0037203980 scopus 로고    scopus 로고
    • Regulation of choline kinase activity by Ras proteins involves Ral-GDS and PI3K
    • COI: 1:CAS:528:DC%2BD38Xhtl2ktbw%3D, PID: 11840339
    • Ramirez de Molina A, Penalva V, Lucas L, Lacal JC (2002) Regulation of choline kinase activity by Ras proteins involves Ral-GDS and PI3K. Oncogene 21:937–946
    • (2002) Oncogene , vol.21 , pp. 937-946
    • Ramirez de Molina, A.1    Penalva, V.2    Lucas, L.3    Lacal, J.C.4
  • 4
    • 0036385709 scopus 로고    scopus 로고
    • Overexpression of choline kinase is a frequent feature in human tumor-derived cell lines and in lung, prostate, and colorectal human cancers
    • COI: 1:CAS:528:DC%2BD38XmtFShtb8%3D, PID: 12176020
    • Ramirez de Molina A, Rodriguez-Gonzalez A, Gutierrez R et al (2002) Overexpression of choline kinase is a frequent feature in human tumor-derived cell lines and in lung, prostate, and colorectal human cancers. Biochem Biophys Res Commun 296:580–583
    • (2002) Biochem Biophys Res Commun , vol.296 , pp. 580-583
    • Ramirez de Molina, A.1    Rodriguez-Gonzalez, A.2    Gutierrez, R.3
  • 5
    • 33846430535 scopus 로고    scopus 로고
    • Choline transporter as a novel target for molecular imaging of cancer
    • PID: 17150162
    • Hara T, Bansal A, DeGrado TR (2006) Choline transporter as a novel target for molecular imaging of cancer. Mol Imaging 5:498–509
    • (2006) Mol Imaging , vol.5 , pp. 498-509
    • Hara, T.1    Bansal, A.2    DeGrado, T.R.3
  • 6
    • 0030017723 scopus 로고    scopus 로고
    • Kinetics of choline transport and phosphorylation in human breast cancer cells; NMR application of the zero trans method
    • COI: 1:CAS:528:DyaK28XkslWjt7o%3D, PID: 8694504
    • Katz-Brull R, Degani H (1996) Kinetics of choline transport and phosphorylation in human breast cancer cells; NMR application of the zero trans method. Anticancer Res 16:1375–1380
    • (1996) Anticancer Res , vol.16 , pp. 1375-1380
    • Katz-Brull, R.1    Degani, H.2
  • 7
    • 84924548772 scopus 로고    scopus 로고
    • Comparison of [(11)C]choline ([(11)C]CHO) and S(+)-beta-methyl-[(11)C]choline ([(11)C]SMC) as imaging probes for prostate cancer in a PC-3 prostate cancer xenograft model
    • Schwarzenboeck SM, Gertz J, Souvatzoglou M et al (2015) Comparison of [(11)C]choline ([(11)C]CHO) and S(+)-beta-methyl-[(11)C]choline ([(11)C]SMC) as imaging probes for prostate cancer in a PC-3 prostate cancer xenograft model. Mol Imaging Biol 17:248–256
    • (2015) Mol Imaging Biol , vol.17 , pp. 248-256
    • Schwarzenboeck, S.M.1    Gertz, J.2    Souvatzoglou, M.3
  • 8
    • 0033104343 scopus 로고    scopus 로고
    • Gastrin-releasing peptide receptors in the human prostate: relation to neoplastic transformation
    • COI: 1:CAS:528:DyaK1MXhslertrc%3D, PID: 10070977
    • Markwalder R, Reubi JC (1999) Gastrin-releasing peptide receptors in the human prostate: relation to neoplastic transformation. Cancer Res 59:1152–1159
    • (1999) Cancer Res , vol.59 , pp. 1152-1159
    • Markwalder, R.1    Reubi, J.C.2
  • 9
    • 79851506832 scopus 로고    scopus 로고
    • 18F-labeled bombesin analog for specific and effective targeting of prostate tumors expressing gastrin-releasing peptide receptors
    • COI: 1:CAS:528:DC%2BC3MXisF2ku7g%3D, PID: 21233180
    • Honer M, Mu L, Stellfeld T et al (2011) 18F-labeled bombesin analog for specific and effective targeting of prostate tumors expressing gastrin-releasing peptide receptors. J Nucl Med 52:270–278
    • (2011) J Nucl Med , vol.52 , pp. 270-278
    • Honer, M.1    Mu, L.2    Stellfeld, T.3
  • 10
    • 84886737224 scopus 로고    scopus 로고
    • Synthesis and radiopharmacological evaluation of (6)(4)Cu-labeled bombesin analogs featuring a bis(2-pyridylmethyl)-1,4,7-triazacyclononane chelator
    • COI: 1:CAS:528:DC%2BC3sXhvFOqu7zN, PID: 24184988
    • Bergmann R, Ruffani A, Graham B et al (2013) Synthesis and radiopharmacological evaluation of (6)(4)Cu-labeled bombesin analogs featuring a bis(2-pyridylmethyl)-1,4,7-triazacyclononane chelator. Eur J Med Chem 70:434–446
    • (2013) Eur J Med Chem , vol.70 , pp. 434-446
    • Bergmann, R.1    Ruffani, A.2    Graham, B.3
  • 11
    • 69349102846 scopus 로고    scopus 로고
    • Evaluation of a 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid-conjugated bombesin-based radioantagonist for the labeling with single-photon emission computed tomography, positron emission tomography, and therapeutic radionuclides
    • COI: 1:CAS:528:DC%2BD1MXpvFeit7g%3D, PID: 19671861
    • Mansi R, Wang X, Forrer F et al (2009) Evaluation of a 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid-conjugated bombesin-based radioantagonist for the labeling with single-photon emission computed tomography, positron emission tomography, and therapeutic radionuclides. Clin Cancer Res 15:5240–5249
    • (2009) Clin Cancer Res , vol.15 , pp. 5240-5249
    • Mansi, R.1    Wang, X.2    Forrer, F.3
  • 12
    • 84862819921 scopus 로고    scopus 로고
    • Bombesin analogues for gastrin-releasing peptide receptor imaging
    • COI: 1:CAS:528:DC%2BC38XmtFantro%3D, PID: 22261143
    • Nanda PK, Pandey U, Bottenus BN et al (2012) Bombesin analogues for gastrin-releasing peptide receptor imaging. Nucl Med Biol 39:461–471
    • (2012) Nucl Med Biol , vol.39 , pp. 461-471
    • Nanda, P.K.1    Pandey, U.2    Bottenus, B.N.3
  • 13
    • 0038579396 scopus 로고    scopus 로고
    • [99mTc]Demobesin 1, a novel potent bombesin analogue for GRP receptor-targeted tumour imaging
    • COI: 1:CAS:528:DC%2BD3sXms1CntA%3D%3D, PID: 12552343
    • Nock B, Nikolopoulou A, Chiotellis E et al (2003) [99mTc]Demobesin 1, a novel potent bombesin analogue for GRP receptor-targeted tumour imaging. Eur J Nucl Med Mol Imaging 30:247–258
    • (2003) Eur J Nucl Med Mol Imaging , vol.30 , pp. 247-258
    • Nock, B.1    Nikolopoulou, A.2    Chiotellis, E.3
  • 14
    • 84901414418 scopus 로고    scopus 로고
    • A new (68)Ga-labeled BBN peptide with a hydrophilic linker for GRPR-targeted tumor imaging
    • COI: 1:CAS:528:DC%2BC2cXktlWltbc%3D, PID: 24633452
    • Pan D, Xu YP, Yang RH et al (2014) A new (68)Ga-labeled BBN peptide with a hydrophilic linker for GRPR-targeted tumor imaging. Amino Acids 46:1481–1489
    • (2014) Amino Acids , vol.46 , pp. 1481-1489
    • Pan, D.1    Xu, Y.P.2    Yang, R.H.3
  • 15
    • 84908009583 scopus 로고    scopus 로고
    • PET imaging of prostate tumors with 18F-Al-NOTA-MATBBN
    • COI: 1:CAS:528:DC%2BC2cXhslemt7bM, PID: 24729577
    • Pan D, Yan Y, Yang R et al (2014) PET imaging of prostate tumors with 18F-Al-NOTA-MATBBN. Contrast Media Mol Imaging 9:342–348
    • (2014) Contrast Media Mol Imaging , vol.9 , pp. 342-348
    • Pan, D.1    Yan, Y.2    Yang, R.3
  • 16
    • 84886295631 scopus 로고    scopus 로고
    • Synthesis and radiopharmacological evaluation of a high-affinity and metabolically stabilized 18F-labeled bombesin analogue for molecular imaging of gastrin-releasing peptide receptor-expressing prostate cancer
    • COI: 1:CAS:528:DC%2BC3sXht12is7bJ, PID: 23969085
    • Richter S, Wuest M, Krieger SS et al (2013) Synthesis and radiopharmacological evaluation of a high-affinity and metabolically stabilized 18F-labeled bombesin analogue for molecular imaging of gastrin-releasing peptide receptor-expressing prostate cancer. Nucl Med Biol 40:1025–1034
    • (2013) Nucl Med Biol , vol.40 , pp. 1025-1034
    • Richter, S.1    Wuest, M.2    Krieger, S.S.3
  • 17
    • 84891695913 scopus 로고    scopus 로고
    • In vitro and in vivo evaluation of a (18)F-labeled high affinity NOTA conjugated bombesin antagonist as a PET ligand for GRPR-targeted tumor imaging
    • PID: 24312607
    • Varasteh Z, Aberg O, Velikyan I et al (2013) In vitro and in vivo evaluation of a (18)F-labeled high affinity NOTA conjugated bombesin antagonist as a PET ligand for GRPR-targeted tumor imaging. PLoS One 8:e81932
    • (2013) PLoS One , vol.8 , pp. e81932
    • Varasteh, Z.1    Aberg, O.2    Velikyan, I.3
  • 18
    • 80455124484 scopus 로고    scopus 로고
    • F-labeled GRPR agonists and antagonists: a comparative study in prostate cancer imaging
    • COI: 1:CAS:528:DC%2BC38Xislalt7s%3D, PID: 21544226
    • Yang M, Gao H, Zhou Y et al (2011) F-labeled GRPR agonists and antagonists: a comparative study in prostate cancer imaging. Theranostics 1:220–229
    • (2011) Theranostics , vol.1 , pp. 220-229
    • Yang, M.1    Gao, H.2    Zhou, Y.3
  • 19
    • 84866427436 scopus 로고    scopus 로고
    • Evolution of bombesin conjugates for targeted PET imaging of tumors
    • COI: 1:CAS:528:DC%2BC38XhsVSjur7N, PID: 23024746
    • Zhang H, Abiraj K, Thorek DL et al (2012) Evolution of bombesin conjugates for targeted PET imaging of tumors. PLoS One 7:e44046
    • (2012) PLoS One , vol.7 , pp. e44046
    • Zhang, H.1    Abiraj, K.2    Thorek, D.L.3
  • 20
    • 84928162601 scopus 로고    scopus 로고
    • Dosimetry and first clinical evaluation of the new 18F-radiolabeled bombesin analogue BAY 864367 in patients with prostate cancer
    • COI: 1:CAS:528:DC%2BC2MXkvV2gtLk%3D, PID: 25678494
    • Sah BR, Burger IA, Schibli R et al (2015) Dosimetry and first clinical evaluation of the new 18F-radiolabeled bombesin analogue BAY 864367 in patients with prostate cancer. J Nucl Med 56:372–378
    • (2015) J Nucl Med , vol.56 , pp. 372-378
    • Sah, B.R.1    Burger, I.A.2    Schibli, R.3
  • 21
    • 79958060431 scopus 로고    scopus 로고
    • Gastrin-releasing peptide receptor-based targeting using bombesin analogues is superior to metabolism-based targeting using choline for in vivo imaging of human prostate cancer xenografts
    • COI: 1:CAS:528:DC%2BC3MXmvVaisLw%3D, PID: 21431398
    • Schroeder RP, van Weerden WM, Krenning EP et al (2011) Gastrin-releasing peptide receptor-based targeting using bombesin analogues is superior to metabolism-based targeting using choline for in vivo imaging of human prostate cancer xenografts. Eur J Nucl Med Mol Imaging 38:1257–1266
    • (2011) Eur J Nucl Med Mol Imaging , vol.38 , pp. 1257-1266
    • Schroeder, R.P.1    van Weerden, W.M.2    Krenning, E.P.3
  • 22
    • 38949198118 scopus 로고    scopus 로고
    • Bombesin receptor antagonists may be preferable to agonists for tumor targeting
    • COI: 1:CAS:528:DC%2BD1cXivVOltb8%3D, PID: 18199616
    • Cescato R, Maina T, Nock B et al (2008) Bombesin receptor antagonists may be preferable to agonists for tumor targeting. J Nucl Med 49:318–326
    • (2008) J Nucl Med , vol.49 , pp. 318-326
    • Cescato, R.1    Maina, T.2    Nock, B.3
  • 23
    • 55249096687 scopus 로고    scopus 로고
    • Design, synthesis, and biological evaluation of an antagonist-bombesin analogue as targeting vector
    • COI: 1:CAS:528:DC%2BD1cXhtFChtrrE, PID: 18808168
    • Abd-Elgaliel WR, Gallazzi F, Garrison JC et al (2008) Design, synthesis, and biological evaluation of an antagonist-bombesin analogue as targeting vector. Bioconjug Chem 19:2040–2048
    • (2008) Bioconjug Chem , vol.19 , pp. 2040-2048
    • Abd-Elgaliel, W.R.1    Gallazzi, F.2    Garrison, J.C.3
  • 24
    • 0032587522 scopus 로고    scopus 로고
    • Automated synthesis of [11C]choline, a positron-emitting tracer for tumor imaging
    • COI: 1:CAS:528:DyaK1MXhtlymtr0%3D, PID: 10070713
    • Hara T, Yuasa M (1999) Automated synthesis of [11C]choline, a positron-emitting tracer for tumor imaging. Appl Radiat Isot 50:531–533
    • (1999) Appl Radiat Isot , vol.50 , pp. 531-533
    • Hara, T.1    Yuasa, M.2
  • 25
    • 4644261118 scopus 로고    scopus 로고
    • Synthesis and preclinical evaluation of the choline transport tracer deshydroxy-[18F]fluorocholine ([18F]dOC)
    • COI: 1:CAS:528:DC%2BD2cXotFClsr4%3D, PID: 15464386
    • Henriksen G, Herz M, Hauser A et al (2004) Synthesis and preclinical evaluation of the choline transport tracer deshydroxy-[18F]fluorocholine ([18F]dOC). Nucl Med Biol 31:851–858
    • (2004) Nucl Med Biol , vol.31 , pp. 851-858
    • Henriksen, G.1    Herz, M.2    Hauser, A.3
  • 26
    • 62449092307 scopus 로고    scopus 로고
    • Performance evaluation of the Inveon dedicated PET preclinical tomograph based on the NEMA NU-4 standards
    • PID: 19223424
    • Bao Q, Newport D, Chen M et al (2009) Performance evaluation of the Inveon dedicated PET preclinical tomograph based on the NEMA NU-4 standards. J Nucl Med 50:401–408
    • (2009) J Nucl Med , vol.50 , pp. 401-408
    • Bao, Q.1    Newport, D.2    Chen, M.3
  • 27
    • 77958193859 scopus 로고    scopus 로고
    • In vitro and in vivo characterization of novel 18F-labeled bombesin analogues for targeting GRPR-positive tumors
    • COI: 1:CAS:528:DC%2BC3cXhtFOru7bO, PID: 20857927
    • Mu L, Honer M, Becaud J et al (2010) In vitro and in vivo characterization of novel 18F-labeled bombesin analogues for targeting GRPR-positive tumors. Bioconjug Chem 21:1864–1871
    • (2010) Bioconjug Chem , vol.21 , pp. 1864-1871
    • Mu, L.1    Honer, M.2    Becaud, J.3
  • 28
    • 33645958934 scopus 로고    scopus 로고
    • 18F-labeled bombesin analogs for targeting GRP receptor-expressing prostate cancer
    • COI: 1:CAS:528:DC%2BD28Xlt1Kmsb4%3D, PID: 16513619
    • Zhang X, Cai W, Cao F et al (2006) 18F-labeled bombesin analogs for targeting GRP receptor-expressing prostate cancer. J Nucl Med 47:492–501
    • (2006) J Nucl Med , vol.47 , pp. 492-501
    • Zhang, X.1    Cai, W.2    Cao, F.3
  • 29
    • 84930364730 scopus 로고    scopus 로고
    • Preclinical evaluation of a tailor-made DOTA-conjugated PSMA inhibitor with optimized linker moiety for imaging and endoradiotherapy of prostate cancer
    • COI: 1:CAS:528:DC%2BC2MXhsVantL7F, PID: 25883127
    • Benesova M, Schafer M, Bauder-Wust U et al (2015) Preclinical evaluation of a tailor-made DOTA-conjugated PSMA inhibitor with optimized linker moiety for imaging and endoradiotherapy of prostate cancer. J Nucl Med 56:914–920
    • (2015) J Nucl Med , vol.56 , pp. 914-920
    • Benesova, M.1    Schafer, M.2    Bauder-Wust, U.3
  • 30
    • 84890794697 scopus 로고    scopus 로고
    • Preclinical evaluation of BAY 1075553, a novel (18)F-labelled inhibitor of prostate-specific membrane antigen for PET imaging of prostate cancer
    • COI: 1:CAS:528:DC%2BC3sXhtlShtrvI, PID: 23955632
    • Lesche R, Kettschau G, Gromov AV et al (2014) Preclinical evaluation of BAY 1075553, a novel (18)F-labelled inhibitor of prostate-specific membrane antigen for PET imaging of prostate cancer. Eur J Nucl Med Mol Imaging 41:89–101
    • (2014) Eur J Nucl Med Mol Imaging , vol.41 , pp. 89-101
    • Lesche, R.1    Kettschau, G.2    Gromov, A.V.3
  • 31
    • 84938833007 scopus 로고    scopus 로고
    • 68Ga- and 177Lu-labeled PSMA I&T: optimization of a PSMA targeted theranostic concept and first proof of concept human studies
    • COI: 1:CAS:528:DC%2BC2MXitVSjt7zP, PID: 26089548
    • Weineisen M, Schottelius M, Simecek J et al (2015) 68Ga- and 177Lu-labeled PSMA I&T: optimization of a PSMA targeted theranostic concept and first proof of concept human studies. J Nucl Med 56:1169–1176
    • (2015) J Nucl Med , vol.56 , pp. 1169-1176
    • Weineisen, M.1    Schottelius, M.2    Simecek, J.3
  • 32
    • 84914695684 scopus 로고    scopus 로고
    • Synthesis and preclinical evaluation of DOTAGA-conjugated PSMA ligands for functional imaging and endoradiotherapy of prostate cancer
    • PID: 26116124
    • Weineisen M, Simecek J, Schottelius M et al (2014) Synthesis and preclinical evaluation of DOTAGA-conjugated PSMA ligands for functional imaging and endoradiotherapy of prostate cancer. EJNMMI Res 4:63
    • (2014) EJNMMI Res , vol.4 , pp. 63
    • Weineisen, M.1    Simecek, J.2    Schottelius, M.3


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