메뉴 건너뛰기




Volumn 72, Issue 6, 2013, Pages 1343-1352

A phase 1 trial of intravenous 4-(N-(S-glutathionylacetyl)amino) phenylarsenoxide (GSAO) in patients with advanced solid tumours

(28)  Horsley, Laura a,h   Cummings, Jeff b   Middleton, Mark c   Ward, Tim b   Backen, Alison b   Clamp, Andrew a,h   Dawson, Martin b   Farmer, Hayley d   Fisher, Nita e   Halbert, Gavin f   Halford, Sarah d   Harris, Adrian c   Hasan, Jurjees a,h   Hogg, Philip g   Kumaran, Gireesh a,h   Little, Ross h   Parker, Geoff J M h   Potter, Paula a   Saunders, Mark a,h   Roberts, Caleb h   more..


Author keywords

Clinical trial; DCE MRI; GSAO; Novel arsenic compound; Phase 1

Indexed keywords

4 [N (S GLUTATHIONYLACETYL)AMINO]PHENYLARSENOXIDE; ARSENOSOBENZENE; UNCLASSIFIED DRUG;

EID: 84890442259     PISSN: 03445704     EISSN: 14320843     Source Type: Journal    
DOI: 10.1007/s00280-013-2320-9     Document Type: Article
Times cited : (34)

References (25)
  • 1
    • 77952242853 scopus 로고    scopus 로고
    • Issues on fit-for-purpose validation of a panel of ELISAs for application as biomarkers in clinical trials of anti-Angiogenic drugs
    • 20407440 10.1038/sj.bjc.6605661 1:CAS:528:DC%2BC3cXlvVOgsbo%3D
    • Brookes K, Cummings J, Backen A, Greystoke A, Ward T, Jayson GC, Dive C (2010) Issues on fit-for-purpose validation of a panel of ELISAs for application as biomarkers in clinical trials of anti-Angiogenic drugs. Br J Cancer 102:1524-1532
    • (2010) Br J Cancer , vol.102 , pp. 1524-1532
    • Brookes, K.1    Cummings, J.2    Backen, A.3    Greystoke, A.4    Ward, T.5    Jayson, G.C.6    Dive, C.7
  • 2
    • 0029874761 scopus 로고    scopus 로고
    • Pharmacokinetics, metabolism and tumour disposition of 8-chloroadenosine 3′,5′-monophosphate in breast cancer patients and xenograft bearing mice
    • 8740794 10.1093/oxfordjournals.annonc.a010574 1:STN:280: DyaK28zivVGmsQ%3D%3D
    • Cummings J, Langdon SP, Ritchie AA, Burns DJ, Mackay J, Stockman P, Leonard RC, Miller WR (1996) Pharmacokinetics, metabolism and tumour disposition of 8-chloroadenosine 3′,5′-monophosphate in breast cancer patients and xenograft bearing mice. Ann Oncol 7:291-296
    • (1996) Ann Oncol , vol.7 , pp. 291-296
    • Cummings, J.1    Langdon, S.P.2    Ritchie, A.A.3    Burns, D.J.4    Mackay, J.5    Stockman, P.6    Leonard, R.C.7    Miller, W.R.8
  • 3
    • 33745529219 scopus 로고    scopus 로고
    • Method validation and preliminary qualification of pharmacodynamic biomarkers employed to evaluate the clinical efficacy of an antisense compound (AEG35156) targeted to the X-linked inhibitor of apoptosis protein XIAP
    • 16804528 10.1038/sj.bjc.6603220 1:CAS:528:DC%2BD28XmtFyrtb4%3D
    • Cummings J, Ranson M, Lacasse E, Ganganagari JR, St-Jean M, Jayson G, Durkin J, Dive C (2006) Method validation and preliminary qualification of pharmacodynamic biomarkers employed to evaluate the clinical efficacy of an antisense compound (AEG35156) targeted to the X-linked inhibitor of apoptosis protein XIAP. Br J Cancer 95:42-48
    • (2006) Br J Cancer , vol.95 , pp. 42-48
    • Cummings, J.1    Ranson, M.2    Lacasse, E.3    Ganganagari, J.R.4    St-Jean, M.5    Jayson, G.6    Durkin, J.7    Dive, C.8
  • 4
    • 15244345318 scopus 로고    scopus 로고
    • Validation of pharmacodynamic assays to evaluate the clinical efficacy of an antisense compound (AEG 35156) targeted to the X-linked inhibitor of apoptosis protein XIAP
    • 15685240 1:CAS:528:DC%2BD2MXhtFWntrs%3D
    • Cummings J, Ward TH, Lacasse E, Lefebvre C, St-Jean M, Durkin J, Ranson M, Dive C (2005) Validation of pharmacodynamic assays to evaluate the clinical efficacy of an antisense compound (AEG 35156) targeted to the X-linked inhibitor of apoptosis protein XIAP. Br J Cancer 92:532-538
    • (2005) Br J Cancer , vol.92 , pp. 532-538
    • Cummings, J.1    Ward, T.H.2    Lacasse, E.3    Lefebvre, C.4    St-Jean, M.5    Durkin, J.6    Ranson, M.7    Dive, C.8
  • 5
    • 70350075458 scopus 로고    scopus 로고
    • Optimization of the antitumor efficacy of a synthetic mitochondrial toxin by increasing the residence time in the cytosol
    • 19788237 10.1021/jm9008339 1:CAS:528:DC%2BD1MXhtF2ltbnM
    • Dilda PJ, Decollogne S, Weerakoon L, Norris MD, Haber M, Allen JD, Hogg PJ (2009) Optimization of the antitumor efficacy of a synthetic mitochondrial toxin by increasing the residence time in the cytosol. J Med Chem 52:6209-6216
    • (2009) J Med Chem , vol.52 , pp. 6209-6216
    • Dilda, P.J.1    Decollogne, S.2    Weerakoon, L.3    Norris, M.D.4    Haber, M.5    Allen, J.D.6    Hogg, P.J.7
  • 6
    • 27144434430 scopus 로고    scopus 로고
    • Mechanism of selectivity of an angiogenesis inhibitor from screening a genome-wide set of Saccharomyces cerevisiae deletion strains
    • 16234568 10.1093/jnci/dji316 1:CAS:528:DC%2BD2MXhtFCjtb7P
    • Dilda PJ, Don AS, Tanabe KM, Higgins VJ, Allen JD, Dawes IW, Hogg PJ (2005) Mechanism of selectivity of an angiogenesis inhibitor from screening a genome-wide set of Saccharomyces cerevisiae deletion strains. J Natl Cancer Inst 97:1539-1547
    • (2005) J Natl Cancer Inst , vol.97 , pp. 1539-1547
    • Dilda, P.J.1    Don, A.S.2    Tanabe, K.M.3    Higgins, V.J.4    Allen, J.D.5    Dawes, I.W.6    Hogg, P.J.7
  • 7
    • 58149095551 scopus 로고    scopus 로고
    • Metabolism of the tumor angiogenesis inhibitor 4-(N-(S- Glutathionylacetyl)amino)phenylarsonous acid
    • 18723877 10.1074/jbc.M804470200 1:CAS:528:DC%2BD1cXhsVylsrrM
    • Dilda PJ, Ramsay EE, Corti A, Pompella A, Hogg PJ (2008) Metabolism of the tumor angiogenesis inhibitor 4-(N-(S-Glutathionylacetyl)amino)phenylarsonous acid. J Biol Chem 283:35428-35434
    • (2008) J Biol Chem , vol.283 , pp. 35428-35434
    • Dilda, P.J.1    Ramsay, E.E.2    Corti, A.3    Pompella, A.4    Hogg, P.J.5
  • 8
    • 0142010897 scopus 로고    scopus 로고
    • A peptide trivalent arsenical inhibits tumor angiogenesis by perturbing mitochondrial function in angiogenic endothelial cells
    • 12781367 10.1016/S1535-6108(03)00109-0 1:CAS:528:DC%2BD3sXktlyiu7o%3D
    • Don AS, Kisker O, Dilda P, Donoghue N, Zhao X, Decollogne S, Creighton B, Flynn E, Folkman J, Hogg PJ (2003) A peptide trivalent arsenical inhibits tumor angiogenesis by perturbing mitochondrial function in angiogenic endothelial cells. Cancer Cell 3:497-509
    • (2003) Cancer Cell , vol.3 , pp. 497-509
    • Don, A.S.1    Kisker, O.2    Dilda, P.3    Donoghue, N.4    Zhao, X.5    Decollogne, S.6    Creighton, B.7    Flynn, E.8    Folkman, J.9    Hogg, P.J.10
  • 11
    • 0030576517 scopus 로고    scopus 로고
    • Patterns and emerging mechanisms of the angiogenic switch during tumorigenesis
    • 8756718 10.1016/S0092-8674(00)80108-7 1:CAS:528:DyaK28XltVSks7s%3D
    • Hanahan D, Folkman J (1996) Patterns and emerging mechanisms of the angiogenic switch during tumorigenesis. Cell 86:353-364
    • (1996) Cell , vol.86 , pp. 353-364
    • Hanahan, D.1    Folkman, J.2
  • 12
    • 0037036578 scopus 로고    scopus 로고
    • Arsenic toxicity and potential mechanisms of action
    • 12076506 10.1016/S0378-4274(02)00084-X 1:CAS:528:DC%2BD38XksFKqsLs%3D
    • Hughes MF (2002) Arsenic toxicity and potential mechanisms of action. Toxicol Lett 133:1-16
    • (2002) Toxicol Lett , vol.133 , pp. 1-16
    • Hughes, M.F.1
  • 13
    • 12144290503 scopus 로고    scopus 로고
    • Differentiation between cell death modes using measurements of different soluble forms of extracellular cytokeratin 18
    • 14996736 10.1158/0008-5472.CAN-03-2455 1:CAS:528:DC%2BD2cXhsleku7w%3D
    • Kramer G, Erdal H, Mertens HJ, Nap M, Mauermann J, Steiner G, Marberger M, Biven K, Shoshan MC, Linder S (2004) Differentiation between cell death modes using measurements of different soluble forms of extracellular cytokeratin 18. Cancer Res 64:1751-1756
    • (2004) Cancer Res , vol.64 , pp. 1751-1756
    • Kramer, G.1    Erdal, H.2    Mertens, H.J.3    Nap, M.4    Mauermann, J.5    Steiner, G.6    Marberger, M.7    Biven, K.8    Shoshan, M.C.9    Linder, S.10
  • 16
    • 84858738899 scopus 로고    scopus 로고
    • The tumour metabolism inhibitors GSAO and PENAO react with cysteines 57 and 257 of mitochondrial adenine nucleotide translocase
    • 22448968 10.1186/1475-2867-12-11 1:CAS:528:DC%2BC38XnslyhsLs%3D
    • Park D, Chiu J, Perrone GG, Dilda PJ, Hogg PJ (2012) The tumour metabolism inhibitors GSAO and PENAO react with cysteines 57 and 257 of mitochondrial adenine nucleotide translocase. Cancer Cell Int 12:11
    • (2012) Cancer Cell Int , vol.12 , pp. 11
    • Park, D.1    Chiu, J.2    Perrone, G.G.3    Dilda, P.J.4    Hogg, P.J.5
  • 17
    • 77649187594 scopus 로고    scopus 로고
    • Mitochondria as targets in angiogenesis inhibition
    • 19995570 10.1016/j.mam.2009.12.005 1:CAS:528:DC%2BC3cXjtVSrsro%3D
    • Park D, Dilda PJ (2010) Mitochondria as targets in angiogenesis inhibition. Mol Aspects Med 31:113-131
    • (2010) Mol Aspects Med , vol.31 , pp. 113-131
    • Park, D.1    Dilda, P.J.2
  • 18
    • 84856227857 scopus 로고    scopus 로고
    • Mitochondrial metabolism inhibitors for cancer therapy
    • 21918915 10.1007/s11095-011-0584-5 1:CAS:528:DC%2BC3MXhtFKqsbrL
    • Ramsay EE, Hogg PJ, Dilda PJ (2011) Mitochondrial metabolism inhibitors for cancer therapy. Pharm Res 28:2731-2744
    • (2011) Pharm Res , vol.28 , pp. 2731-2744
    • Ramsay, E.E.1    Hogg, P.J.2    Dilda, P.J.3
  • 22
    • 0031404162 scopus 로고    scopus 로고
    • Modeling tracer kinetics in dynamic Gd-DTPA MR imaging
    • 9039598 10.1002/jmri.1880070113 1:STN:280:DyaK2s7ptFKmsA%3D%3D
    • Tofts PS (1997) Modeling tracer kinetics in dynamic Gd-DTPA MR imaging. J Magn Reson Imaging 7:91-101
    • (1997) J Magn Reson Imaging , vol.7 , pp. 91-101
    • Tofts, P.S.1
  • 24
    • 0035038845 scopus 로고    scopus 로고
    • History of the development of arsenic derivatives in cancer therapy
    • 11331434 10.1634/theoncologist.6-suppl-2-3 1:CAS:528:DC%2BD3MXktVShsbc%3D
    • Waxman S, Anderson KC (2001) History of the development of arsenic derivatives in cancer therapy. Oncologist 6(Suppl 2):3-10
    • (2001) Oncologist , vol.6 , Issue.SUPPL. 2 , pp. 3-10
    • Waxman, S.1    Anderson, K.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.