메뉴 건너뛰기




Volumn 32, Issue 5, 2014, Pages 795-805

Pharmacology, immunogenicity, and efficacy of a novel pegylated recombinant Erwinia chrysanthemi-derived L-asparaginase

Author keywords

Acute lymphoblastic leukemia; Erwinia chrysanthemi; L asparaginase; Lymphoma; Pegylation

Indexed keywords

ANTIBODY; ANTINEOPLASTIC AGENT; ASPARAGINASE; MACROGOL DERIVATIVE; RECOMBINANT PROTEIN;

EID: 84930732833     PISSN: 01676997     EISSN: 15730646     Source Type: Journal    
DOI: 10.1007/s10637-014-0102-9     Document Type: Article
Times cited : (29)

References (49)
  • 2
    • 0032613231 scopus 로고    scopus 로고
    • The three asparaginases. Comparative pharmacology and optimal use in childhood leukemia
    • Asselin BL (1999) The three asparaginases. Comparative pharmacology and optimal use in childhood leukemia. Adv Exp Med Biol 457:621-629
    • (1999) Adv Exp Med Biol , vol.457 , pp. 621-629
    • Asselin, B.L.1
  • 3
    • 84857497300 scopus 로고    scopus 로고
    • The right dose for the right patient
    • Asselin BL (2012) The right dose for the right patient. Blood 119(7):1617-1618
    • (2012) Blood , vol.119 , Issue.7 , pp. 1617-1618
    • Asselin, B.L.1
  • 4
    • 80455158087 scopus 로고    scopus 로고
    • Asparaginases: A successful class of drugs against leukemias and lymphomas
    • Avramis VI (2011) Asparaginases: a successful class of drugs against leukemias and lymphomas. J Pediatr Hematol Oncol 33(8):573-579
    • (2011) J Pediatr Hematol Oncol , vol.33 , Issue.8 , pp. 573-579
    • Avramis, V.I.1
  • 5
    • 84965111634 scopus 로고
    • Regression of transplanted lymphomas induced in vivo by means of normal guinea pig serum. I. Course of transplanted cancers of various kinds in mice and rats given guinea pig serum, horse serum, or rabbit serum
    • Kidd JG (1953) Regression of transplanted lymphomas induced in vivo by means of normal guinea pig serum. I. Course of transplanted cancers of various kinds in mice and rats given guinea pig serum, horse serum, or rabbit serum. J Exp Med 98(6):565-582
    • (1953) J Exp Med , vol.98 , Issue.6 , pp. 565-582
    • Kidd, J.G.1
  • 6
    • 75449125982 scopus 로고
    • Evidence that the L-asparaginase of guinea pig serum is responsible for its antilymphoma effects. II. Lymphoma 6C3HED cells cultured in a medium devoid of L-asparagine lose their susceptibility to the effects of guinea pig serum in vivo
    • Broome JD (1963) Evidence that the L-asparaginase of guinea pig serum is responsible for its antilymphoma effects. II. Lymphoma 6C3HED cells cultured in a medium devoid of L-asparagine lose their susceptibility to the effects of guinea pig serum in vivo. J Exp Med 118:121-148
    • (1963) J Exp Med , vol.118 , pp. 121-148
    • Broome, J.D.1
  • 7
    • 50549191387 scopus 로고
    • Tumor inhibitory effect of L-asparaginase fromescherichia coli
    • Mashburn LT, Wriston JC Jr (1964) Tumor inhibitory effect of L-asparaginase fromescherichia coli. Arch Biochem Biophys 105:450-452
    • (1964) Arch Biochem Biophys , vol.105 , pp. 450-452
    • Mashburn, L.T.1    Wriston, J.C.2
  • 10
    • 0018704340 scopus 로고
    • Effective dose of L-asparaginase for induction of remission in previously treated children with acute lymphocytic leukemia: A report from Childrens Cancer Study Group
    • Ertel IJ, Nesbit ME, Hammond D, Weiner J, Sather H (1979) Effective dose of L-asparaginase for induction of remission in previously treated children with acute lymphocytic leukemia: a report from Childrens Cancer Study Group. Cancer Res 39(10):3893-3896
    • (1979) Cancer Res , vol.39 , Issue.10 , pp. 3893-3896
    • Ertel, I.J.1    Nesbit, M.E.2    Hammond, D.3    Weiner, J.4    Sather, H.5
  • 11
    • 0014588094 scopus 로고
    • l-asparaginase resistance in human leukemia-asparagine synthetase
    • Haskell CM, Canellos GP (1969) l-asparaginase resistance in human leukemia-asparagine synthetase. Biochem Pharmacol 18(10):2578-2580
    • (1969) Biochem Pharmacol , vol.18 , Issue.10 , pp. 2578-2580
    • Haskell, C.M.1    Canellos, G.P.2
  • 12
    • 0030966193 scopus 로고    scopus 로고
    • Amino acid control of asparagine synthetase: Relation to asparaginase resistance in human leukemia cells
    • Hutson RG, Kitoh T, Moraga Amador DA, Cosic S, Schuster SM, Kilberg MS (1997) Amino acid control of asparagine synthetase: relation to asparaginase resistance in human leukemia cells. Am J Physiol 272(5 Pt 1):C1691-C1699
    • (1997) Am J Physiol , vol.272 , Issue.5 , pp. C1691-C1699
    • Hutson, R.G.1    Kitoh, T.2    Moraga Amador, D.A.3    Cosic, S.4    Schuster, S.M.5    Kilberg, M.S.6
  • 13
    • 0035397709 scopus 로고    scopus 로고
    • Asparagine synthetase expression alone is sufficient to induce l-asparaginase resistance in MOLT-4 human leukaemia cells
    • Aslanian AM, Fletcher BS, Kilberg MS (2001) Asparagine synthetase expression alone is sufficient to induce l-asparaginase resistance in MOLT-4 human leukaemia cells. Biochem J 357(Pt 1):321-328
    • (2001) Biochem J , vol.357 , pp. 321-328
    • Aslanian, A.M.1    Fletcher, B.S.2    Kilberg, M.S.3
  • 14
  • 15
    • 0042890525 scopus 로고    scopus 로고
    • L-asparaginase-based regimen in the treatment of refractory midline nasal/nasal-type T/NK-cell lymphoma
    • Yong W, Zheng W, Zhang Y, Zhu J, Wei Y, Zhu D, Li J (2003) L-asparaginase-based regimen in the treatment of refractory midline nasal/nasal-type T/NK-cell lymphoma. Int J Hematol 78(2):163-167
    • (2003) Int J Hematol , vol.78 , Issue.2 , pp. 163-167
    • Yong, W.1    Zheng, W.2    Zhang, Y.3    Zhu, J.4    Wei, Y.5    Zhu, D.6    Li, J.7
  • 16
    • 43649085643 scopus 로고    scopus 로고
    • Phase I study of dexamethasone, methotrexate, ifosfamide, L-asparaginase, and etoposide (SMILE) chemotherapy for advanced-stage, relapsed or refractory extranodal natural killer (NK)/T-cell lymphoma and leukemia
    • Yamaguchi M, Suzuki R, Kwong YL, Kim WS, Hasegawa Y, Izutsu K, Suzumiya J, Okamura T, Nakamura S, Kawa K, Oshimi K (2008) Phase I study of dexamethasone, methotrexate, ifosfamide, L-asparaginase, and etoposide (SMILE) chemotherapy for advanced-stage, relapsed or refractory extranodal natural killer (NK)/T-cell lymphoma and leukemia. Cancer Sci 99(5):1016-1020. doi:10.1111/j.1349-7006.2008.00768.x
    • (2008) Cancer Sci , vol.99 , Issue.5 , pp. 1016-1020
    • Yamaguchi, M.1    Suzuki, R.2    Kwong, Y.L.3    Kim, W.S.4    Hasegawa, Y.5    Izutsu, K.6    Suzumiya, J.7    Okamura, T.8    Nakamura, S.9    Kawa, K.10    Oshimi, K.11
  • 18
    • 0043261498 scopus 로고    scopus 로고
    • Pegylation: Engineering improved biopharmaceuticals for oncology
    • Molineux G (2003) Pegylation: engineering improved biopharmaceuticals for oncology. Pharmacotherapy 23(8 Pt 2):3S-8S
    • (2003) Pharmacotherapy , vol.23 , Issue.8 , pp. 3S-8S
    • Molineux, G.1
  • 20
    • 0041520550 scopus 로고    scopus 로고
    • Evaluation of immunologic crossreaction of antiasparaginase antibodies in acute lymphoblastic leukemia (ALL) and lymphoma patients
    • Wang B, Relling MV, Storm MC, Woo MH, Ribeiro R, Pui CH, Hak LJ (2003) Evaluation of immunologic crossreaction of antiasparaginase antibodies in acute lymphoblastic leukemia (ALL) and lymphoma patients. Leukemia 17(8):1583-1588
    • (2003) Leukemia , vol.17 , Issue.8 , pp. 1583-1588
    • Wang, B.1    Relling, M.V.2    Storm, M.C.3    Woo, M.H.4    Ribeiro, R.5    Pui, C.H.6    Hak, L.J.7
  • 25
    • 79551643513 scopus 로고    scopus 로고
    • Asparaginase revisited
    • van den Berg H (2011) Asparaginase revisited. Leuk Lymphoma 52(2):168-178. doi:10.3109/10428194.2010.537796
    • (2011) Leuk Lymphoma , vol.52 , Issue.2 , pp. 168-178
    • Van Den Berg, H.1
  • 27
    • 0015499931 scopus 로고
    • Isolation, crystallization, and properties of Achromobacteraceae glutaminase-asparaginase with antitumor activity
    • Roberts J, Holcenberg JS, Dolowy WC (1972) Isolation, crystallization, and properties of Achromobacteraceae glutaminase-asparaginase with antitumor activity. J Biol Chem 247(1):84-90
    • (1972) J Biol Chem , vol.247 , Issue.1 , pp. 84-90
    • Roberts, J.1    Holcenberg, J.S.2    Dolowy, W.C.3
  • 28
    • 0026757278 scopus 로고
    • Site-specific mutagenesis of Escherichia coli asparaginase II. None of the three histidine residues is required for catalysis
    • Wehner A, Harms E, Jennings MP, Beacham IR, Derst C, Bast P, Rohm KH (1992) Site-specific mutagenesis of Escherichia coli asparaginase II. None of the three histidine residues is required for catalysis. Eur J Biochem/FEBS 208(2):475-480
    • (1992) Eur J Biochem/FEBS , vol.208 , Issue.2 , pp. 475-480
    • Wehner, A.1    Harms, E.2    Jennings, M.P.3    Beacham, I.R.4    Derst, C.5    Bast, P.6    Rohm, K.H.7
  • 30
    • 0014573891 scopus 로고
    • Glutaminase activity of L-asparagine amidohydrolase
    • Miller HK, Balis ME (1969) Glutaminase activity of L-asparagine amidohydrolase. Biochem Pharmacol 18(9):2225-2232
    • (1969) Biochem Pharmacol , vol.18 , Issue.9 , pp. 2225-2232
    • Miller, H.K.1    Balis, M.E.2
  • 31
    • 18644364984 scopus 로고    scopus 로고
    • Pharmacokinetic/pharmacodynamic relationships of asparaginase formulations: The past, the present and recommendations for the future
    • Avramis VI, Panosyan EH (2005) Pharmacokinetic/pharmacodynamic relationships of asparaginase formulations: the past, the present and recommendations for the future. Clin Pharmacokinet 44(4):367-393
    • (2005) Clin Pharmacokinet , vol.44 , Issue.4 , pp. 367-393
    • Avramis, V.I.1    Panosyan, E.H.2
  • 33
    • 55749111387 scopus 로고    scopus 로고
    • The pharmacology of PEGylation: Balancing PD with PK to generate novel therapeutics
    • Fishburn CS (2007) The pharmacology of PEGylation: balancing PD with PK to generate novel therapeutics. J Pharm Sci 97(10):4167-4183
    • (2007) J Pharm Sci , vol.97 , Issue.10 , pp. 4167-4183
    • Fishburn, C.S.1
  • 34
    • 0037177490 scopus 로고    scopus 로고
    • Effects of polyethylene glycol attachment on physicochemical and biological stability of E. coli L-asparaginase
    • Soares AL, Guimaraes GM, Polakiewicz B, de Moraes Pitombo RN, Abrahao-Neto J (2002) Effects of polyethylene glycol attachment on physicochemical and biological stability of E. coli L-asparaginase. Int J Pharm 237(1-2):163-170
    • (2002) Int J Pharm , vol.237 , Issue.1-2 , pp. 163-170
    • Soares, A.L.1    Guimaraes, G.M.2    Polakiewicz, B.3    De Moraes Pitombo, R.N.4    Abrahao-Neto, J.5
  • 35
    • 11244314360 scopus 로고    scopus 로고
    • A genome-wide view of the in vitro response to l-asparaginase in acute lymphoblastic leukemia
    • Fine BM, Kaspers GJ, Ho M, Loonen AH, Boxer LM (2005) A genome-wide view of the in vitro response to l-asparaginase in acute lymphoblastic leukemia. Cancer Res 65(1):291-299
    • (2005) Cancer Res , vol.65 , Issue.1 , pp. 291-299
    • Fine, B.M.1    Kaspers, G.J.2    Ho, M.3    Loonen, A.H.4    Boxer, L.M.5
  • 38
    • 0023789865 scopus 로고
    • Asparaginase-induced derangements of glutamine metabolism: The pathogenetic basis for some drug-related side-effects
    • Ollenschlager G, Roth E, Linkesch W, Jansen S, Simmel A, Modder B (1988) Asparaginase-induced derangements of glutamine metabolism: the pathogenetic basis for some drug-related side-effects. Eur J Clin Invest 18(5):512-516
    • (1988) Eur J Clin Invest , vol.18 , Issue.5 , pp. 512-516
    • Ollenschlager, G.1    Roth, E.2    Linkesch, W.3    Jansen, S.4    Simmel, A.5    Modder, B.6
  • 39
    • 0020538536 scopus 로고
    • Kinetic analysis of hepatotoxicity associated with antineoplastic asparaginases
    • Durden DL, Salazar AM, Distasio JA (1983) Kinetic analysis of hepatotoxicity associated with antineoplastic asparaginases. Cancer Res 43(4):1602-1605
    • (1983) Cancer Res , vol.43 , Issue.4 , pp. 1602-1605
    • Durden, D.L.1    Salazar, A.M.2    Distasio, J.A.3
  • 40
    • 0018870253 scopus 로고
    • Comparison of the immunosuppressive effects of asparaginases from Escherichia coli and Vibrio succinogenes
    • Durden DL, Distasio JA (1980) Comparison of the immunosuppressive effects of asparaginases from Escherichia coli and Vibrio succinogenes. Cancer Res 40(4):1125-1129
    • (1980) Cancer Res , vol.40 , Issue.4 , pp. 1125-1129
    • Durden, D.L.1    Distasio, J.A.2
  • 41
    • 0014919874 scopus 로고
    • Dysmetabolic and neurological complications in leukemia patients treated with L-asparaginase
    • Storti E, Quaglino D (1970) Dysmetabolic and neurological complications in leukemia patients treated with L-asparaginase. Recent Results Cancer Res 33:344-349
    • (1970) Recent Results Cancer Res , vol.33 , pp. 344-349
    • Storti, E.1    Quaglino, D.2
  • 42
    • 0019952110 scopus 로고
    • Glutaminase-free asparaginase from vibrio succinogenes: An antilymphoma enzyme lacking hepatotoxicity
    • Distasio JA, Salazar AM, Nadji M, Durden DL (1982) Glutaminase-free asparaginase from vibrio succinogenes: an antilymphoma enzyme lacking hepatotoxicity. Int J Cancer 30(3):343-347
    • (1982) Int J Cancer , vol.30 , Issue.3 , pp. 343-347
    • Distasio, J.A.1    Salazar, A.M.2    Nadji, M.3    Durden, D.L.4
  • 43
    • 78650705940 scopus 로고    scopus 로고
    • Purification and characterization of glutaminase-free L-asparaginase from Pectobacterium carotovorum MTCC 1428
    • Kumar S, Venkata Dasu V, Pakshirajan K (2011) Purification and characterization of glutaminase-free L-asparaginase from Pectobacterium carotovorum MTCC 1428. Bioresour Technol 102(2):2077-2082. doi:10.1016/j.biortech.2010.07.114
    • (2011) Bioresour Technol , vol.102 , Issue.2 , pp. 2077-2082
    • Kumar, S.1    Venkata Dasu, V.2    Pakshirajan, K.3
  • 44
    • 0033773575 scopus 로고    scopus 로고
    • Engineering the substrate specificity of Escherichia coli asparaginase. II. Selective reduction of glutaminase activity by amino acid replacements at position 248
    • Derst C, Henseling J, Rohm KH (2000) Engineering the substrate specificity of Escherichia coli asparaginase. II. Selective reduction of glutaminase activity by amino acid replacements at position 248. Protein Sci Publ Protein Soc 9(10):2009-2017. doi:10.1110/ps.9.10.2009
    • (2000) Protein Sci Publ Protein Soc , vol.9 , Issue.10 , pp. 2009-2017
    • Derst, C.1    Henseling, J.2    Rohm, K.H.3
  • 45
    • 79551625096 scopus 로고    scopus 로고
    • Rational engineering of L-asparaginase reveals importance of dual activity for cancer cell toxicity
    • Offman MN, Krol M, Patel N, Krishnan S, Liu J, Saha V, Bates PA (2011) Rational engineering of L-asparaginase reveals importance of dual activity for cancer cell toxicity. Blood 117(5):1614-1621. doi:10.1182/blood-2010-07-298422
    • (2011) Blood , vol.117 , Issue.5 , pp. 1614-1621
    • Offman, M.N.1    Krol, M.2    Patel, N.3    Krishnan, S.4    Liu, J.5    Saha, V.6    Bates, P.A.7
  • 46
    • 0015979582 scopus 로고
    • Therapeutic properties of a new glutaminase-asparaginase preparation and the influence of the lactate dehydrogenase-elevating virus
    • Riley V, Spackman D, Fitzmaurice MA, Roberts J, Holcenberg JS, Dolowy WC (1974) Therapeutic properties of a new glutaminase-asparaginase preparation and the influence of the lactate dehydrogenase-elevating virus. Cancer Res 34(2):429-438
    • (1974) Cancer Res , vol.34 , Issue.2 , pp. 429-438
    • Riley, V.1    Spackman, D.2    Fitzmaurice, M.A.3    Roberts, J.4    Holcenberg, J.S.5    Dolowy, W.C.6
  • 49
    • 0029823598 scopus 로고    scopus 로고
    • Cell susceptibility to apoptosis by glutamine deprivation and rescue: Survival and apoptotic death in cultured lymphoma-leukemia cell lines
    • Petronini PG, Urbani S, Alfieri R, Borghetti AF, Guidotti GG (1996) Cell susceptibility to apoptosis by glutamine deprivation and rescue: survival and apoptotic death in cultured lymphoma-leukemia cell lines. J Cell Physiol 169(1):175-185. doi:10.1002/(SICI)1097-4652(199610)169:1〈175::AIDJCP18〉3.0.CO;2-C
    • (1996) J Cell Physiol , vol.169 , Issue.1 , pp. 175-185
    • Petronini, P.G.1    Urbani, S.2    Alfieri, R.3    Borghetti, A.F.4    Guidotti, G.G.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.