메뉴 건너뛰기




Volumn 16, Issue 5, 2003, Pages 548-552

Melanogenesis and melanoma

Author keywords

Chemotherapy; Genoprotection; Immunotherapy; Photoprotection; Tyrosinase

Indexed keywords

MELANIN; MONOPHENOL MONOOXYGENASE; QUINONE DERIVATIVE;

EID: 0041335218     PISSN: 08935785     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-0749.2003.00069.x     Document Type: Review
Times cited : (131)

References (50)
  • 2
    • 0023882897 scopus 로고
    • The validity and practicality of sun-reactive skin types I through VI
    • Fitzpatrick TB. The validity and practicality of sun-reactive skin types I through VI. Arch Dermatol 1988;124:869-871
    • (1988) Arch Dermatol , vol.124 , pp. 869-871
    • Fitzpatrick, T.B.1
  • 3
    • 0035818451 scopus 로고    scopus 로고
    • Ultrastructural organization of eumelanin from Sepia officianalis measured by atomic force microscopy
    • Clancy CM, Simon JD. Ultrastructural organization of eumelanin from Sepia officianalis measured by atomic force microscopy. Biochemistry 2001;40:13353-13360
    • (2001) Biochemistry , vol.40 , pp. 13353-13360
    • Clancy, C.M.1    Simon, J.D.2
  • 4
    • 0002713189 scopus 로고    scopus 로고
    • Extracutaneous melanocytes
    • Nordlund JJ, Boissy RE, Hearing VJ, King RA, Ortonne J-P. New York: OUP
    • Boissy RE. Extracutaneous melanocytes. In: Nordlund JJ, Boissy RE, Hearing VJ, King RA, Ortonne J-P. The Pigmentary System. New York: OUP; 1998. pp. 59-73
    • (1998) The Pigmentary System , pp. 59-73
    • Boissy, R.E.1
  • 5
    • 0018149710 scopus 로고
    • A theoretical note on the topological features of melanin transfer
    • Riley PA. A theoretical note on the topological features of melanin transfer. Brit J Dermatol 1978;99:107-110
    • (1978) Brit J Dermatol , vol.99 , pp. 107-110
    • Riley, P.A.1
  • 6
    • 0025916156 scopus 로고
    • Melanogenesis: A realistic target for antimelanoma therapy?
    • Riley PA. Melanogenesis: a realistic target for antimelanoma therapy? Eur J Cancer 1991;27:1172-1177
    • (1991) Eur J Cancer , vol.27 , pp. 1172-1177
    • Riley, P.A.1
  • 7
    • 0013608392 scopus 로고    scopus 로고
    • Epidermal melanin: Sun screen or waste disposal?
    • Riley PA. Epidermal melanin: sun screen or waste disposal? Biologist 1997;44:408-411
    • (1997) Biologist , vol.44 , pp. 408-411
    • Riley, P.A.1
  • 8
    • 0037841882 scopus 로고    scopus 로고
    • Tyrosinase autoactivation and the chemistry of ortho-quinone amines
    • Land EJ, Ramsden CA, Riley PA. Tyrosinase autoactivation and the chemistry of ortho-quinone amines. Acc Chem Res 2003;36:300-308
    • (2003) Acc Chem Res , vol.36 , pp. 300-308
    • Land, E.J.1    Ramsden, C.A.2    Riley, P.A.3
  • 9
    • 1342335876 scopus 로고
    • Dendritic cell populations of the epidermis
    • Jarrett A. London: Academic Press
    • Riley PA. Dendritic cell populations of the epidermis. In: Jarrett A. The Physiology and Pathophysiology of the Skin. London: Academic Press; 1975. pp. 1101-1130
    • (1975) The Physiology and Pathophysiology of the Skin , pp. 1101-1130
    • Riley, P.A.1
  • 10
    • 0031782481 scopus 로고    scopus 로고
    • Demographic characteristics, pigmentary and cutaneous risk factors for squamous cell carcinoma of the skin: A case-control study
    • English DR, Armstrong BK, Kricker A, Winter MG, Heenan PJ. Demographic characteristics, pigmentary and cutaneous risk factors for squamous cell carcinoma of the skin: a case-control study. Int J Cancer 1998;76:628-634
    • (1998) Int J Cancer , vol.76 , pp. 628-634
    • English, D.R.1    Armstrong, B.K.2    Kricker, A.3    Winter, M.G.4    Heenan, P.J.5
  • 11
    • 0033770358 scopus 로고    scopus 로고
    • Epidemiology of melanoma
    • Marks R. Epidemiology of melanoma. Clin Exp Dermatol 2000;25:459-463
    • (2000) Clin Exp Dermatol , vol.25 , pp. 459-463
    • Marks, R.1
  • 12
    • 0029094918 scopus 로고
    • Cutaneous melanoma in women. V. Characteristics of those who tan and those who burn when exposed to summer sun
    • Cress RD, Holly EA, Ahn DK. Cutaneous melanoma in women. V. Characteristics of those who tan and those who burn when exposed to summer sun. Epidemiology 1995;6:538-543
    • (1995) Epidemiology , vol.6 , pp. 538-543
    • Cress, R.D.1    Holly, E.A.2    Ahn, D.K.3
  • 16
    • 0000032673 scopus 로고
    • The cytotoxicity of melanin precursors
    • Hochstein P, Cohen G. The cytotoxicity of melanin precursors. Ann N Y Acad Sci 1963;100:876-881
    • (1963) Ann N Y Acad Sci , vol.100 , pp. 876-881
    • Hochstein, P.1    Cohen, G.2
  • 17
    • 0009778391 scopus 로고    scopus 로고
    • Mechanisms of control of the cytotoxicity of orthoquinone intermediates of melanogenesis
    • Creveling CR. Johnson City: FP Graham Publishing
    • Smit NPM, Pavel S, Riley PA. Mechanisms of control of the cytotoxicity of orthoquinone intermediates of melanogenesis. In: Creveling CR. Role of Catechol Quinone Species in Cellular Toxicity. Johnson City: FP Graham Publishing; 1999. pp. 191-245
    • (1999) Role of Catechol Quinone Species in Cellular Toxicity , pp. 191-245
    • Smit, N.P.M.1    Pavel, S.2    Riley, P.A.3
  • 18
    • 0028351403 scopus 로고
    • Role of gene expression and protein synthesis of tyrosinase, TRP-1, lamp-1, and CD63 in UVB-induced melanogenesis in human melanomas
    • Hara H, Lee MH, Chen H, Luo D, Jimbow K. Role of gene expression and protein synthesis of tyrosinase, TRP-1, lamp-1, and CD63 in UVB-induced melanogenesis in human melanomas. J Invest Dermatol 1994;102:495-500
    • (1994) J Invest Dermatol , vol.102 , pp. 495-500
    • Hara, H.1    Lee, M.H.2    Chen, H.3    Luo, D.4    Jimbow, K.5
  • 19
    • 0025886313 scopus 로고
    • Possible relationship between abnormal melanosome structure and cytotoxic phenomena in malignant melanoma
    • Borovansky J, Mirejovsky P, Riley PA. Possible relationship between abnormal melanosome structure and cytotoxic phenomena in malignant melanoma. Neoplasma 1991;38:393-400
    • (1991) Neoplasma , vol.38 , pp. 393-400
    • Borovansky, J.1    Mirejovsky, P.2    Riley, P.A.3
  • 20
    • 0027296389 scopus 로고
    • Properties of melanosomes and their exploitation in the diagnosis and treatment of melanoma
    • Borovansky J. Properties of melanosomes and their exploitation in the diagnosis and treatment of melanoma. Melanoma Res 1993;3:181-186
    • (1993) Melanoma Res , vol.3 , pp. 181-186
    • Borovansky, J.1
  • 23
    • 0018345507 scopus 로고
    • Selective toxicity of 6-hydroxydopa for melanoma cells
    • Wick MM, Byers L, Ratliff J. Selective toxicity of 6-hydroxydopa for melanoma cells. J Invest Dermatol 1979;72:67-69
    • (1979) J Invest Dermatol , vol.72 , pp. 67-69
    • Wick, M.M.1    Byers, L.2    Ratliff, J.3
  • 24
    • 0019944188 scopus 로고
    • Agents with potential specificity against melanotic melanoma
    • Lin AJ, Kelley JA, Breitman TR, Driscoll JS. Agents with potential specificity against melanotic melanoma. J Med Chem 1982;25:501-505
    • (1982) J Med Chem , vol.25 , pp. 501-505
    • Lin, A.J.1    Kelley, J.A.2    Breitman, T.R.3    Driscoll, J.S.4
  • 25
    • 0043193607 scopus 로고
    • In vitro studies of 2,4-dihydroxyphenylalanine, a prodrug targeted against malignant melanoma cells
    • Morrison ME, Yagi MJ, Cohen G. In vitro studies of 2,4-dihydroxyphenylalanine, a prodrug targeted against malignant melanoma cells. Proc Natl Acad Sci USA 1985;82:2960-2964
    • (1985) Proc Natl Acad Sci USA , vol.82 , pp. 2960-2964
    • Morrison, M.E.1    Yagi, M.J.2    Cohen, G.3
  • 27
    • 0023802961 scopus 로고
    • Structure-activity relationships defining the cytotoxicity of catechol analogues against human malignant melanoma
    • Kern DH, Shoemaker RH, Hildebrand-Zanki SU, Driscoll JS. Structure-activity relationships defining the cytotoxicity of catechol analogues against human malignant melanoma. Cancer Res 1988;48:5178-5182
    • (1988) Cancer Res , vol.48 , pp. 5178-5182
    • Kern, D.H.1    Shoemaker, R.H.2    Hildebrand-Zanki, S.U.3    Driscoll, J.S.4
  • 28
    • 0024486640 scopus 로고
    • Specificity of growth inhibition of melanoma by 4-hydroxyanisole
    • Kulkarni GA, Nathanson L. Specificity of growth inhibition of melanoma by 4-hydroxyanisole. Pigment Cell Res 1989;2:40-43
    • (1989) Pigment Cell Res , vol.2 , pp. 40-43
    • Kulkarni, G.A.1    Nathanson, L.2
  • 29
    • 0025339155 scopus 로고
    • Melanocytotoxicity and antimelanoma effects of phenolic amine compounds in mice in vivo
    • Alena F, Jimbow K, Ito S. Melanocytotoxicity and antimelanoma effects of phenolic amine compounds in mice in vivo. Cancer Res 1990;50:3743-3747
    • (1990) Cancer Res , vol.50 , pp. 3743-3747
    • Alena, F.1    Jimbow, K.2    Ito, S.3
  • 30
    • 0025223134 scopus 로고
    • The in vivo antimelanoma effect of 4-S-cysteaminylphenol and its n-acetyl derivative
    • Miura T, Jimbow K, Ito S. The in vivo antimelanoma effect of 4-S-cysteaminylphenol and its n-acetyl derivative. Int J Cancer 1990;46:931-934
    • (1990) Int J Cancer , vol.46 , pp. 931-934
    • Miura, T.1    Jimbow, K.2    Ito, S.3
  • 31
    • 0026167051 scopus 로고
    • Action of cysteaminylphenols on human melanoma cells in vivo and in vitro: 4-S-cysteaminylphenol binds protein disulphide isomerase
    • Parsons PG, Favier D, McEwan M, Takahashi H, Jimbow K, Ito S. Action of cysteaminylphenols on human melanoma cells in vivo and in vitro: 4-S-cysteaminylphenol binds protein disulphide isomerase. Melanoma Res 1991;1:97-104
    • (1991) Melanoma Res , vol.1 , pp. 97-104
    • Parsons, P.G.1    Favier, D.2    McEwan, M.3    Takahashi, H.4    Jimbow, K.5    Ito, S.6
  • 32
    • 0026717339 scopus 로고
    • Synthesis and cytotoxic properties of new N-substituted 4-aminophenol derivatives with a potential as antimelanoma agents
    • Mascagna D, Ghanem G, Morandini R, d'Ischia M, Misuraca G, Lejeune F, Prota G. Synthesis and cytotoxic properties of new N-substituted 4-aminophenol derivatives with a potential as antimelanoma agents. Melanoma Res 1992;2:25-32
    • (1992) Melanoma Res , vol.2 , pp. 25-32
    • Mascagna, D.1    Ghanem, G.2    Morandini, R.3    D'Ischia, M.4    Misuraca, G.5    Lejeune, F.6    Prota, G.7
  • 33
    • 0030737929 scopus 로고    scopus 로고
    • Dihydro-1,4-benzothiazine-6,7-dione, the ultimate toxic metabolite of 4-S-cysteaminylphenol and 4-S-cysteaminylcatechol
    • Hasegawa K, Ito S, Inoue S, Wakamatsu K, Ozeki H, Ishiguro I. Dihydro-1,4-benzothiazine-6,7-dione, the ultimate toxic metabolite of 4-S-cysteaminylphenol and 4-S-cysteaminylcatechol. Biochem Pharmacol 1997;53:1435-1444
    • (1997) Biochem Pharmacol , vol.53 , pp. 1435-1444
    • Hasegawa, K.1    Ito, S.2    Inoue, S.3    Wakamatsu, K.4    Ozeki, H.5    Ishiguro, I.6
  • 34
    • 0031897125 scopus 로고    scopus 로고
    • Comparison of antimelanoma effects of 4-S-cysteaminylphenol and its homologues
    • Inoue S, Hasegawa K, Wakamatsu K, Ito S. Comparison of antimelanoma effects of 4-S-cysteaminylphenol and its homologues. Melanoma Res 1998;8:105-112
    • (1998) Melanoma Res , vol.8 , pp. 105-112
    • Inoue, S.1    Hasegawa, K.2    Wakamatsu, K.3    Ito, S.4
  • 35
    • 0034050429 scopus 로고    scopus 로고
    • Comparison of in vitro cytotoxicity of N-acetyl and N-propionyl derivatives of phenolic thioether amines in melanoma and neuroblastoma cells and the relationship to tyrosinase and tyrosine hydroxylase enzyme activity
    • Gili A, Thomas PD, Ota M, Jimbow K. Comparison of in vitro cytotoxicity of N-acetyl and N-propionyl derivatives of phenolic thioether amines in melanoma and neuroblastoma cells and the relationship to tyrosinase and tyrosine hydroxylase enzyme activity. Melanoma Res 2000;10:9-15
    • (2000) Melanoma Res , vol.10 , pp. 9-15
    • Gili, A.1    Thomas, P.D.2    Ota, M.3    Jimbow, K.4
  • 36
    • 0035195981 scopus 로고    scopus 로고
    • Synthesis and anti-melanoma activity of analogues of N-acetyl-4-S-cysteaminylphenol substituted with two methyl groups alpha to the nitrogen
    • Lant NJ, McKeown P, Timoney MC, Kelland LR, Rogers PM, Robins DJ. Synthesis and anti-melanoma activity of analogues of N-acetyl-4-S-cysteaminylphenol substituted with two methyl groups alpha to the nitrogen. Anticancer Drug Des 2001;16:49-55
    • (2001) Anticancer Drug Des , vol.16 , pp. 49-55
    • Lant, N.J.1    McKeown, P.2    Timoney, M.C.3    Kelland, L.R.4    Rogers, P.M.5    Robins, D.J.6
  • 37
    • 0026251851 scopus 로고
    • In vitro assessment of the structure-activity relationship of tyrosinase-dependent cytotoxicity of a series of substituted phenols
    • Naish-Byfield S, Cooksey CJ, Latter AM, Johnson CI, Riley PA. In vitro assessment of the structure-activity relationship of tyrosinase-dependent cytotoxicity of a series of substituted phenols. Melanoma Res 1991;1:273-287
    • (1991) Melanoma Res , vol.1 , pp. 273-287
    • Naish-Byfield, S.1    Cooksey, C.J.2    Latter, A.M.3    Johnson, C.I.4    Riley, P.A.5
  • 38
    • 0027476649 scopus 로고
    • Reactivity of orthoquinones involved in tyrosinase-dependent cytotoxicity: Difference between alkylthio- and alkoxy-substituents
    • Cooksey CJ, Jimbow K, Land EJ, Riley PA. Reactivity of orthoquinones involved in tyrosinase-dependent cytotoxicity: difference between alkylthio- and alkoxy-substituents. Melanoma Res 1992;2:283-293
    • (1992) Melanoma Res , vol.2 , pp. 283-293
    • Cooksey, C.J.1    Jimbow, K.2    Land, E.J.3    Riley, P.A.4
  • 40
    • 0028956822 scopus 로고
    • Tyrosinase-mediated cytotoxicity of 4-substituted phenols: Quantitative structure-thiol reactivity relationships of the derived ortho-quinones
    • Cooksey CJ, Land EJ, Ramsden CA, Riley PA. Tyrosinase-mediated cytotoxicity of 4-substituted phenols: quantitative structure-thiol reactivity relationships of the derived ortho-quinones. Cancer Drug Design 1995;10:119-129
    • (1995) Cancer Drug Design , vol.10 , pp. 119-129
    • Cooksey, C.J.1    Land, E.J.2    Ramsden, C.A.3    Riley, P.A.4
  • 41
    • 0011461815 scopus 로고    scopus 로고
    • New approaches to the utilization of the melanogenic pathway in antimetanoma therapy
    • Hori Y, Hearing VJ, Nakayama J. Amsterdam: Elsevier
    • Riley PA. New approaches to the utilization of the melanogenic pathway in antimetanoma therapy. In: Hori Y, Hearing VJ, Nakayama J. Melanogenesis and Malignant Melanoma. Amsterdam: Elsevier; 1996. pp. 271-275
    • (1996) Melanogenesis and Malignant Melanoma , pp. 271-275
    • Riley, P.A.1
  • 42
    • 0030462560 scopus 로고    scopus 로고
    • Tyrosinase-mediated cytotoxicity of 4-substituted phenols: Use of QSAR to forecast reactivities of thiols towards the derived orthoquinones
    • Cooksey CJ, Land EJ, Rushton FAP, Ramsden CA, Riley PA. Tyrosinase-mediated cytotoxicity of 4-substituted phenols: use of QSAR to forecast reactivities of thiols towards the derived orthoquinones. Quant Struct - Act Relat 1996;15:498-503
    • (1996) Quant Struct - Act Relat , vol.15 , pp. 498-503
    • Cooksey, C.J.1    Land, E.J.2    Rushton, F.A.P.3    Ramsden, C.A.4    Riley, P.A.5
  • 43
    • 0031020020 scopus 로고    scopus 로고
    • Melanogenesis-targeted anti-melanoma pro-drug development: Effect of side-chain variations on the cytotoxicity of tyrosinase-generated orthoquinones in a model screening system
    • Riley PA, Cooksey CJ, Johnson CI, Land EJ, Latter AM, Ramsden CA. Melanogenesis-targeted anti-melanoma pro-drug development: effect of side-chain variations on the cytotoxicity of tyrosinase-generated orthoquinones in a model screening system. Eur J Canc 1997;33:135-143
    • (1997) Eur J Canc , vol.33 , pp. 135-143
    • Riley, P.A.1    Cooksey, C.J.2    Johnson, C.I.3    Land, E.J.4    Latter, A.M.5    Ramsden, C.A.6
  • 45
    • 0029348425 scopus 로고
    • New thioureas and related substances intended for melanoma targeting
    • Mars U, Larsson BS. New thioureas and related substances intended for melanoma targeting. Pigment Cell Res 1995;8:194-201
    • (1995) Pigment Cell Res , vol.8 , pp. 194-201
    • Mars, U.1    Larsson, B.S.2
  • 46
    • 0025221077 scopus 로고
    • Selective uptake of 2-thiouracil into melanin-producing systems depends on chemical binding to enzymically generated dopaquinone
    • Palumbo A, d'Ischia M, Misuraca G, Iannone A, Prota G. Selective uptake of 2-thiouracil into melanin-producing systems depends on chemical binding to enzymically generated dopaquinone. Biochim Biophys Acta 1990;1036:221-227
    • (1990) Biochim Biophys Acta , vol.1036 , pp. 221-227
    • Palumbo, A.1    D'Ischia, M.2    Misuraca, G.3    Iannone, A.4    Prota, G.5
  • 47
    • 0024695752 scopus 로고
    • Boron neutron capture therapy for malignant melanoma: An experimental approach
    • Larsson BS, Larsson B, Roberto A. Boron neutron capture therapy for malignant melanoma: an experimental approach. Pigment Cell Res 1989;2:356-360
    • (1989) Pigment Cell Res , vol.2 , pp. 356-360
    • Larsson, B.S.1    Larsson, B.2    Roberto, A.3
  • 49
    • 0032860282 scopus 로고    scopus 로고
    • Melanocyte-directed enzyme pro-drug therapy (MDEPT): Development of a targeted treatment for malignant melanoma
    • Jordan AM, Khan TH, Osborn HMI, Photiou A, Riley PA. Melanocyte-directed enzyme pro-drug therapy (MDEPT): development of a targeted treatment for malignant melanoma. Bioorg Med Chem 1999;7:1775-1780
    • (1999) Bioorg Med Chem , vol.7 , pp. 1775-1780
    • Jordan, A.M.1    Khan, T.H.2    Osborn, H.M.I.3    Photiou, A.4    Riley, P.A.5
  • 50
    • 0034936580 scopus 로고    scopus 로고
    • Melanocyte-directed enzyme pro-drug therapy (MDEPT): Development of second-generation prodrugs for targeted treatment of malignant melanoma
    • Jordan AM, Khan TH, Malkin H, Osborn HMI, Photiou A, Riley PA. Melanocyte-directed enzyme pro-drug therapy (MDEPT): development of second-generation prodrugs for targeted treatment of malignant melanoma. Bioorg Med Chem 2001;9:1549-1558
    • (2001) Bioorg Med Chem , vol.9 , pp. 1549-1558
    • Jordan, A.M.1    Khan, T.H.2    Malkin, H.3    Osborn, H.M.I.4    Photiou, A.5    Riley, P.A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.