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Volumn 21, Issue 6, 2008, Pages 700-709

CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma

Author keywords

CDKN2A; Familial melanoma; Germline mutations; MC1R; Multiple melanoma

Indexed keywords

CYCLIN DEPENDENT KINASE INHIBITOR 2A;

EID: 56249147495     PISSN: None     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1755-148X.2008.00512.x     Document Type: Article
Times cited : (46)

References (47)
  • 1
    • 0036895738 scopus 로고    scopus 로고
    • CDKN2A germline mutations in familial pancreatic cancer
    • Bartsch, D.K., Sina-Frey, M., Lang, S., et al. (2002). CDKN2A germline mutations in familial pancreatic cancer. Ann Surg. 236, 730 737.
    • (2002) Ann Surg. , vol.236 , pp. 730-737
    • Bartsch, D.K.1    Sina-Frey, M.2    Lang, S.3
  • 3
    • 33748056073 scopus 로고    scopus 로고
    • The prevalence of CDKN2A germ-line mutations and relative risk for cutaneous malignant melanoma: An international population-based study
    • Berwick, M., Orlow, I., Hummer, A.J. et al. (2006). The prevalence of CDKN2A germ-line mutations and relative risk for cutaneous malignant melanoma: an international population-based study. Cancer Epidemiol. Biomarkers Prev. 15, 1520 1555.
    • (2006) Cancer Epidemiol. Biomarkers Prev. , vol.15 , pp. 1520-1555
    • Berwick, M.1    Orlow, I.2    Hummer, A.J.3
  • 6
    • 0035860135 scopus 로고    scopus 로고
    • CDKN2A and CDK4 mutation analysis in Italian melanoma-prone families: Functional characterization of a novel CDKN2A germ line mutation
    • Della Torre, G., Pasini, B., Frigerio, S. et al. (2001). CDKN2A and CDK4 mutation analysis in Italian melanoma-prone families: functional characterization of a novel CDKN2A germ line mutation. Br. J. Cancer 85, 836 844.
    • (2001) Br. J. Cancer , vol.85 , pp. 836-844
    • Della Torre, G.1    Pasini, B.2    Frigerio, S.3
  • 7
    • 35448938787 scopus 로고    scopus 로고
    • Melanocytic nevi and sun exposure in a cohort of colorado children: Anatomic distribution and site-specific sunburn
    • Dodd, A.T., Morelli, J., Mokrohisky, S.T., Asdigian, N., Byers, T.E. Crane, L.A. (2007). Melanocytic nevi and sun exposure in a cohort of colorado children: anatomic distribution and site-specific sunburn. Cancer Epidemiol. Biomarkers Prev. 16, 2136 2143.
    • (2007) Cancer Epidemiol. Biomarkers Prev. , vol.16 , pp. 2136-2143
    • Dodd, A.T.1    Morelli, J.2    Mokrohisky, S.T.3    Asdigian, N.4    Byers, T.E.5    Crane, L.A.6
  • 12
    • 0032859717 scopus 로고    scopus 로고
    • Characterization of ligurian melanoma families and risk of occurrence of other neoplasia
    • Ghiorzo, P., Ciotti, P., Mantelli, M., et al. (1999). Characterization of ligurian melanoma families and risk of occurrence of other neoplasia. Int. J. Cancer. 83, 441 448.
    • (1999) Int. J. Cancer. , vol.83 , pp. 441-448
    • Ghiorzo, P.1    Ciotti, P.2    Mantelli, M.3
  • 13
    • 33748750438 scopus 로고    scopus 로고
    • Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma
    • Ghiorzo, P., Gargiulo, S., Pastorino, L. et al. (2006). Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma. Hum. Mol. Genet. 15, 2682 2689.
    • (2006) Hum. Mol. Genet. , vol.15 , pp. 2682-2689
    • Ghiorzo, P.1    Gargiulo, S.2    Pastorino, L.3
  • 15
    • 33750567811 scopus 로고    scopus 로고
    • High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL
    • Goldstein, A.M., Chan, M., Harland, M. et al. (2006). High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL. Cancer Res. 66, 9818 9828.
    • (2006) Cancer Res. , vol.66 , pp. 9818-9828
    • Goldstein, A.M.1    Chan, M.2    Harland, M.3
  • 16
    • 34547101440 scopus 로고    scopus 로고
    • Cutaneous phenotype and MC1R variants as modifying factors for the development of melanoma in CDKN2A G101W mutation carriers from 4 countries
    • Goldstein, A.M., Chaudru, V., Ghiorzo, P. et al. (2007). Cutaneous phenotype and MC1R variants as modifying factors for the development of melanoma in CDKN2A G101W mutation carriers from 4 countries. Int. J. Cancer 121, 825 831.
    • (2007) Int. J. Cancer , vol.121 , pp. 825-831
    • Goldstein, A.M.1    Chaudru, V.2    Ghiorzo, P.3
  • 17
    • 0034671754 scopus 로고    scopus 로고
    • CDKN2A germ-line mutations in individuals with multiple cutaneous melanomas
    • Hashemi, J., Platz, A., Ueno, T., Stierner, U., Ringborg, U. Hansson, J. (2000). CDKN2A germ-line mutations in individuals with multiple cutaneous melanomas. Cancer Res. 60, 6864 6867.
    • (2000) Cancer Res. , vol.60 , pp. 6864-6867
    • Hashemi, J.1    Platz, A.2    Ueno, T.3    Stierner, U.4    Ringborg, U.5    Hansson, J.6
  • 18
    • 38049021654 scopus 로고    scopus 로고
    • Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas
    • Helsing, P., Nymoen, D.A., Ariansen, S. et al. (2008). Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas. Genes Chromosomes Cancer 47, 175 184.
    • (2008) Genes Chromosomes Cancer , vol.47 , pp. 175-184
    • Helsing, P.1    Nymoen, D.A.2    Ariansen, S.3
  • 19
    • 0032784037 scopus 로고    scopus 로고
    • CDKN2A (P16(INK4a)) and CDK4 mutation analysis in 131 Australian melanoma probands: Effect of family history and multiple primary melanomas
    • Holland, E.A., Schmid, H., Kefford, R.F. Mann, G.J. (1999). CDKN2A (P16(INK4a)) and CDK4 mutation analysis in 131 Australian melanoma probands: effect of family history and multiple primary melanomas. Genes Chromosomes Cancer 25, 339 348.
    • (1999) Genes Chromosomes Cancer , vol.25 , pp. 339-348
    • Holland, E.A.1    Schmid, H.2    Kefford, R.F.3    Mann, G.J.4
  • 22
    • 0036550115 scopus 로고    scopus 로고
    • Four novel variants in MC1R in red-haired South African individuals of European descent: S83P, Y152X, A171D, P256S
    • John, P.R. Ramsay, M. (2002). Four novel variants in MC1R in red-haired South African individuals of European descent: S83P, Y152X, A171D, P256S. Hum. Mutat. 19, 461 462.
    • (2002) Hum. Mutat. , vol.19 , pp. 461-462
    • John, P.R.1    Ramsay, M.2
  • 24
    • 33749481705 scopus 로고    scopus 로고
    • Population-based study of natural variation in the melanocortin-1 receptor gene and melanoma
    • Kanetsky, P.A., Rebbeck, T.R., Hummer, A.J. et al. (2006). Population-based study of natural variation in the melanocortin-1 receptor gene and melanoma. Cancer Res. 66, 9330 9337.
    • (2006) Cancer Res. , vol.66 , pp. 9330-9337
    • Kanetsky, P.A.1    Rebbeck, T.R.2    Hummer, A.J.3
  • 25
    • 0032887878 scopus 로고    scopus 로고
    • Counseling and DNA testing for individuals perceived to be genetically predisposed to melanoma: A consensus statement of the Melanoma Genetics Consortium
    • Kefford, R.F., Newton Bishop, J.A., Bergman, W. Tucker, M.A. (1999). Counseling and DNA testing for individuals perceived to be genetically predisposed to melanoma: a consensus statement of the Melanoma Genetics Consortium. J. Clin. Oncol. 10, 3245 3251.
    • (1999) J. Clin. Oncol. , vol.10 , pp. 3245-3251
    • Kefford, R.F.1    Newton Bishop, J.A.2    Bergman, W.3    Tucker, M.A.4
  • 26
    • 0036143702 scopus 로고    scopus 로고
    • Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: The familial atypical mole melanoma-pancreatic carcinoma syndrome
    • Lynch, H.T., Brand, R.E., Hogg, D. et al. (2002). Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: the familial atypical mole melanoma-pancreatic carcinoma syndrome. Cancer 94, 84 96.
    • (2002) Cancer , vol.94 , pp. 84-96
    • Lynch, H.T.1    Brand, R.E.2    Hogg, D.3
  • 28
    • 18244408287 scopus 로고    scopus 로고
    • High prevalence of the G101W germline mutation in the CDKN2A (P16(ink4a)) gene in 62 Italian malignant melanoma families
    • Mantelli, M., Barile, M., Ciotti, P. et al. (2002). High prevalence of the G101W germline mutation in the CDKN2A (P16(ink4a)) gene in 62 Italian malignant melanoma families. Am. J. Med. Genet. 107, 214 221.
    • (2002) Am. J. Med. Genet. , vol.107 , pp. 214-221
    • Mantelli, M.1    Barile, M.2    Ciotti, P.3
  • 29
    • 13544259887 scopus 로고    scopus 로고
    • Early onset may predict G101W CDKN2A founder mutation carrier status in Ligurian melanoma patients
    • Mantelli, M., Pastorino, L., Ghiorzo, P. et al. (2004). Early onset may predict G101W CDKN2A founder mutation carrier status in Ligurian melanoma patients. Melanoma Res. 14, 443 448.
    • (2004) Melanoma Res. , vol.14 , pp. 443-448
    • Mantelli, M.1    Pastorino, L.2    Ghiorzo, P.3
  • 31
    • 56249137538 scopus 로고
    • release 16.0.1. Chicago: SPSS Inc.
    • Norusis, M.J. (1989-2007). SPSS 16.0, release 16.0.1. Chicago : SPSS Inc.
    • (1989) SPSS 16.0
    • Norusis, M.J.1
  • 33
    • 34249042388 scopus 로고    scopus 로고
    • CDKN2A and CDK4 variants in Latvian melanoma patients: Analysis of a clinic-based population
    • Pjanova, D., Engele, L., Randerson-Moor, J.A. et al. (2007). CDKN2A and CDK4 variants in Latvian melanoma patients: analysis of a clinic-based population. Melanoma Res. 17, 185 191.
    • (2007) Melanoma Res. , vol.17 , pp. 185-191
    • Pjanova, D.1    Engele, L.2    Randerson-Moor, J.A.3
  • 34
    • 0029147195 scopus 로고
    • Evidence for u.v. induction of CDKN2 mutations in melanoma cell lines
    • Pollock, P.M., Yu, F., Qiu, L., Parsons, P.G. Hayward, N.K. (1995). Evidence for u.v. induction of CDKN2 mutations in melanoma cell lines. Oncogene 11, 663 668.
    • (1995) Oncogene , vol.11 , pp. 663-668
    • Pollock, P.M.1    Yu, F.2    Qiu, L.3    Parsons, P.G.4    Hayward, N.K.5
  • 35
    • 21144439424 scopus 로고    scopus 로고
    • Role of the CDKN2A locus in patients with multiple primary melanomas
    • Puig, S., Malvehy, J., Badenas, C. et al. (2005). Role of the CDKN2A locus in patients with multiple primary melanomas. J. Clin. Oncol. 23, 3043 3051.
    • (2005) J. Clin. Oncol. , vol.23 , pp. 3043-3051
    • Puig, S.1    Malvehy, J.2    Badenas, C.3
  • 36
    • 0038757730 scopus 로고    scopus 로고
    • Role of palmitoylation/depalmitoylation reactions in G-protein-coupled receptor function
    • Qanbar, R. Bouvier, M. (2003). Role of palmitoylation/depalmitoylation reactions in G-protein-coupled receptor function. Pharmacol. Ther. 97, 1 33.
    • (2003) Pharmacol. Ther. , vol.97 , pp. 1-33
    • Qanbar, R.1    Bouvier, M.2
  • 39
    • 27744479216 scopus 로고    scopus 로고
    • Cutaneous melanoma susceptibility and progression genes
    • de Snoo, F.A. Hayward, N.K. (2005). Cutaneous melanoma susceptibility and progression genes. Cancer Lett. 230, 153 186.
    • (2005) Cancer Lett. , vol.230 , pp. 153-186
    • De Snoo, F.A.1    Hayward, N.K.2
  • 41
    • 10744230299 scopus 로고    scopus 로고
    • Germline mutations of the INK4a-ARF gene in patients with suspected genetic predisposition to melanoma
    • Soufir, N., Lacapere, J.J., Bertrand, G. et al. (2004). Germline mutations of the INK4a-ARF gene in patients with suspected genetic predisposition to melanoma. Br. J. Cancer 90, 503 509.
    • (2004) Br. J. Cancer , vol.90 , pp. 503-509
    • Soufir, N.1    Lacapere, J.J.2    Bertrand, G.3
  • 42
    • 33847768225 scopus 로고    scopus 로고
    • A French CDK4-positive melanoma family with a co-inherited EDNRB mutation
    • Soufir, N., Ollivaud, L., Bertrand, G. et al. (2007). A French CDK4-positive melanoma family with a co-inherited EDNRB mutation. J. Dermatol. Sci. 46, 61 64.
    • (2007) J. Dermatol. Sci. , vol.46 , pp. 61-64
    • Soufir, N.1    Ollivaud, L.2    Bertrand, G.3
  • 45
    • 0038457509 scopus 로고    scopus 로고
    • Melanoma etiology: Where are we?
    • Tucker, M.A. Goldstein, A.M. (2003). Melanoma etiology: where are we? Oncogene 22, 3042 3052.
    • (2003) Oncogene , vol.22 , pp. 3042-3052
    • Tucker, M.A.1    Goldstein, A.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.