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Volumn 64, Issue 3, 2005, Pages 132-139

Adrenal pathophysiology: Lessons from the carney complex

Author keywords

Carney complex; Cushing's syndrome; Cyclic AMP; Primary pigmented nodular adrenocortical disease; PRKAR1A gene

Indexed keywords

CORTICOSTEROID; CORTICOTROPIN; CYCLIC AMP; CYCLIC AMP DEPENDENT PROTEIN KINASE; DEXAMETHASONE; PROTEIN SUBUNIT;

EID: 27144504725     PISSN: 03010163     EISSN: None     Source Type: Journal    
DOI: 10.1159/000088586     Document Type: Short Survey
Times cited : (27)

References (31)
  • 1
    • 0022397926 scopus 로고
    • The complex of myxomas, spotty pigmentation, and endocrine overactivity
    • Baltimore
    • Carney JA, Gordon H, Carpenter PC, Shenoy BV, Go VL: The complex of myxomas, spotty pigmentation, and endocrine overactivity. Medicine (Baltimore) 1985;64:270-283.
    • (1985) Medicine , vol.64 , pp. 270-283
    • Carney, J.A.1    Gordon, H.2    Carpenter, P.C.3    Shenoy, B.V.4    Go, V.L.5
  • 2
    • 0021339563 scopus 로고
    • Bilateral primary pigmented nodular adrenocortical disease: Rare cause of the Cushing syndrome
    • Shenoy BV, Carpenter PC, Carney JA: Bilateral primary pigmented nodular adrenocortical disease: rare cause of the Cushing syndrome. Am J Surg Pathol 1984;8:335-344.
    • (1984) Am J Surg Pathol , vol.8 , pp. 335-344
    • Shenoy, B.V.1    Carpenter, P.C.2    Carney, J.A.3
  • 3
    • 80051974356 scopus 로고
    • Primary pigmented nodular adrenocortical disease and its associated conditions
    • Carney JA, Young WF: Primary pigmented nodular adrenocortical disease and its associated conditions. Endocrinologist 1992;2:6-21.
    • (1992) Endocrinologist , vol.2 , pp. 6-21
    • Carney, J.A.1    Young, W.F.2
  • 4
    • 85003136336 scopus 로고
    • Primary adrenocortical nodular dysplasia: A rare cause of Cushing's syndrome
    • Meador CK, Bowdoin B, Owen WC, Farmer TA: Primary adrenocortical nodular dysplasia: a rare cause of Cushing's syndrome. J Clin Endocrinol Metab 1967;27:1255-1263.
    • (1967) J Clin Endocrinol Metab , vol.27 , pp. 1255-1263
    • Meador, C.K.1    Bowdoin, B.2    Owen, W.C.3    Farmer, T.A.4
  • 5
    • 0014860511 scopus 로고
    • La polymicroadénomatose de la cortico-surrénale dans le syndrome de Cushing
    • Paris
    • Bricaire H, Luton JP, Ghozland M, Forest M: La polymicroadé nomatose de la cortico-surrénale dans le syndrome de Cushing. Ann Med Interne (Paris) 1970;121:755-777.
    • (1970) Ann Med Interne , vol.121 , pp. 755-777
    • Bricaire, H.1    Luton, J.P.2    Ghozland, M.3    Forest, M.4
  • 6
    • 0014845799 scopus 로고
    • Etude clinique, biologique et histologique d'un cas exemplaire de polymicroadénomatose cortico-surrénale
    • Paris
    • de Gennes JL, Garnier H, Calmette, Malinsky M, Bertrand C: Etude clinique, biologique et histologique d'un cas exemplaire de polymicroadé nomatose cortico-surrénale. Ann Endocrinol (Paris) 1970;31:1022-1038.
    • (1970) Ann Endocrinol , vol.31 , pp. 1022-1038
    • De Gennes, J.L.1    Garnier, H.2    Calmette3    Malinsky, M.4    Bertrand, C.5
  • 7
    • 0016329949 scopus 로고
    • Severe osteopenia in young adults associated with Cushing's syndrome due to micronodular adrenal disease
    • Ruder HJ, Loriaux DL, Lipsett MB: Severe osteopenia in young adults associated with Cushing's syndrome due to micronodular adrenal disease. J Clin Endocrinol Metab 1974;39:1138-1147.
    • (1974) J Clin Endocrinol Metab , vol.39 , pp. 1138-1147
    • Ruder, H.J.1    Loriaux, D.L.2    Lipsett, M.B.3
  • 8
    • 0030049026 scopus 로고    scopus 로고
    • Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2
    • Stratakis CA, Carney JA, Lin JP, Papanicolaou DA, Karl M, Kastner DL, Pras E, Chrousos GP: Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2. J Clin Invest 1996;97:699-705.
    • (1996) J Clin Invest , vol.97 , pp. 699-705
    • Stratakis, C.A.1    Carney, J.A.2    Lin, J.P.3    Papanicolaou, D.A.4    Karl, M.5    Kastner, D.L.6    Pras, E.7    Chrousos, G.P.8
  • 12
    • 0036736814 scopus 로고    scopus 로고
    • Mutations of the PRKAR1A gene in Cushing's syndrome due to sporadic primary pigmented nodular adrenocortical disease (PPNAD)
    • Groussin L, Jullian E, Perlemoine K, Leheup B, Luton JP, Bertagna X, Bertherat J: Mutations of the PRKAR1A gene in Cushing's syndrome due to sporadic primary pigmented nodular adrenocortical disease (PPNAD). J Clin Endocrinol Metab 2002;87:4324-4329.
    • (2002) J Clin Endocrinol Metab , vol.87 , pp. 4324-4329
    • Groussin, L.1    Jullian, E.2    Perlemoine, K.3    Leheup, B.4    Luton, J.P.5    Bertagna, X.6    Bertherat, J.7
  • 16
    • 0041381386 scopus 로고    scopus 로고
    • Primary pigmented nodular adrenocortical disease: Paradoxical responses of cortisol secretion to dexamethasone occur in vitro and are associated with increased expression of the glucocorticoid receptor
    • Bourdeau I, Lacroix A, Schurch W, Caron P, Antakly T, Stratakis CA: Primary pigmented nodular adrenocortical disease: paradoxical responses of cortisol secretion to dexamethasone occur in vitro and are associated with increased expression of the glucocorticoid receptor. J Clin Endocrinol Metab 2003;88:3931-3937.
    • (2003) J Clin Endocrinol Metab , vol.88 , pp. 3931-3937
    • Bourdeau, I.1    Lacroix, A.2    Schurch, W.3    Caron, P.4    Antakly, T.5    Stratakis, C.A.6
  • 17
    • 0030986161 scopus 로고    scopus 로고
    • Primary pigmented nodular adrenocortical disease: Reevaluation of a patient with Carney complex 27 years after unilateral adrenalectomy
    • Sarlis NJ, Chrousos GP, Doppman JL, Carney JA, Stratakis CA: Primary pigmented nodular adrenocortical disease: reevaluation of a patient with Carney complex 27 years after unilateral adrenalectomy. J Clin Endocrinol Metab 1997;82:1274-1278.
    • (1997) J Clin Endocrinol Metab , vol.82 , pp. 1274-1278
    • Sarlis, N.J.1    Chrousos, G.P.2    Doppman, J.L.3    Carney, J.A.4    Stratakis, C.A.5
  • 18
    • 0034642302 scopus 로고    scopus 로고
    • Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex
    • Kirschner LS, Sandrini F, Monbo J, Lin JP, Carney JA, Stratakis CA: Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the Carney complex. Hum Mol Genet 2000;9:3037-3046.
    • (2000) Hum Mol Genet , vol.9 , pp. 3037-3046
    • Kirschner, L.S.1    Sandrini, F.2    Monbo, J.3    Lin, J.P.4    Carney, J.A.5    Stratakis, C.A.6
  • 19
    • 0036907704 scopus 로고    scopus 로고
    • Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD) reveals novel mutations and clues for pathophysiology
    • Groussin L, Kirschner L, Vincent-Dejean C, Perlemoine K, Jullian E, Delemer B, Zacharieva S, Pignatelli D, Carney JA, Luton JP, Bertagna X, Stratakis CA, Bertherat J: Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD) reveals novel mutations and clues for pathophysiology. Am J Hum Genet 2002;71:1432-1442.
    • (2002) Am J Hum Genet , vol.71 , pp. 1432-1442
    • Groussin, L.1    Kirschner, L.2    Vincent-Dejean, C.3    Perlemoine, K.4    Jullian, E.5    Delemer, B.6    Zacharieva, S.7    Pignatelli, D.8    Carney, J.A.9    Luton, J.P.10    Bertagna, X.11    Stratakis, C.A.12    Bertherat, J.13
  • 24
    • 9444247656 scopus 로고    scopus 로고
    • Minireview: PRKAR1A: normal and abnormal functions
    • Bossis I, Stratakis CA: Minireview: PRKAR1A: normal and abnormal functions. Endocrinology 2004;145:5452-5458.
    • (2004) Endocrinology , vol.145 , pp. 5452-5458
    • Bossis, I.1    Stratakis, C.A.2
  • 25
    • 18944379653 scopus 로고    scopus 로고
    • Frequent germline mutation of the PKA regulatory subunit 1 (PRKAR1A) in patients with Carney complex (CNC) and/or sporadic primary pigmented nodular adrenocortical disease (PPNAD)
    • Lisbon, 0R46
    • Groussin L, René-Corail F, Jullian E, Bertagna X, Bertherat J: Frequent germline mutation of the PKA regulatory subunit 1 (PRKAR1A) in patients with Carney complex (CNC) and/or sporadic primary pigmented nodular adrenocortical disease (PPNAD). 12th Int Congr of Endocrinology, Lisbon, 2004, 0R46, p 110.
    • (2004) 12th Int Congr of Endocrinology , pp. 110
    • Groussin, L.1    René-Corail, F.2    Jullian, E.3    Bertagna, X.4    Bertherat, J.5
  • 26
    • 27144519479 scopus 로고    scopus 로고
    • A low penetrance mutation in the regulatory subunit R1A of the PKA gene (PRKAR1A) responsible for primary pigmented nodular adrenocortical disease (PPNAD) in seven kindreds suggests a genotype/phenotype correlation in Carney complex (CNC)
    • New Orleans, 0R
    • Groussin L, Jullian E, René-Corail F, Lefebvre H, Vantyghem MC, Chanson P, Conte-Devolx B, Bertagna X, Bertherat J: A low penetrance mutation in the regulatory subunit R1A of the PKA gene (PRKAR1A) responsible for primary pigmented nodular adrenocortical disease (PPNAD) in seven kindreds suggests a genotype/phenotype correlation in Carney complex (CNC). Endocr Soc 86th Annu Meet, New Orleans, 2004, 0R, pp 10-15.
    • (2004) Endocr Soc 86th Annu Meet , pp. 10-15
    • Groussin, L.1    Jullian, E.2    René-Corail, F.3    Lefebvre, H.4    Vantyghem, M.C.5    Chanson, P.6    Conte-Devolx, B.7    Bertagna, X.8    Bertherat, J.9
  • 27
    • 0036291366 scopus 로고    scopus 로고
    • Role of the PKA-regulated transcription factor CREB in development and tumorigenesis of endocrine tissues
    • Rosenberg D, Groussin L, Jullian E, Perlemoine K, Bertagna X, Bertherat J: Role of the PKA-regulated transcription factor CREB in development and tumorigenesis of endocrine tissues. Ann N Y Acad Sci 2002;968:65-74.
    • (2002) Ann N Y Acad Sci , vol.968 , pp. 65-74
    • Rosenberg, D.1    Groussin, L.2    Jullian, E.3    Perlemoine, K.4    Bertagna, X.5    Bertherat, J.6
  • 28
    • 0037178847 scopus 로고    scopus 로고
    • Increased basal cAMP-dependent protein kinase activity inhibits the formation of mesoderm-derived structures in the developing mouse embryo
    • Amieux PS, Howe DG, Knickerbocker H, Lee DC, Su T, Laszlo GS, Idzerda RL, McKnight GS: Increased basal cAMP-dependent protein kinase activity inhibits the formation of mesoderm-derived structures in the developing mouse embryo. J Biol Chem 2002;277:27294-27304.
    • (2002) J Biol Chem , vol.277 , pp. 27294-27304
    • Amieux, P.S.1    Howe, D.G.2    Knickerbocker, H.3    Lee, D.C.4    Su, T.5    Laszlo, G.S.6    Idzerda, R.L.7    McKnight, G.S.8
  • 31


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.