Familial isolated primary hyperparathyroidism with parathyroid carcinomas: Clinical and molecular features

Clinical Endocrinology

Volumn 48, Issue 1, 1998, Pages 67-72

  Yoshimoto, Katsuhiko ^a   Endo, Hideko ^a   Tsuyuguchi, Masaru ^b   Tanaka, Chisato ^a   Kimura, Takehiko ^a   Iwahana, Hiroyuki ^a   Kato, Genichi ^c   Sano, Toshiaki ^a   Itakura, Mitsuo ^a  

^a UNIVERSITY OF TOKUSHIMA   (Japan)

^b TOKUSHIMA PREFECTURAL CENTRAL HOSPITAL   (Japan)

^c KYOTO SECOND RED CROSS HOSPITAL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHROMOSOME 11Q; DNA DETERMINATION; FAMILIAL DISEASE; GENETIC ANALYSIS; GENETIC SUSCEPTIBILITY; HUMAN; MALE; PARATHYROID CARCINOMA; PRIMARY HYPERPARATHYROIDISM; PRIORITY JOURNAL; PROTO ONCOGENE; SCREENING; TUMOR SUPPRESSOR GENE;

ADENOMA; ADULT; CARCINOMA; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; GENETIC MARKERS; HUMANS; HYPERPARATHYROIDISM; LOSS OF HETEROZYGOSITY; MALE; PARATHYROID NEOPLASMS; PEDIGREE;

EID: 0031938392     PISSN: 03000664     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2265.1998.00354.x     Document Type: Article

References (23)

1. Arnold, A. (1994) Molecular mechanisms of parathyroid neoplasia. Endocrinology and Metabolism Clinics of North America, 23, 93-107.
2. Byström, C., Larsson, C., Blomberg, C., Sandelin, K., Falkmer, U., Skogseid, B., Öberg, K., Werner, S. & Nordenskjöld, M. (1990) Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors. Proceedings of National Academy of Sciences USA, 87, 1968-1972.
3. Chandrasekharappa, S.C., Guru, S.C., Manickam, P., Olufemi, S.-C., Collins, F.S., Emmert-Buck, M.R., Debelenko, L.V., Zhuang, Z., Lubensky, I.A., Liotta, L.A., Crabtree, J.S., Wang, Y., Roe, B.A., Weisemann, J., Boguski, M.S., Agarwal, S.K., Kester, M.B., Kim, Y.S., Heppner, C., Dong, Q., Spiegel, A.M., Burns, A.L. & Marx, S.J. (1997) Positional cloning of the gene for multiple endocrine neoplasia-type 1. Science, 276, 404-407.
4. Cryns, V., Thor, A., Xu, H.-J., Hu, S.-E., Wirman, M.E., Vickerry, A.L. Jr, Benedict, W.F. & Arnold, A. (1994) Loss of the retinoblastoma tumor-suppressor gene in parathyroid carcinoma. New England Journal of Medicine, 330, 757-761.
5. Frayha, R.A., Nassar, V.H., Dagher, F. & Salti, I.S. (1972) Familial parathyroid carcinoma. Journal medical Libnais, 25, 299-309.
6. Friedman, E., Sakaguchi, K., Bale, A.E., Falchetti, A., Streeten, E., Zimering, M., Weinstein, L.S., McBride, W.O., Nakamura, Y., Brandi, M.-L., Norton, J.A., Aurbach, G.D., Spiegel, A.M. & Marx, S.J. (1989) Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1. New England Journal of Medicine, 321, 213-218.
7. Friedman, E., Larsson, C., Amorosi, A., Brandi, M.-L., Bale, L.E., Metz, D.C., Jensen, R.T., Skarulis, M.C., Eastmank, R.C., Nieman, L., Norton, J.A. & Marx, S.J. (1994) Multiple endocrine neoplasia type I: pathology, pathophysiology, molecular genetics, and differential diagnosis. In The Parathyroids (eds J.P. Bilezikiam, M. Levine & R. Marcus), pp. 647-680. Raven Press, New York.
8. Gyapay, G., Morissette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernadi, G., Lathrop, M. & Weissenbach, J. (1994) The 1993-94 Généthon human genetic linkage map. Nature Genetics, 7, 246-339.
9. Kassem, M., Zang, X., Brask, S., Eriksen, E.F., Mosekilde, L. & Kruze, T.A. (1994) Familial isolated primary hyperparathyroidism. Clinical Endocrinology, 41, 415-420.
10. Kimura, T., Yoshimoto, K., Tanaka, C., Ohkura, T., Iwahana, H., Miyauchi, A., Sano, T. & Itakura, M. (1996) Obvious mRNA and protein expression but absence of mutations of the RET proto-oncogene in parathyroid tumors. European Journal of Endocrinology, 134, 314-319.
11. Leborgne, J., Le Neel, J.C., Buzelin, F. & Malvy, P. (1975) Cancer familial des parathyroïdes. Intérêt de l'angiographie dans le diagnostic des récidives loco-régionales. Journal de Chirurgie (Paris), 109, 315-326.
12. Lloyd, R.V., Carney, J.A., Ferreiro, J.A., Jin, L., Thompson, G.B., van Heerden, J.A., Grant, C.S. & Wollan, P.C. (1995) Immunohistochemical analysis of the cell cycle-associated antigen Ki-67 and retinoblastoma protein in parathyroid carcinomas and adenomas. Endocrine Pathology, 6, 279-287.
13. Mallette, L.E. (1994) The functional and pathologic spectrum of parathyroid abnormalities in hyperparathyroidism. In The Parathyroids (eds J.P. Bilezikiam, M. Levine & R. Marcus), pp. 423-455. Raven Press, New York.
14. Mulligan, L.M., Kwok, J.B.J., Healey, J.K., Eldson, M.J., Eng, C., Ponder, M.A., Telenius, H., Tunnacliffe, A. & Ponder, B.A.J. (1993) Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature, 363, 458-460.
15. Shintani, Y., Yoshimoto, K., Horie, H., Sano, T., Kanesaki, Y., Hosoi, E., Yokogoshi, Y., Bando, H., Iwahana, H., Kannuki, S., Matsumoto, K., Itakura, M. & Saito, S. (1995) Two different pituitary adenomas in a patient with multiple endocrine neoplasia type 1 associated with growth hormone-releasing hormone-producing pancreatic tumor: clinical and genetic features. Endocrine Journal, 42, 331-340.
16. Streeten, E.A., Weinstein, L.S., Norton, J.A., Mulvihill, J.J., White, B.J., Friedman, E., Jaffe, G., Brandi, M.L., Stewart, K., Zimering, M.B., Spiegel, A.M., Aurbach, G.D. & Marx, S.J. (1992) Studies in a kindred with parathyroid carcinoma. Journal of Clinical Endocrinology and Metabolism, 75, 362-366.
17. Szabò, J., Heath, B., Hill, V.M., Jackson, C.E., Zarbo, R.J., Mallette, L.E., Chew, S.L., Besser, G.M., Thakker, R.V., Huff, V., Leppert, M.F. & Heath, H. III (1995) Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31. American Journal of Human Genetics, 56, 944-950.
18. Tahara, E., Smith, A.P., Gaz, R.D., Cryns, V.L. & Arnold, A. (1996) Genomic localization of novel candidate tumor suppressor gene loci in parathyroid adenomas. Cancer Research, 56, 599-605.
19. Wassif, W.S., Moniz, C.F., Friedman, E., Wong, S., Weber, G., Nordenskjöld, M., Peters, T.J. & Larsson, C. (1993) Familial isolated hyperparathyroidism: a distinct genetic entity with an increased risk of parathyroid cancer. Journal of Clinical Endocrinology and Metabolism, 77, 1485-1489.
20. Wells, S.A. Jr & Donis-Keller, H. (1994) Current perspectives on the diagnosis and management of patients with multiple endocrine neoplasia type 2 syndromes. Endocrinology and metabolism Clinics of North America, 23, 215-228.
21. Wynne, A.G., van Heerden, J., Carney, J.A. & Fitzpatrick, L.A. (1992) Parathyroid carcinoma: clinical and pathologic features in 43 patients. Medicine, 71, 197-205.
22. Yoshimoto, K. & Saito, S. (1991) Clinical characteristics in multiple endocrine neoplasia type 1 in Japan: a review of 106 patients. Folia Endocrinologica, 67, 764-774 (English abstract).
23. Yoshimoto, K., Iwahana, H., Fukuda, A., Sano, T., Saito, S. & Itakura, M. (1992) Role of p53 mutations in endocrine tumorigenesis: mutation detection by polymerase chain reaction-single strand conformation polymorphism. Cancer Research, 52, 5061-5064.