메뉴 건너뛰기




Volumn 48, Issue 8, 1998, Pages 569-574

Genetic alterations in primary and secondary hyperparathyroidism

Author keywords

Genetics; Parathyroid; Primary hyperparathyroidism; Secondary hyperparathyroidism

Indexed keywords

CHROMOSOME 1Q; GENE LOCUS; GENE MUTATION; GENE REARRANGEMENT; HUMAN; HYPERCALCEMIA; HYPOCALCIURIA; JAW TUMOR; ONCOGENE RET; PRIMARY HYPERPARATHYROIDISM; PRIORITY JOURNAL; REVIEW; SECONDARY HYPERPARATHYROIDISM;

EID: 0031661755     PISSN: 13205463     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1440-1827.1998.tb03952.x     Document Type: Review
Times cited : (8)

References (55)
  • 1
    • 0028946265 scopus 로고
    • Monoclonality of parathyroid tumors in chronic renal failure and in primary parathyroid hyperplasia
    • Arnold A, Brown MF, Urea P et al. Monoclonality of parathyroid tumors in chronic renal failure and in primary parathyroid hyperplasia. J. Clin. Invest. 1995; 95: 2047-2053.
    • (1995) J. Clin. Invest. , vol.95 , pp. 2047-2053
    • Arnold, A.1    Brown, M.F.2    Urea, P.3
  • 3
    • 0013503352 scopus 로고    scopus 로고
    • Molecular basis of hyperparathyroidism
    • Tahara H, Arnold A. Molecular basis of hyperparathyroidism. J. Bone Miner. Metab. 1997; 15: 173-178.
    • (1997) J. Bone Miner. Metab. , vol.15 , pp. 173-178
    • Tahara, H.1    Arnold, A.2
  • 4
    • 0029887858 scopus 로고    scopus 로고
    • Primary hyperparathyroidism: Genetic heterogeneity suggesting different pathogenesis in sporadic and familial forms of parathyroid hyperplasia and tumors
    • Calender A, Cougard P. Primary hyperparathyroidism: Genetic heterogeneity suggesting different pathogenesis in sporadic and familial forms of parathyroid hyperplasia and tumors. Eur. J. Endocrinol. 1996; 134: 263-266.
    • (1996) Eur. J. Endocrinol. , vol.134 , pp. 263-266
    • Calender, A.1    Cougard, P.2
  • 5
    • 0031045242 scopus 로고    scopus 로고
    • Differential loss of heterozygosity in familial, sporadic and uremic hyperparathyroidism
    • Farnebo F, Teh BT, Dotzenrath C et al. Differential loss of heterozygosity in familial, sporadic and uremic hyperparathyroidism. Hum. Genet. 1997; 99: 342-349.
    • (1997) Hum. Genet. , vol.99 , pp. 342-349
    • Farnebo, F.1    Teh, B.T.2    Dotzenrath, C.3
  • 7
    • 0023863047 scopus 로고
    • Monoclonality and abnormal parathyroid hormone genes in parathyroid adenomas
    • Arnold A, Staunton CE, Kim HG et al. Monoclonality and abnormal parathyroid hormone genes in parathyroid adenomas. N. Engl. J. Med. 1988; 318: 658-662.
    • (1988) N. Engl. J. Med. , vol.318 , pp. 658-662
    • Arnold, A.1    Staunton, C.E.2    Kim, H.G.3
  • 8
    • 0030950461 scopus 로고    scopus 로고
    • Comparative analysis of clonality and pathology in primary and secondary hyperparathyroidism
    • Shan L, Nakamura M, Nakamura Y et al. Comparative analysis of clonality and pathology in primary and secondary hyperparathyroidism. Virchows Arch. 1997; 430: 247-251.
    • (1997) Virchows Arch. , vol.430 , pp. 247-251
    • Shan, L.1    Nakamura, M.2    Nakamura, Y.3
  • 9
    • 10544249869 scopus 로고    scopus 로고
    • Allelic deletions on chromosome 11q13 in multiple tumors from individual MEN 1 patients
    • Lubensky IA, Debelenko LV, Zhuang Z et al. Allelic deletions on chromosome 11q13 in multiple tumors from individual MEN 1 patients. Cancer Res. 1996; 56: 5272-5278.
    • (1996) Cancer Res. , vol.56 , pp. 5272-5278
    • Lubensky, I.A.1    Debelenko, L.V.2    Zhuang, Z.3
  • 10
    • 0024399727 scopus 로고
    • Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1
    • Friedman E, Sakaguchi K, Bale AE et al. Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1. N. Engl. J. Med. 1989; 321: 213-218.
    • (1989) N. Engl. J. Med. , vol.321 , pp. 213-218
    • Friedman, E.1    Sakaguchi, K.2    Bale, A.E.3
  • 11
    • 0028316834 scopus 로고
    • Clonal analysis of parathyroid adenomas by means of the polymerase chain reaction
    • Noguchi S, Motomura K, Inaji H, Imaoka S, Koyama H. Clonal analysis of parathyroid adenomas by means of the polymerase chain reaction. Cancer Lett. 1994; 78: 93-97.
    • (1994) Cancer Lett. , vol.78 , pp. 93-97
    • Noguchi, S.1    Motomura, K.2    Inaji, H.3    Imaoka, S.4    Koyama, H.5
  • 12
    • 0029808104 scopus 로고    scopus 로고
    • Clonal analysis of nodular parathyroid hyperplasia in renal hyperparathyroidism
    • Tominaga Y, Kohara S, Namii Y. Clonal analysis of nodular parathyroid hyperplasia in renal hyperparathyroidism. World J. Surg. 1996; 20: 744-752.
    • (1996) World J. Surg. , vol.20 , pp. 744-752
    • Tominaga, Y.1    Kohara, S.2    Namii, Y.3
  • 13
    • 0013502430 scopus 로고    scopus 로고
    • Clonality of the parathyroid nodules with uremic parathyroid hyperplasia
    • Shan L, Kakudo K, Nakamura M et al. Clonality of the parathyroid nodules with uremic parathyroid hyperplasia. Pathol. Oncol. Res. 1997; 3: 198-203.
    • (1997) Pathol. Oncol. Res. , vol.3 , pp. 198-203
    • Shan, L.1    Kakudo, K.2    Nakamura, M.3
  • 14
    • 0017105982 scopus 로고
    • Clonal origin of human tumors
    • Fialkow PJ. Clonal origin of human tumors. Biochim. Biophys. Acta 1976; 458: 283-321.
    • (1976) Biochim. Biophys. Acta , vol.458 , pp. 283-321
    • Fialkow, P.J.1
  • 15
    • 0029057197 scopus 로고
    • Clonality of thyroid nodules in sporadic goiter
    • Apel RL, Ezzat S, Bapat BV et al. Clonality of thyroid nodules in sporadic goiter. Diagn. Mol. Pathol. 1995; 4: 113-121.
    • (1995) Diagn. Mol. Pathol. , vol.4 , pp. 113-121
    • Apel, R.L.1    Ezzat, S.2    Bapat, B.V.3
  • 16
    • 0027421796 scopus 로고
    • Morphological and functional polymorphism within clonal thyroid nodules
    • Aeschimann S, Kopp PA, Kimura ED et al. Morphological and functional polymorphism within clonal thyroid nodules. J. Clin. Endocrinol. Metab. 1993; 77: 846-851.
    • (1993) J. Clin. Endocrinol. Metab. , vol.77 , pp. 846-851
    • Aeschimann, S.1    Kopp, P.A.2    Kimura, E.D.3
  • 17
    • 0027434702 scopus 로고
    • Progression of uremic hyperparathyroidism involves allelic loss on chromosome 11
    • Falchetti A, Bale AE, Amorosi A et al. Progression of uremic hyperparathyroidism involves allelic loss on chromosome 11. J. Clin. Endocrinol. Metab. 1993; 76: 139-144.
    • (1993) J. Clin. Endocrinol. Metab. , vol.76 , pp. 139-144
    • Falchetti, A.1    Bale, A.E.2    Amorosi, A.3
  • 18
    • 0027014449 scopus 로고
    • Parathyroid tumor biology in familial multiple endocrine neoplasia type 1: A model for cancer development
    • Brandi ML. Parathyroid tumor biology in familial multiple endocrine neoplasia type 1: A model for cancer development. Henry Ford Hosp. Med. J. 1992; 40: 181-185.
    • (1992) Henry Ford Hosp. Med. J. , vol.40 , pp. 181-185
    • Brandi, M.L.1
  • 19
    • 0031002034 scopus 로고    scopus 로고
    • Evidence for monoclonal expansion of epithelial cells in ovarian endometrial cysts
    • Jimbo H, Hitomi Y, Yoshikawa H et al. Evidence for monoclonal expansion of epithelial cells in ovarian endometrial cysts. Am. J. Pathol. 1997; 150: 1173-1178.
    • (1997) Am. J. Pathol. , vol.150 , pp. 1173-1178
    • Jimbo, H.1    Hitomi, Y.2    Yoshikawa, H.3
  • 20
    • 0031055032 scopus 로고    scopus 로고
    • Multiple hyperplastic polyps in the stomach: Evidence for clonality and neoplastic potential
    • Dijkhuizen SM, Entius MM, Clement MJ et al. Multiple hyperplastic polyps in the stomach: Evidence for clonality and neoplastic potential. Gastroenterology 1997; 112: 561-566.
    • (1997) Gastroenterology , vol.112 , pp. 561-566
    • Dijkhuizen, S.M.1    Entius, M.M.2    Clement, M.J.3
  • 21
    • 0023828816 scopus 로고
    • Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma
    • Larsson C, Skogseid B; Öberg K et al. Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma. Nature 1988; 332: 85-87.
    • (1988) Nature , vol.332 , pp. 85-87
    • Larsson, C.1    Skogseid, B.2    Öberg, K.3
  • 22
    • 0030963446 scopus 로고    scopus 로고
    • Positional cloning of the gene for multiple endocrine neoplasia-type 1
    • Chandrasekharappa SC, Gurum SC, Manickam P et al. Positional cloning of the gene for multiple endocrine neoplasia-type 1. Science 1997; 276: 404-407.
    • (1997) Science , vol.276 , pp. 404-407
    • Chandrasekharappa, S.C.1    Gurum, S.C.2    Manickam, P.3
  • 23
    • 8544266010 scopus 로고    scopus 로고
    • Identification of the multiple endocrine neoplasia type 1 (MEN 1) gene
    • The European Consortium on MEN 1. Identification of the multiple endocrine neoplasia type 1 (MEN 1) gene. Hum. Mol. Genet. 1997; 6: 1177-1183.
    • (1997) Hum. Mol. Genet. , vol.6 , pp. 1177-1183
  • 24
    • 8544279953 scopus 로고    scopus 로고
    • Germline mutations of the MEN 1 gene in familial multiple endocrine neoplasia type 1 and related states
    • Agarwal SK, Kester MB, Debelenko LV et al. Germline mutations of the MEN 1 gene in familial multiple endocrine neoplasia type 1 and related states. Hum. Mol. Genet. 1997; 6: 1169-1175.
    • (1997) Hum. Mol. Genet. , vol.6 , pp. 1169-1175
    • Agarwal, S.K.1    Kester, M.B.2    Debelenko, L.V.3
  • 25
    • 0005485615 scopus 로고    scopus 로고
    • Germline mutations of MEN 1 gene in Japanese kindred with multiple endocrine neoplasia type 1
    • Shimizu S, Tsukada T, Futami H et al. Germline mutations of MEN 1 gene in Japanese kindred with multiple endocrine neoplasia type 1. Jpn. J. Cancer Res. 1997; 88: 1029-1032.
    • (1997) Jpn. J. Cancer Res. , vol.88 , pp. 1029-1032
    • Shimizu, S.1    Tsukada, T.2    Futami, H.3
  • 26
    • 0030040625 scopus 로고    scopus 로고
    • Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas
    • Tahara H, Smith AP, Gas RD, Cryns VL, Arnold A. Genomic localization of novel candidate tumor suppressor gene loci in human parathyroid adenomas. Cancer Res. 1996; 56: 599-605.
    • (1996) Cancer Res. , vol.56 , pp. 599-605
    • Tahara, H.1    Smith, A.P.2    Gas, R.D.3    Cryns, V.L.4    Arnold, A.5
  • 27
    • 0030755071 scopus 로고    scopus 로고
    • Somatic mutation of the MEN 1 gene in parathyroid tumors
    • Heppner C, Kester MB, Agarwal SK et al. Somatic mutation of the MEN 1 gene in parathyroid tumors. Nature Genet. 1997; 16: 375-378.
    • (1997) Nature Genet. , vol.16 , pp. 375-378
    • Heppner, C.1    Kester, M.B.2    Agarwal, S.K.3
  • 28
    • 0027081143 scopus 로고
    • Allelic loss from chromosome 11 in parathyroid tumors
    • Friedman E, DeMarco L, Gejman PV et al. Allelic loss from chromosome 11 in parathyroid tumors. Cancer Res. 1992; 52: 6804-6809.
    • (1992) Cancer Res. , vol.52 , pp. 6804-6809
    • Friedman, E.1    DeMarco, L.2    Gejman, P.V.3
  • 29
    • 14444284949 scopus 로고    scopus 로고
    • Somatic mutations of MEN 1 gene in the sporadic endocrine tumors
    • in press
    • Shan L, Nakamura Y, Nakamura M et al. Somatic mutations of MEN 1 gene in the sporadic endocrine tumors. Lab. Invest. 1998 (in press).
    • (1998) Lab. Invest.
    • Shan, L.1    Nakamura, Y.2    Nakamura, M.3
  • 30
  • 31
    • 0028981523 scopus 로고
    • Absence of cyclin D1/PRAD 1 point mutations in human breast cancers and parathyroid adenomas and identification of a new cyclin D1 gene polymorphism
    • Hosokawa Y, Tu T, Tahara H, Smith AP, Arnold A. Absence of cyclin D1/PRAD 1 point mutations in human breast cancers and parathyroid adenomas and identification of a new cyclin D1 gene polymorphism. Cancer Lett. 1995; 93: 165-170.
    • (1995) Cancer Lett. , vol.93 , pp. 165-170
    • Hosokawa, Y.1    Tu, T.2    Tahara, H.3    Smith, A.P.4    Arnold, A.5
  • 32
    • 0029940779 scopus 로고    scopus 로고
    • Cyclin D1/PRAD1 expression in parathyroid adenomas: An immunohistochemical study
    • Hsi ED, Zukerberg LR, Yang WI et al. Cyclin D1/PRAD1 expression in parathyroid adenomas: An immunohistochemical study. J. Clin. Endocrinol. Metab. 1996; 81: 1736-1739.
    • (1996) J. Clin. Endocrinol. Metab. , vol.81 , pp. 1736-1739
    • Hsi, E.D.1    Zukerberg, L.R.2    Yang, W.I.3
  • 34
    • 0025876591 scopus 로고
    • The p53 tumor suppressor gene
    • Levine AJ, Momand J, Finlay CA. The p53 tumor suppressor gene. Nature 1991; 351: 453-456.
    • (1991) Nature , vol.351 , pp. 453-456
    • Levine, A.J.1    Momand, J.2    Finlay, C.A.3
  • 35
    • 19244364427 scopus 로고    scopus 로고
    • Allelic loss of the retinoblastoma tumor suppressor gene: A marker for aggressive parathyroid tumors?
    • Dotzenrath C, Teh BT, Farnebo F et al. Allelic loss of the retinoblastoma tumor suppressor gene: A marker for aggressive parathyroid tumors? J. Clin. Endocrinol. Metab. 1996; 81: 3194-3196.
    • (1996) J. Clin. Endocrinol. Metab. , vol.81 , pp. 3194-3196
    • Dotzenrath, C.1    Teh, B.T.2    Farnebo, F.3
  • 36
    • 0028204821 scopus 로고
    • Loss of the retinoblastoma tumor suppressor gene in parathyroid carcinoma
    • Cryns VL, Thor AD, Xu H-J et al. Loss of the retinoblastoma tumor suppressor gene in parathyroid carcinoma. N. Engl. J. Med. 1994; 330: 757-761.
    • (1994) N. Engl. J. Med. , vol.330 , pp. 757-761
    • Cryns, V.L.1    Thor, A.D.2    Xu, H.-J.3
  • 39
    • 0026792908 scopus 로고
    • Role of p53 mutations in endocrine tumorigenesis: Mutation detection by polymerase chain reaction-single strand conformation polymorphism
    • Yoshimoto K, Iwahana H, Fukuda A et al. Role of p53 mutations in endocrine tumorigenesis: Mutation detection by polymerase chain reaction-single strand conformation polymorphism. Cancer Res. 1992; 52: 5061-5064.
    • (1992) Cancer Res. , vol.52 , pp. 5061-5064
    • Yoshimoto, K.1    Iwahana, H.2    Fukuda, A.3
  • 40
    • 0027228517 scopus 로고
    • Histopathological variables and DNA cytometry in parathyroid carcinoma
    • Bondeson L, Sandelin K, Grimelius L. Histopathological variables and DNA cytometry in parathyroid carcinoma. Am. J. Surg. Pathol. 1993; 17: 820-829.
    • (1993) Am. J. Surg. Pathol. , vol.17 , pp. 820-829
    • Bondeson, L.1    Sandelin, K.2    Grimelius, L.3
  • 41
    • 0024208663 scopus 로고
    • Cloning and expression of the ret proto-oncogene encoding a tyrosine kinase with two potential transmembrane domains
    • Takahashi M, Buma Y, Iwamoto T et al. Cloning and expression of the ret proto-oncogene encoding a tyrosine kinase with two potential transmembrane domains. Oncogene 1988; 3: 571-578.
    • (1988) Oncogene , vol.3 , pp. 571-578
    • Takahashi, M.1    Buma, Y.2    Iwamoto, T.3
  • 42
    • 0029450315 scopus 로고
    • RET proto-oncogene mutations and rearrangements in endocrine diseases
    • Lioyd RV. RET proto-oncogene mutations and rearrangements in endocrine diseases. Am. J. Pathol. 1995; 147: 1539-1544.
    • (1995) Am. J. Pathol. , vol.147 , pp. 1539-1544
    • Lioyd, R.V.1
  • 43
    • 0028866313 scopus 로고
    • Absence of ret proto-oncogene point mutations in sporadic hyperplastic and neoplastic lesions of the parathyroid gland
    • Padberg B-C, Schroder S, Jochum W et al. Absence of ret proto-oncogene point mutations in sporadic hyperplastic and neoplastic lesions of the parathyroid gland. Am. J. Pathol. 1995; 147: 1600-1607.
    • (1995) Am. J. Pathol. , vol.147 , pp. 1600-1607
    • Padberg, B.-C.1    Schroder, S.2    Jochum, W.3
  • 45
    • 0029969213 scopus 로고    scopus 로고
    • Obvious mRNA and protein expression but absence of mutations of the ret proto-oncogene in parathyroid tumors
    • Kimura T, Yoshimoto K, Tanaka C et al. Obvious mRNA and protein expression but absence of mutations of the ret proto-oncogene in parathyroid tumors. Eur. J. Endocrinol. 1996; 134: 314-319.
    • (1996) Eur. J. Endocrinol. , vol.134 , pp. 314-319
    • Kimura, T.1    Yoshimoto, K.2    Tanaka, C.3
  • 46
    • 0027787680 scopus 로고
    • Mutations in the human calcium-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
    • Pollak MR, Brown EM, Chou Y-HW et al. Mutations in the human calcium-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Cell 1993; 75: 1297-1303.
    • (1993) Cell , vol.75 , pp. 1297-1303
    • Pollak, M.R.1    Brown, E.M.2    Chou, Y.-H.W.3
  • 47
    • 0028802374 scopus 로고
    • Genetic abnormalities in sporadic parathyroid adenomas: Loss of heterozygosity for chromosome 3q markers flanking the calcium receptor locus
    • Thompson DB, Samowitz WS, Odelberg S et al. Genetic abnormalities in sporadic parathyroid adenomas: Loss of heterozygosity for chromosome 3q markers flanking the calcium receptor locus. J. Clin. Endocrinol. Metab. 1995; 80: 3377-3380.
    • (1995) J. Clin. Endocrinol. Metab. , vol.80 , pp. 3377-3380
    • Thompson, D.B.1    Samowitz, W.S.2    Odelberg, S.3
  • 49
    • 0028958106 scopus 로고
    • Hereditary hyperparathyroidism-jaw tumor syndrome: The endocrine tumor gene HRPT2 maps to chromosome 1q21-q23
    • Szabó J, Heath B, Hill VM et al. Hereditary hyperparathyroidism-jaw tumor syndrome: The endocrine tumor gene HRPT2 maps to chromosome 1q21-q23. Am. J. Hum. Genet. 1995; 56: 944-950.
    • (1995) Am. J. Hum. Genet. , vol.56 , pp. 944-950
    • Szabó, J.1    Heath, B.2    Hill, V.M.3
  • 50
    • 1842403802 scopus 로고    scopus 로고
    • Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney diseases: Linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas
    • Teh BT, Farnebo F, Kristoffersson U et al. Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney diseases: Linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas. J. Clin. Endocrinol. Metab. 1996; 81: 4204-4211.
    • (1996) J. Clin. Endocrinol. Metab. , vol.81 , pp. 4204-4211
    • Teh, B.T.1    Farnebo, F.2    Kristoffersson, U.3
  • 51
    • 0029010785 scopus 로고
    • Frequent loss of chromosome arm 1p DNA in parathyroid adenomas
    • Cryns VL, Yi, SM, Tahara H et al. Frequent loss of chromosome arm 1p DNA in parathyroid adenomas. Genes Chromosomes Cancer 1995; 13: 9-17.
    • (1995) Genes Chromosomes Cancer , vol.13 , pp. 9-17
    • Cryns, V.L.1    Yi, S.M.2    Tahara, H.3
  • 53
    • 0027325891 scopus 로고
    • Rare mutations of the Gs alpha subunit gene in human endocrine tumors
    • Yoshimoto K, Iwahana H, Fukuda A, Sano T, Itakura M. Rare mutations of the Gs alpha subunit gene in human endocrine tumors. Cancer 1993; 72: 1386-1393.
    • (1993) Cancer , vol.72 , pp. 1386-1393
    • Yoshimoto, K.1    Iwahana, H.2    Fukuda, A.3    Sano, T.4    Itakura, M.5
  • 54
    • 0028148560 scopus 로고
    • Absence of mutations in the Gs alpha and Gi2 alpha genes in sporadic parathyroid adenomas and insulinomas
    • Vessey SJ, Jones PM, Wallis SC, Schofield J, Bloom SR. Absence of mutations in the Gs alpha and Gi2 alpha genes in sporadic parathyroid adenomas and insulinomas. Clin. Sci. (Colch.) 1994; 87: 493-497.
    • (1994) Clin. Sci. (Colch.) , vol.87 , pp. 493-497
    • Vessey, S.J.1    Jones, P.M.2    Wallis, S.C.3    Schofield, J.4    Bloom, S.R.5
  • 55
    • 0029836726 scopus 로고    scopus 로고
    • Loss of chromosome arm 9p DNA and analysis of the p16 and p15 cyclin-dependent kinase inhibitor genes in human parathyroid adenomas
    • Tahara H, Smith AP, Gaz RD et al. Loss of chromosome arm 9p DNA and analysis of the p16 and p15 cyclin-dependent kinase inhibitor genes in human parathyroid adenomas. J. Clin. Endocrinol. Metab. 1996; 81: 3663-3667.
    • (1996) J. Clin. Endocrinol. Metab. , vol.81 , pp. 3663-3667
    • Tahara, H.1    Smith, A.P.2    Gaz, R.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.