Role of chromosome 11 in hereditary and sporadic pituitary tumourigenesis

Frontiers of Hormone Research

Volumn 20, Issue , 1996, Pages 179-193

  Thakker, R V ^a  

^a HAMMERSMITH HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0013473994     PISSN: 03013073     EISSN: None     Source Type: Book Series    
DOI: None     Document Type: Review

References (53)

1. McCarthy MI, Noonan K, Wass JAH, Monson JP: Familial acromegaly: Studies in three families. Clin Endocrinol 1990;32:719-728.
2. Thakker RV: Multiple endocrine neoplastic type 1; in DeGroot LJ, Besser GM, Burger HG, et al (eds): Endocrinology. Philadelphia, Saunders, 1995, pp 2815-2831.
3. Thakker RV, Ponder BAJ: Multiple endocrine neoplasia; in Sheppard MC (ed): Clinical Endocrinology and Metabolism. Molecular Biology and Endocrinology. London, Bailliere Tindall, 1988, vol 2, pp 1031-1067.
4. Wermer P: Gender aspects of adenomatosis of endocrine glands. Am J Med 1954;16:363-371.
5. Sipple JH: The association of pheochromocytoma with carcinoma of the thyroid gland. Am J Med 1961;31:163-166.
6. Schimke RN: Multiple endocrine neoplasia: how many syndromes? Am J Med Genet 1990;37:375-383.
7. Zeller JR, Kauffman HM, Komorowski RA, Itskovitz HD: Bilateral pheochromocytoma and islet cell adenoma of the pancreas. Arch Surg 1982;117:827.
8. Miller GL, Wynn J: Acromegaly, pheochromocytoma, toxic goiter, diabetes mellitus, and endometriosis. Arch Intern Med 1971;127:299-303.
9. Larsson C, Skogseid B, Oberg K, Nakamura Y, Nordenskjold MC: Multiple endocrine neoplasia type I gene maps to chromosome 11 and is lost in insulinoma. Nature 1988;332:85-87.
10. Friedman E, Sakaguchi K, Bale AE, Falchetti A, Streeten E, Zimering MB, Weinstein LS. Norton J A, Aurbach GD, Spiegel AM, Marx SJ: Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1. N Engl J Med 1989;321:213-218.
11. Thakker RV, Bouloux R, Wooding C, Chotai K, Broad PM, Spurr NK, Besser GM, O'Riordan JLH: Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11. N Engl J Med 1989;321:218-224.
12. Thakker RV, Pook MA, Wooding C, Boscaro M, Scanarini M, Clayton RN: Association of somatotrophinomas with loss of alleles on chromosome 11 and gsp mutations. J Clin Invest 1993;91:2815-2821.
13. Boggild MD, Jenkinson S, Pistorello M, Boscaro M, Scanarini M, McTernan P, Perrett CW, Thakker RV, Clayton RN: Molecular genetic studies of sporadic pituitary tumours. J Clin Endocrinol Metab 1994;78:387-392.
14. Varmus HE: The molecular genetics of cellular oncogenes. Annu Rev Genet 1984;18:533-612.
15. Friend SH, Dryja TP, Weinberg RA: Oncogenes and tumour-suppressor genes. N Engl J Med 1988;318:618-622.
16. Ponder B: Gene losses in human tumours. Nature 1988;335:400-402.
17. Dalla-Favera R, Bregni M, Erikson J, Patterson D, Gallo RC, Croce CM: Human c-myc one gene is located on the region of chromosome 8 that is translocated in Burkitt lymphoma cells. Proc Natl Acad Sci USA 1982;79:7824-7827.
18. de Klein A, van Kessel AG, Grosveld G: A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia. Nature 1982;300:765-767.
19. Taub R, Kirsch I, Morton C: Translocation of the c-myc gene into the immunoglobulin heavy chain locus in human Burkitt lymphoma and murine plasmacytoma cells. Proc Natl Acad Sc USA 1982;79:7837-7841.
20. Kurzrock R, Gutterman JN, Talpaz M: The molecular genetics of Philadelphia chromosome-positive leukemias. N Engl J Med 1988;319:990-998.
21. Hansen MF, Cavanee WK: Retinoblastoma and the progression of tumour genetics. Trends Genet 1988;4:125-128.
22. Knudson AG: Mutation and cancer: statistical study of retinoblastoma. Proc Natl Acad Sci USA 1971;68:820-823.
23. Knudson AG, Strong LC, Anderson DE: Heredity and cancer in man. Prog Med Genet 1973;9:113-158.
24. Cavenee WK, Murphree AL, Shull MM: Prediction of familial predisposition to retinoblastoma. N Engl J Med 1986;314:1201-1207.
25. Friend SH, Bernards R, Rogelj S, Weinberg RA, Rapaport JM, Albert DM, Dryja TP: A human DNA segment with properties of the gene that predisposes the retinoblastoma and osteosarcoma. Nature 1986;323:643-646.
26. Thakker RV: The molecular genetics of the multiple endocrine neoplasia syndromes. Clin Endocrinology 1993;38:1-14.
27. Southern EM: Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol 1975;98:503-517.
28. Dryja TP, Rapaport JM, Joyce JM, Petersen RA: Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastoma. Proc Natl Acad Sci USA (1986) 83:7391-7394.
29. Solomon E, Voss R, Hall V: Chromosome 5 allele loss in human colorectal carcinomas. Nature 1987;328:616-619.
30. Stanbridge EJ: Identifying tumor suppressor genes in human colorectal cancer. Science 1990;247:12-13.
31. Fearon ER, Vogelstein B, Feinberg A: Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumour. Nature 1984;309:176-178.
32. Koufos A, Hansen MF, Lampkin BC, Workman ML, Copcland NG, Jenkins NA, Cavenee WK: Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour. Nature 1984;309:170-172.
33. Landis CA, Masters SB, Spada A, Pace AM, Bourne HR, Vallar L: GTPase inhibiting mutations activate the chain of Gs and stimulate adenyl cyclase in human pituitary tumours. Nature 1989;340:692-696.
34. Lyons J, Landis CA, Harsh G, Vallar L, Grunewald K, Feichtinger H, Duh Q-Y, Clark OH, Kawasaki E, Bourne HR, McCormick F: Two G protein oncogenes in human endocrine tumors. Science 1990;249:655-659.
35. Mayer H, Breyel E, Bostock C, Schmidtke J: Assignment of the human parathyroid hormone gene to chromosome 11. Hum Genet 1983;64:283-285.
36. Naylor SL, Sakaguchi AY, Szoka P, Hendy GN, Kronenberg HM, Rich A, Shows TB: Human parathyroid hormone gene (PTH) is on short arm of chromosome 11. Somat Cell Genet 1983;9:609-616.
37. Vasicek TJ, McDeviff BE, Freeman MW, Fennick BJ, Hendy G, Potts JT, Rich A, Kronenberg HM: Nucleotide sequences of the human parathyroid hormone gene. Proc Natl Acad Sci USA 1983;80:2127-2131.
38. Parkinson DB, Thakker RV: A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism. Nature Genet 1992;1:149-152.
39. Arnold A, Staunton CE, Kim HG, Randall DG, Kronenberg HM: Monoclonality and abnormal parathyroid hormone genes in parathyroid adenomas. N Engl J Med 1988;318:658-662.
40. Arnold A, Kim HG, Gaz RD, Eddy RL, Fukushima Y, Byers MG, Shows TB, Kronenberg HM: Molecular cloning and chromosomal mapping of DNA rearranged with the parathyroid hormone gene in a parathyroid adenoma. J Clin Invest 1989;83:2034-2040.
41. Bale AE, Wong E, Arnold A: The parathyroid breakpoint locus on 11q13 maps close to BCL1 and is not a candidate gene for MEN1. Am J Hum Genet 1990;47:A3.
42. Motokura T, Bloom T, Kim HG, Juppner H, Ruderman JV, Kronenberg HM, Arnold A: A novel cyclin encoded by a bcl1 -linked candidate oncogene. Nature 1991;350:512-515.
43. Hunt T: Cell cycle gets more cyclins. Nature 1991;350:462-463.
44. Rosenberg CL, Wong E, Petty EM, Bale AE, Tsujimoto Y, Harris NL, Arnold A: PRAD1, a candidate BCL1 oncogene: Mapping and expression in centrocytic lymphoma. Proc Natl Acad Sci USA 1991;88:9638-9642.
45. Boudi FH, Lothe RA, Taggart RT: Human pepsinogen A (PGA): An informative gene complex located at 11q13. Hum Genet 1990;84:293-295.
46. Thakker RV, Wooding C, Pang J, Farren B, Harding B, Anderson DC, Besser GM, Bouloux P, Brenton DP, Buchanan KD, Edwards CR, Heath DA, Jackson CE, Jansen S, Lips K, Norum RA, Sampson J, Shalet SM, Taggart RT, Tailor D, Wheeler MH, Woollard PM, Yates J: Linkage analysis of 7 polymorphic markers at chromosome 11p11.2-11q13 in 27 multiple endocrine neoplasia type 1 families. Ann Hum Genet 1993;57:17-25.
47. Bystrom C, Larsson C, Blomberg C, Sandelin K, Falkmer U, Skogseid B, Oberg K, Werner S, Nordenskjold M: Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors. Proc Natl Acad Sci USA 1990;87:1968-1972.
48. Yoshimoto K, Iwahana H, Kubo K, Saito S, Itakura M: Allele loss on chromosome 11 in a pituitary tumor from a patient with multiple endocrine neoplasia type 1. Jpn J Cancer Res 1991;82:886-889.
49. Alexander JM, Biller BMK, Bikkal H, Zervas NT, Arnold A, Klibanski A: Clinically nonfunctioning pituitary tumors are monoclonal in origin. J Clin Invest 1990;86:336-340.
50. Herman V, Fagin J, Gonsky R, Kovacs K, Melmed S: Clonal origin of pituitary adenomas. J Clin Endocrinol 1990;71:1427-1433.
51. Vogelstein B, Fearon ER, Hamilton SR: Genetic alterations during colorectal-tumour development. N Engl J Med 1988;319:525-532.
52. Fearon ER, Vogelstein B: A genetic model for colorectal tumorigenesis. Cell 1990;61:759-767.
53. sα gene in non-functioning pituitary tumours. J Clin Endo Metab 1993;77:765-769.