Comparison of benign and malignant follicular thyroid tumours by comparative genomic hybridization

British Journal of Cancer

Volumn 78, Issue 8, 1998, Pages 1012-1017

  Hemmer, S ^a   Wasenius, V M ^a   Knuutila, S ^a   Joensuu, H ^a   Franssila, K ^a  

^a HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

Author keywords

Adenoma; Carcinoma; Comparative genomic hybridization; DNA sequence; Thyroid

Indexed keywords

ADULT; AGED; ARTICLE; BENIGN TUMOR; CANCER GENETICS; CHROMOSOME 12; CHROMOSOME 14; CHROMOSOME 17; CHROMOSOME 18; CHROMOSOME 22; CHROMOSOME 22Q; CHROMOSOME 5; CHROMOSOME 7; CHROMOSOME 9; CHROMOSOME LOSS; CLINICAL ARTICLE; CONTROLLED STUDY; DNA DETERMINATION; DNA SEQUENCE; FEMALE; FOLLICULAR CARCINOMA; HUMAN; HUMAN TISSUE; MALE; PRIORITY JOURNAL; THYROID ADENOMA; THYROID TUMOR; X CHROMOSOME;

EID: 0031664987     PISSN: 00070920     EISSN: None     Source Type: Journal    
DOI: 10.1038/bjc.1998.620     Document Type: Article

References (30)

1. Antonini P, Lévy N, Caillou B, Vénual A-M, Schlumberger M, Parmentier C and Bernheim A (1993) Numerical aberrations, including trisomy 22 as the sole anomaly, are recurrent in follicular thyroid adenomas. Genes Chrom Cancer 8: 63-66
2. Belge G, Thode B, Rippe V, Bartnizke S and Bullerdiek J (1994) A characteristic sequence of trisomies starting with trisomy 7 in benign thyroid tumours. Hum Genet 94: 198-202
3. Björqkvist A-M, Tammilehto L, Anttila S, Mattson K and Knuutila S (1997) Recurrent DNA copy number changes in 1q, 4q, 6q, 9q, 13q, 14q and 22q detected by comparative genomic hybridization in malignant mesothelioma. Br J Cancer 75: 523-527
4. Bondeson L, Bengtsson A, Bondeson A-G, Dahlenfors R, Grimelius L, Wedell B and Mark J (1989) Chromosome studies in thyroid neoplasia. Cancer 64: 680-685
5. Oriado B, Barros A, Suijkerbuijk RF, Weghuis DO, Seruca R, Fonseca E and Castedo S (1995) Detection of numerical alterations for chromosomes 7 and 12 in benign thyroid lesions by in situ hybridization. Am J Pathol 147: 136-144
6. El-Rifai W, Sarlomo-Rikala M, Miettinen M, Knuutila S and Andersson L (1996) DNA copy number losses in chromosome 14: an early change in gastrointestinal stromal tumours. Cancer Rev 56: 3230-3233
7. El-Rifai W, Larramendy ML, Björkqvist A-M, Hemmer S and Knuutila S (1997) Optimization of comparative genomic hybridization by fluorochrome conjugated to dCTP and dUTP nucleotides. Lab Invest 77: 699-700
8. Franssila K (1997) Thyroid. In Bloodworth's Endocrine Pathology, 3rd edn, Lechago J and Gould VE (eds), pp. 171-247. Williams & Wilkins: Baltimore
9. Grebe SKG, Meiver B, Hay ID, Wu PSC, Maciel LMZ, Drabkin HA, Goellner JR, Grant CS, Jenkins RB and Eberhardt NL (1997) Frequent loss of heterozygosity on chromosomes 3p and 17p without VHL or p53 mutations suggests involvement of unidentified tumor suppressor genes in follicular thyroid carcinoma. J Clin Endocrinol Metab 82: 3684-3691
10. Hedinger CE, Williams ED and Sobin LH (1988) Histological Typing of Thyroid Tumours. Springer Verlag: New York
11. Hedinger C, Williams ED and Sobin LH (1989) The WHO histological classfication of thyroid tumours: a commentary on the second edition. Cancer 63: 908-911
12. Heim S and Mitelman F (1995) Cancer Cytogenet 2nd edn. Wiley-Liss: New York
13. Herrman MA, Hay ID, Bartelt Jr DH, Ritland SR, Dahl RJ, Grant CS and Jenkins RB (1991) Cytogenetic and molecular genetic studies of follicular and papillary thyroid cancers. J Clin Invest 88: 1596-1604
14. Jenkins RB, Hay ID, Herath JF, Schultz CG, Spurbeck JL, Grant CS, Goellner JR and Dewald GW (1990) Frequent occurrence of cytogenetic abnormalities in sporadic non-medullary thyroid carcinoma. Cancer 66: 1213-1220
15. Joensuu H and Klemi PJ (1988) DNA aneuploidy in adenomas of endocrine organs. Am J Pathol 132: 145-151
16. Kallioniemi O-P, Kallioniemi A, Piper J, Isola J, Waldman FM, Gray JW and Pinkel D (1994) Optimizing comparative genomic hyhridization for analysis of DNA sequence copy number changes in solid tumour. Genes Chrom Cancer 10: 231-243
17. Knuutila S, Björkqvist A-M, Autio K, Tarkkanen M, Wolf M, Monni O, Szymanska J, Larramendy ML, Tapper J, Pere H, El-Rifai W, Hemmer S, Wasenius V-M, Vidgren V and Zhu Y (1998) DNA copy number amplifications in human neoplasms - a review of comparative genomic hybridization studies. Am J Pathol 152: 1107-1123
18. Mohapatra G, Kim DH and Feurstein BG (1995) Detection of multiple gains and losses of genetic material in ten glioma cell lines by comparative genomic hybridization. Genes Chrom Cancer 13: 86-93
19. Roque L, Castedo S, Gomes P, Soares P, Clode A and Soares J (1993a) Cytogenetic findings in 18 follicular thyroid adenomas. Cancer Genet Cytogenet 67: 1-6
20. Roque L, Gomes P, Correia C, Soares P, Soares J and Castedo S (1993b) Thyroid nodular hyperplasia: chromosomal studies in 14 cases. Cancer Genet Cytogenet 69: 31-34
21. Roque L, Castedo S, Clode A and Soares J (1993c) Deletion of 3p25-pter in a primary follicular thyroid carcinoma and its metastasis. Genes Chrom Cancer 8: 199-203
22. Ruttledge M, Sarrazin J, Rangaratnam S, Phelan C, Twist E, Merel P, Delattre O, Thomas G, Nordenskjöld M, Collins P, Dumanski J and Rouleau G (1994) Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas. Nature Genet 6: 180-184
23. Sambrook J, Fritisch EF and Maniatis T (1989) Molecular Cloning: a Laboratory Manual. 2nd edn, Cold Spring Harbor Labarotory Press: Cold Spring Harbor, NY
24. Schofield DE, Beckwith JB and Sklar J (1946) Loss of heterozygosity at chromosome regions 22q11-12 and 11p15.5 in renal rhabdoid tumours. Genes Chrom Cancer 15: 10-17
25. Sozzi G, Miozzo M, Cariani TC, Bongarzone I, Pilotti S, Pierotti MA and Della Porta G (1992) A t(2:3)(q12-13:p24-25) in follicular thyroid adenomas. Cancer Genet Cytogenet 64: 38-41
26. Teyssier J-R, Liautaud-Roger F, Ferre D, Patey M and Dufer J (1990) Chromosomal changes in thyroid tumours. Relation with DNA content, karyotypic features, and clinical data. Cancer Genet Cytogenet 50: 249-263
27. Tonk V, Osella P, Delasmorenas A, Wyandt HE and Milunsky A (1992) Abnormalities of chromosome 22 in meningiomas and confirmation of the origin of a dicentric 22 by in situ hybridization. Cancer Genet Cytogenet 64: 65-68
28. van den Berg E, Oosterhuis JW, de Jong B, Buist J, Vos AM, Dam A and Vermeij B (1990) Cytogenetics of thyroid follicular adenomas. Cancer Genet Cytogenet 44: 217-222
29. van den Berg E, van Doormaal JJ, Oosterhuis JW, de Jong B, Wiersema J, Vos AM, Dam A and Vermeij A (1991) Chromosomal aberrations in follicular thyroid carcinoma. Case report of a primary tumor and its metastasis. Cancer Genet Cytogenet 54: 215-222
30. Woolner LB, Beauhrs OH, Black BM, McConahey WM and Keating Jr FR (1961) Classification and prognosis of thyroid carcinoma. Am J Surg 102: 354-387