Variant translocation t(6;10)(p21;q22) in pulmonary chondroid hamartoma

Genes Chromosomes and Cancer

Volumn 15, Issue 4, 1996, Pages 246-248

  Minoletti, Fabiola ^a   Sozzi, Gabriella ^a   Calderone, Caria ^a   Di Palma, Silvana ^a   Pilotti, Silvana ^a   Azzarelli, Alberto ^a   Pierotti, Marco A ^a  

^a NATIONAL CANCER INSTITUTE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CANCER CYTODIAGNOSIS; CHROMOSOME TRANSLOCATION 10; CHROMOSOME TRANSLOCATION 6; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC VARIABILITY; HAMARTOMA; HUMAN; HUMAN CELL; HUMAN TISSUE; LUNG CANCER; PRIORITY JOURNAL;

CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 6; HAMARTOMA; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LUNG; TRANSLOCATION, GENETIC;

EID: 0029995366     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199604)15:4<246::AID-GCC6>3.0.CO;2-1     Document Type: Article

References (14)

1. Dal Cin P, Kools P, De Jonge I, Moerman P, Van de Ven W, Van den Berghe H (1993) Rearrangement of 12q14-15 in pulmonary chrondroid hamartoma. Genes Chromosom Cancer 8:131-133.
2. Fletcher JA, Pinkus GS, Weidner N, Morton CC (1991) Lineage-restricted clonality in biphasic solid tumors. Am J Pathol 138: 1199-1207.
3. Fletcher JA, Pinkus GS, Donovan K, Naeem R, Sugarbaker DJ, Mentzer N, Pinkus JL, Longtine J (1992) Clonal rearrangement of chromosome band 6p21 in the mesenchymal component of pulmonary chondroid hamartoma. Cancer Res 52:6224-6228.
4. Fletcher JA, Longtine J, Wallace K, Mentzer SJ, Sugarbaker DJ (1995) Cytogenetic and histologic findings in 17 pulmonary chondroid hamartomas: evidence for a pathogenetic relationship with lipomas and leiomyomas. Genes Chromosom Cancer 12:220-223.
5. Friedmann M, Holth LT, Zoghbi HY, Reeves R (1993) Organisation, inducible-expression and chromosome localization of the human HMG1(Y) non-histone protein gene. Nucleic Acids Res 21: 4259-4267.
6. Johansson M, Heim S, Mandahl N, Johansson L, Hambraeus G, Mitelman F (1992) t(3;6;14)(p21;p21;q24) as the sole clonal chromosome abnormality in a hamartoma of the lung. Cancer Genet Cytogenet 60:219-220.
7. Johansson M, Dietrich C, Mandahl N, Hambraeus G, Johansson L, Clausen PP, Mitelman K, Heim S (1993) Recombinations of chromosomal hands 6p21 and 14q24 characterise pulmonary hamartomas. Br J Cancer 67:1236-1241.
8. Kazmierczak B, Wanschura S, Rosigkeit J, Meyer-Bolte K, Uschinsky K, Haupt R, Schoenmakers EFPM, Bartnitzke S, Van de Ven WJM, Bullerdiek J (1995) Molecular characterization of 12q14-15 rearrangements in three pulmonary chondroid hamartomas. Cancer Res 55:2497-2499.
9. Klever M, Grond-Ginsbach C, Scherthan H, Schroeder-Kurth TM (1991) Chromosomal in situ suppression hybridization after Giemsa banding. Hum Genet 86:484-486.
10. Miozzo M, Sozzi G, Calderone C, Pilotti S, Lombardi L, Pierotti MA, Delia Porta G (1990) t(11:22) in three cases of peripheral neuroepithelioma. Genes Chromosom Cancer 2:163-165.
11. Ozisik YY, Meloni AM, Altungoz O, Surti U, Sandberg AA (1995) Translocation (6;10)(p21;q22) in uterine leiomyomas. Cancer Genet Cytogenet 79:136-138.
12. Rabbitts TH (1994) Chromosomal translocations in human cancer. Nature 372:143-149.
13. Schoenmakers EFPM, Wanschura S, Mols R, Bullerdiek J, Van den Berghe H, Van de Ven W (1995) Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumours. Nature Genet 10:436-444.
14. Van de Bosch JMM, Wagenaar SS, Corrin B, Elbers JRJ, Knaepen PJ, Westermann CJJ (1987) Mesenchymoma of the lung (so called Hamartoma): a review of 154 parenchymal and endobronchial cases. Thorax 42:790-793.