Letter to the Editors
Der(16)t(1;16) is a secondary chromosome aberration in at least eighteen different types of human cancer
Krzysztof Mrózek,
Clara D. Bloomfield,
Corresponding Author
Krzysztof Mrózek
Division of Hematology and Oncology and the Comprehensive Cancer Center Ohio State University Columbus, Ohio
Division of Hematology and Oncology and the Comprehensive Cancer Center Ohio State University Columbus, OhioSearch for more papers by this authorClara D. Bloomfield
Division of Hematology and Oncology and the Comprehensive Cancer Center Ohio State University Columbus, Ohio
Search for more papers by this authorKrzysztof Mrózek,
Clara D. Bloomfield,
Corresponding Author
Krzysztof Mrózek
Division of Hematology and Oncology and the Comprehensive Cancer Center Ohio State University Columbus, Ohio
Division of Hematology and Oncology and the Comprehensive Cancer Center Ohio State University Columbus, OhioSearch for more papers by this authorClara D. Bloomfield
Division of Hematology and Oncology and the Comprehensive Cancer Center Ohio State University Columbus, Ohio
Search for more papers by this authorFirst published: 07 December 1998
Citations: 14
No abstract is available for this article.
References
- Betts DR, Leibundgut KE, Niggli FK (1996) Cytogenetic analysis in a case of intraocular medulloepithelioma. Cancer Genet Cyto-genet 92: 144–146.
- Betts DR, Koesters R, Plüss H-J, Niggli FK (1997) Routine karyotyping in Wilms' tumor. Cancer Genet Cytogenet 96: 151–156.
- Brigaudeau C, Trimoreau F, Gachard N, Rouzier E, Jaccard A, Bordessoule D, Praloran V (1997) Cytogenetic study of 30 patients with multiple myeloma: Comparison of 3– and 6–day bone marrow cultures stimulated or not with cytokines by using a miniaturized karyotypic method. Br J Haematol 96: 594–600.
- Dal Cin P, Dei Tos AP, Qi H, Giannini C, Furlanetto A, Longatti PL, Marynen P, Van den Berghe H (1998) Immature teratoma of the pineal gland with isochromosome 12p. Acta Neuropathol 95: 107–110.
-
Day SJ,
Nelson M,
Rosenthal H,
Vergara GG,
Bridge JA
(1997)
Der(16)t(1;16)(q21;q13) as a secondary structural aberration in yet a third sarcoma, extraskeletal myxoid chondrosarcoma.
Genes Chromosomes Cancer
20:
425–427.
10.1002/(SICI)1098-2264(199712)20:4<425::AID-GCC16>3.0.CO;2-L CAS PubMed Web of Science® Google Scholar
- Dietrich CU, Pandis N, Teixeira MR, Bardi G, Gerdes A-M, Andersen JA, Heim S (1995) Chromosome abnormalities in benign hyperproliferative disorders of epithelial and stromal breast tissue. Int J Cancer 60: 49–53.
- Flactif M, Laï JL, Zandecki M, Bernardi F, Trillot N, Bauters F, Facon T (1994) Two cases of t(1;16)(p11;p11) in multiple myeloma: Confirmation by chromosome painting. Cancer Genet Cytogenet 76: 10–14.
- Fletcher JA, Aster JC, Morton CC (1989) Association of trisomy 8 and squamous differentiation in an endometrial adenocarcinoma. Cancer Genet Cytogenet 39: 185–189.
- Gibas Z, Miettinen M, Limon J, Nedoszytko B, Mrózek K, Rosz-kiewicz A, Rys J, Niezabitowski A, Debiec-Rychter M (1995) Cytogenetic and immunohistochemical profile of myxoid liposarcoma. Am J Clin Pathol 103: 20–26.
-
Hattinger CM,
Rumpler S,
Ambros IM,
Strehl S,
Lion T,
Zoubek A,
Gadner H,
Ambros PF
(1996)
Demonstration of the translocation der(16)t(1;16)(q12;q11.2) in interphase nuclei of Ewing tumors.
Genes Chromosomes Cancer
17:
141–150.
10.1002/(SICI)1098-2264(199611)17:3<141::AID-GCC1>3.0.CO;2-4 CAS PubMed Web of Science® Google Scholar
- Heim S, Mitelman F (1995) Cancer Cytogenetics, 2nd edit. New York: Wiley-Liss.
- Hindkjaer J, Hammoudah SAFM, Bendix Hansen K, Jensen PD, Koch J, Pedersen B (1995) Translocation (1;16) identified by chromosome painting, and primed in situ-labeling (PRINS). Cancer Genet Cytogenet 79: 15–20.
-
Johansson B,
Mertens F,
Mitelman F
(1996)
Primary vs. secondary neoplasia-associated chromosomal abnormalities: Balanced rearrangements vs. genomic imbalances?
Genes Chromosomes Cancer
16:
155–163.
10.1002/(SICI)1098-2264(199607)16:3<155::AID-GCC1>3.0.CO;2-Y CAS PubMed Web of Science® Google Scholar
- Kees UR, Spagnolo D, Hallam LA, Ford J, Ranford PR, Baker DL, Callen DF, Biegel JA (1998) A new pineoblastoma cell line, PER-480, with der(10)t(10;17), der(16)t(1;16), and enhanced MYC expression in the absence of gene amplification. Cancer Genet Cytogenet 100: 159–164.
- Kokalj-Vokac N, Alemeida A, Gerbault-Seureau M, Malfoy B, Dutrillaux B (1993) Two-color FISH characterization of i(1q) and der(1;16) in human breast cancer cells. Genes Chromosomes Cancer 7: 8–14.
-
Mathew P,
Douglass EC,
Jones D,
Valentine M,
Valentine V,
Rowe S,
Shapiro DN
(1996)
Der(16)t(1;16)(q21;q13) in Wilms' tumor: Friend or foe.
Med Pediatr Oncol
27:
3–7.
10.1002/(SICI)1096-911X(199607)27:1<3::AID-MPO2>3.0.CO;2-K CAS PubMed Web of Science® Google Scholar
- McManus AP, Min T, Swansbury GJ, Gusterson BA, Pinkerton CR, Shipley JM (1996) Der(16)t(1;16)(q21;q13) as a secondary change in alveolar rhabdomyosarcoma. Cancer Genet Cytogenet 87: 179–181.
- Mrózek K, Bloomfield CD (1996) New recurrent structural chromosome aberrations in non-Hodgkin lymphoma: A review of the published literature. Int J Oncol 8: 851–858.
- Mrózek K, Arthur DC, Karakousis CP, Koduru PRK, Le Beau MM, Pettenati MJ, Tantravahi R, Mrózek E, Perez-Mesa C, Rao UNM, Frankel SR, Davey FR, Bloomfield CD (1995) Der(16)t(1;16) is a nonrandom secondary chromosome aberration in many types of human neoplasia, including myxoid liposarcoma, rhabdomyosarcoma and Philadelphia chromosome-positive acute lymphoblastic leukemia. Int J Oncol 6: 531–538.
- Mugneret F, Sidaner I, Favre B, Manone L, Maynadié M, Caillot D, Solary E (1995a) Der(16)t(1;16)(q10;p10) in multiple myeloma: A new non-random abnormality that is frequently associated with Burkitt's-type translocations. Leukemia 9: 277–281.
- Mugneret F, Dastugue N, Favre B, Sidaner I, Salles B, Huguet-Rigal F, Solary E (1995b) Der(16) t(1;16)(q11;q11) in myelodysplastic syndromes: A new non-random abnormality characterized by cytogenic and fluorescence in situ hybridization studies. Br J Haematol 90: 119–124.
- Pandis N, Jin Y, Gorunova L, Petersson C, Bardi G, Idvall I, Johansson B, Ingvar C, Mandahl N, Mitelman F, Heim S (1995a) Chromosome analysis of 97 primary breast carcinomas: Identification of eight karyotypic subgroups. Genes Chromosomes Cancer 12: 173–185.
-
Pandis N,
Teixeira MR,
Gerdes A-M,
Limon J,
Bardi G,
Andersen JA,
Idvall I,
Mandahl N,
Mitelman F,
Heim S
(1995b)
Chromosome abnormalities in bilateral breast carcinomas: Cytogenetic evaluation of the clonal origin of multiple primary tumors.
Cancer
76:
250–258.
10.1002/1097-0142(19950715)76:2<250::AID-CNCR2820760215>3.0.CO;2-W CAS PubMed Web of Science® Google Scholar
- Sawyer JR, Tricot G, Mattox S, Jagannath S, Barlogie B (1998) Jumping translocations of chromosome 1q in multiple myeloma: Evidence for a mechanism involving decondensation of pericentromeric heterochromatin. Blood 91: 1732–1741.
- Schnittger S, Kinkelin U, Schoch C, Haase D, Haferlach T, Löffler H, Wörmann B, Hiddemann W, Greisinger F (1997) Screening for partial tandem duplication within the MLL-gene in patients with acute myeloid leukemia. Blood 90 (suppl 1): 557a.
- Slater HR, Tiong T, Konstantakopoulos S, Sham C, Petrovic V, Voullaire L, Kannourakis G (1995) Cytogenetic and DNA analysis of two neuroectodermal tumors without a simple t(1 1;22). Cancer Genet Cytogenet 83: 12–17.
- Smadja NV, Louvet C, Isnard F, Dutel J-L, Grange M-J, Varette C, Krulik M (1995) Cytogenetic study in multiple myeloma at diagnosis: Comparison of two techniques. Br J Haematol 90: 619–624.
- Sonobe H, Ohtsuki Y, Nakayama H, Asaba K, Nishiya K, Shimizu K (1998) A thymid squamous cell carcinoma with complex chromosome abnormalities. Cancer Genet Cytogenet 103: 83–85.
- Soukup S, Gotwals B, Blough R, Lampkin B (1997) Wilms tumor: Summary of 54 cytogenetic analyses. Cancer Genet Cytogenet 97: 169–171.
- Stark B, Mor C, Jeison M, Gobuzov R, Cohen IJ, Goshen Y, Stein J, Fisher S, Ash S, Yaniv I, Zaizov R (1997) Additional chromosome 1q aberrations and der(16)t(1;16), correlation to the phenotypic expression and clinical behavior of the Ewing family of tumors. J Neuro Oncol 31: 3–8.
- Yamamoto K, Hamaguchi H, Nagata K, Kobayashi M, Tanimoto F, Taniwaki M (1997) Establishment of a novel human acute myeloblastic leukemia cell line (YNH-1) with t(16;21), t(1;16) and 12q 13 translocations. Leukemia 11: 599–608.
