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- Publisher Website: 10.1016/S0165-4608(01)00391-0
- Scopus: eid_2-s2.0-0035395724
- PMID: 11454427
- WOS: WOS:000169770900007
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Article: Derivative (1;18)(q10;q10)a recurrent and novel unbalanced translocation involving 1q in myeloid disorders
Title | Derivative (1;18)(q10;q10)a recurrent and novel unbalanced translocation involving 1q in myeloid disorders |
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Authors | |
Issue Date | 2001 |
Publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/cancergene |
Citation | Cancer Genetics And Cytogenetics, 2001, v. 128 n. 1, p. 35-38 How to Cite? |
Abstract | We report two cases of hematological malignancies, comprising a case of myelodysplastic syndrome (MDS) that rapidly evolved into acute myeloid leukemia, and a case of myeloproliferative disorder (MPD), in which der(1;18)(q10;q10) was found as the sole acquired karyotypic abnormality. This observation indicates that the unbalanced translocation is a recurrent aberration in myeloid disorders. To the best of our knowledge, centromeric fusion between long arms of chromosomes 1 and 18, leading to a normal chromosome 18 substituted with a der(1;18) chromosome, is novel and has not been described in cancer. Mechanistically, either trisomy 1q or monosomy 18p that results from the translocation may potentially contribute to leukemogenesis. Finally, chromosomes with large constitutive heterochromatin bands such as chromosome 1 may be at risk of centromeric instability and be predisposed to centromeric fusion with other chromosomes. Copyright © 2001 Elsevier Science Inc. |
Persistent Identifier | http://hdl.handle.net/10722/148253 |
ISSN | 2012 Impact Factor: 1.929 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wan, TSK | en_US |
dc.contributor.author | Ma, SK | en_US |
dc.contributor.author | Au, WY | en_US |
dc.contributor.author | Chan, LC | en_US |
dc.date.accessioned | 2012-05-29T06:11:48Z | - |
dc.date.available | 2012-05-29T06:11:48Z | - |
dc.date.issued | 2001 | en_US |
dc.identifier.citation | Cancer Genetics And Cytogenetics, 2001, v. 128 n. 1, p. 35-38 | en_US |
dc.identifier.issn | 0165-4608 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/148253 | - |
dc.description.abstract | We report two cases of hematological malignancies, comprising a case of myelodysplastic syndrome (MDS) that rapidly evolved into acute myeloid leukemia, and a case of myeloproliferative disorder (MPD), in which der(1;18)(q10;q10) was found as the sole acquired karyotypic abnormality. This observation indicates that the unbalanced translocation is a recurrent aberration in myeloid disorders. To the best of our knowledge, centromeric fusion between long arms of chromosomes 1 and 18, leading to a normal chromosome 18 substituted with a der(1;18) chromosome, is novel and has not been described in cancer. Mechanistically, either trisomy 1q or monosomy 18p that results from the translocation may potentially contribute to leukemogenesis. Finally, chromosomes with large constitutive heterochromatin bands such as chromosome 1 may be at risk of centromeric instability and be predisposed to centromeric fusion with other chromosomes. Copyright © 2001 Elsevier Science Inc. | en_US |
dc.language | eng | en_US |
dc.publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/cancergene | en_US |
dc.relation.ispartof | Cancer Genetics and Cytogenetics | en_US |
dc.subject.mesh | Acute Disease | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Chromosome Aberrations - Genetics | en_US |
dc.subject.mesh | Chromosome Disorders | en_US |
dc.subject.mesh | Chromosomes, Human, Pair 1 - Genetics | en_US |
dc.subject.mesh | Chromosomes, Human, Pair 18 - Genetics | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Hematologic Diseases - Genetics | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | In Situ Hybridization, Fluorescence | en_US |
dc.subject.mesh | Karyotyping | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Myelodysplastic Syndromes - Genetics | en_US |
dc.subject.mesh | Myeloproliferative Disorders - Genetics | en_US |
dc.subject.mesh | Translocation, Genetic | en_US |
dc.title | Derivative (1;18)(q10;q10)a recurrent and novel unbalanced translocation involving 1q in myeloid disorders | en_US |
dc.type | Article | en_US |
dc.identifier.email | Chan, LC:chanlc@hkucc.hku.hk | en_US |
dc.identifier.authority | Chan, LC=rp00373 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/S0165-4608(01)00391-0 | en_US |
dc.identifier.pmid | 11454427 | - |
dc.identifier.scopus | eid_2-s2.0-0035395724 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0035395724&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 128 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.spage | 35 | en_US |
dc.identifier.epage | 38 | en_US |
dc.identifier.isi | WOS:000169770900007 | - |
dc.publisher.place | United States | en_US |
dc.identifier.issnl | 0165-4608 | - |