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- Publisher Website: 10.1046/j.1365-2141.2002.03952.x
- Scopus: eid_2-s2.0-0036456441
- PMID: 12472578
- WOS: WOS:000179693100017
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Article: Infrequent hypermethylation of CEBPA promotor in acute myeloid leukaemia
Title | Infrequent hypermethylation of CEBPA promotor in acute myeloid leukaemia |
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Authors | |
Keywords | Acute myeloid leukaemia CEBPA Hypermethylation |
Issue Date | 2002 |
Publisher | Blackwell Publishing Ltd. The Journal's web site is located at http://www.blackwellpublishing.com/journals/BJH |
Citation | British Journal Of Haematology, 2002, v. 119 n. 4, p. 988-990 How to Cite? |
Abstract | The gene CEBPA, encoding the transcription factor C/EBPα, is crucial for granulocyte differentiation. We investigated the frequency of aberrant CEBPA promotor methylation with the methylation-specific polymerase chain reaction in 70 patients with acute myeloid leukaemia (AML). Two patients, both with M2 morphology, were found to have methylated CEBPA. In one of them, the fusion gene AML1/ETO, reported to cause transcription repression of CEBPA, was also present, suggesting that more than one mechanism might collaborate to suppress CEBPA gene expression. Aberrant CEBPA methylation is infrequent in AML, but may occur preferentially in the M2 phenotype. |
Persistent Identifier | http://hdl.handle.net/10722/162615 |
ISSN | 2023 Impact Factor: 5.1 2023 SCImago Journal Rankings: 1.574 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Chim, CS | en_US |
dc.contributor.author | Wong, ASY | en_US |
dc.contributor.author | Kwong, YL | en_US |
dc.date.accessioned | 2012-09-05T05:21:42Z | - |
dc.date.available | 2012-09-05T05:21:42Z | - |
dc.date.issued | 2002 | en_US |
dc.identifier.citation | British Journal Of Haematology, 2002, v. 119 n. 4, p. 988-990 | en_US |
dc.identifier.issn | 0007-1048 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/162615 | - |
dc.description.abstract | The gene CEBPA, encoding the transcription factor C/EBPα, is crucial for granulocyte differentiation. We investigated the frequency of aberrant CEBPA promotor methylation with the methylation-specific polymerase chain reaction in 70 patients with acute myeloid leukaemia (AML). Two patients, both with M2 morphology, were found to have methylated CEBPA. In one of them, the fusion gene AML1/ETO, reported to cause transcription repression of CEBPA, was also present, suggesting that more than one mechanism might collaborate to suppress CEBPA gene expression. Aberrant CEBPA methylation is infrequent in AML, but may occur preferentially in the M2 phenotype. | en_US |
dc.language | eng | en_US |
dc.publisher | Blackwell Publishing Ltd. The Journal's web site is located at http://www.blackwellpublishing.com/journals/BJH | en_US |
dc.relation.ispartof | British Journal of Haematology | en_US |
dc.rights | British Journal of Haematology. Copyright © Blackwell Publishing Ltd. | - |
dc.subject | Acute myeloid leukaemia | - |
dc.subject | CEBPA | - |
dc.subject | Hypermethylation | - |
dc.subject.mesh | Acute Disease | en_US |
dc.subject.mesh | Base Sequence | en_US |
dc.subject.mesh | Ccaat-Enhancer-Binding Protein-Alpha - Genetics | en_US |
dc.subject.mesh | Dna Methylation | en_US |
dc.subject.mesh | Dna, Neoplasm - Genetics | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Leukemia, Myeloid - Genetics | en_US |
dc.subject.mesh | Leukemia, Myeloid, Acute - Genetics | en_US |
dc.subject.mesh | Molecular Sequence Data | en_US |
dc.subject.mesh | Neoplasm Proteins - Genetics | en_US |
dc.subject.mesh | Polymerase Chain Reaction - Methods | en_US |
dc.subject.mesh | Promoter Regions, Genetic | en_US |
dc.subject.mesh | Sensitivity And Specificity | en_US |
dc.title | Infrequent hypermethylation of CEBPA promotor in acute myeloid leukaemia | en_US |
dc.type | Article | en_US |
dc.identifier.email | Chim, CS:jcschim@hku.hk | en_US |
dc.identifier.email | Kwong, YL:ylkwong@hku.hk | en_US |
dc.identifier.authority | Chim, CS=rp00408 | en_US |
dc.identifier.authority | Kwong, YL=rp00358 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1046/j.1365-2141.2002.03952.x | en_US |
dc.identifier.pmid | 12472578 | - |
dc.identifier.scopus | eid_2-s2.0-0036456441 | en_US |
dc.identifier.hkuros | 77961 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0036456441&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 119 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.spage | 988 | en_US |
dc.identifier.epage | 990 | en_US |
dc.identifier.isi | WOS:000179693100017 | - |
dc.publisher.place | United Kingdom | en_US |
dc.identifier.scopusauthorid | Chim, CS=7004597253 | en_US |
dc.identifier.scopusauthorid | Wong, ASY=7403144356 | en_US |
dc.identifier.scopusauthorid | Kwong, YL=7102818954 | en_US |
dc.identifier.issnl | 0007-1048 | - |