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- Publisher Website: 10.1007/s00277-004-0843-1
- Scopus: eid_2-s2.0-4344623279
- PMID: 14762685
- WOS: WOS:000222691700007
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Article: Epigenetic dysregulation of the Jak/STAT pathway by frequent aberrant methylation of SHP1 but not SOCS1 in acute leukaemias
Title | Epigenetic dysregulation of the Jak/STAT pathway by frequent aberrant methylation of SHP1 but not SOCS1 in acute leukaemias |
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Authors | |
Keywords | Acute leukaemias Jak/STAT Methylation SHP1 SOCS1 |
Issue Date | 2004 |
Publisher | Springer Verlag. The Journal's web site is located at http://link.springer.de/link/service/journals/00277/index.htm |
Citation | Annals Of Hematology, 2004, v. 83 n. 8, p. 527-532 How to Cite? |
Abstract | SOCS1 and SHP1 are negative regulators of the Jak/STAT signalling pathway that is implicated in leukaemogenesis. We studied if aberrant methylation of SOCS1 and SHP1 might be involved in the pathogenesis and prognostication of acute leukaemias by methylation-specific polymerase chain reaction (MSP). At diagnosis, methylation of SHP1 occurred more frequently in acute myeloid leukaemia (AML) (n=26, 52%) than acute lymphoblastic leukaemia (ALL) (n=6, 24%) (p=0.02). Methylation of SOCS1 was absent in both AML and ALL patients. SHP1 methylation was not associated with specific clinicopathologic features and had no prognostic impact on AML patients. Frequent methylation of SHP1, but not SOCS1, may be important in the pathogenesis, but not prognosis, of acute leukaemias. © Springer-Verlag 2004. |
Persistent Identifier | http://hdl.handle.net/10722/78051 |
ISSN | 2023 Impact Factor: 3.0 2023 SCImago Journal Rankings: 0.912 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Chim, CS | en_HK |
dc.contributor.author | Wong, ASY | en_HK |
dc.contributor.author | Kwong, YL | en_HK |
dc.date.accessioned | 2010-09-06T07:38:37Z | - |
dc.date.available | 2010-09-06T07:38:37Z | - |
dc.date.issued | 2004 | en_HK |
dc.identifier.citation | Annals Of Hematology, 2004, v. 83 n. 8, p. 527-532 | en_HK |
dc.identifier.issn | 0939-5555 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/78051 | - |
dc.description.abstract | SOCS1 and SHP1 are negative regulators of the Jak/STAT signalling pathway that is implicated in leukaemogenesis. We studied if aberrant methylation of SOCS1 and SHP1 might be involved in the pathogenesis and prognostication of acute leukaemias by methylation-specific polymerase chain reaction (MSP). At diagnosis, methylation of SHP1 occurred more frequently in acute myeloid leukaemia (AML) (n=26, 52%) than acute lymphoblastic leukaemia (ALL) (n=6, 24%) (p=0.02). Methylation of SOCS1 was absent in both AML and ALL patients. SHP1 methylation was not associated with specific clinicopathologic features and had no prognostic impact on AML patients. Frequent methylation of SHP1, but not SOCS1, may be important in the pathogenesis, but not prognosis, of acute leukaemias. © Springer-Verlag 2004. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Springer Verlag. The Journal's web site is located at http://link.springer.de/link/service/journals/00277/index.htm | en_HK |
dc.relation.ispartof | Annals of Hematology | en_HK |
dc.subject | Acute leukaemias | - |
dc.subject | Jak/STAT | - |
dc.subject | Methylation | - |
dc.subject | SHP1 | - |
dc.subject | SOCS1 | - |
dc.subject.mesh | Acute Disease | en_HK |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Aged | en_HK |
dc.subject.mesh | Aged, 80 and over | en_HK |
dc.subject.mesh | Carrier Proteins - metabolism | en_HK |
dc.subject.mesh | Case-Control Studies | en_HK |
dc.subject.mesh | DNA Methylation | en_HK |
dc.subject.mesh | DNA-Binding Proteins - metabolism | en_HK |
dc.subject.mesh | Epigenesis, Genetic | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Intracellular Signaling Peptides and Proteins | en_HK |
dc.subject.mesh | Janus Kinase 1 | en_HK |
dc.subject.mesh | Leukemia - etiology - metabolism | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Methylation | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Prognosis | en_HK |
dc.subject.mesh | Protein Tyrosine Phosphatase, Non-Receptor Type 6 | en_HK |
dc.subject.mesh | Protein Tyrosine Phosphatases - metabolism | en_HK |
dc.subject.mesh | Protein-Tyrosine Kinases - metabolism | en_HK |
dc.subject.mesh | Repressor Proteins - metabolism | en_HK |
dc.subject.mesh | STAT1 Transcription Factor | en_HK |
dc.subject.mesh | Signal Transduction - genetics | en_HK |
dc.subject.mesh | Suppressor of Cytokine Signaling Proteins | en_HK |
dc.subject.mesh | Trans-Activators - metabolism | en_HK |
dc.title | Epigenetic dysregulation of the Jak/STAT pathway by frequent aberrant methylation of SHP1 but not SOCS1 in acute leukaemias | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0939-5555&volume=83&issue=8&spage=527&epage=32&date=2004&atitle=Epigenetic+dysregulation+of+the+Jak/STAT+pathway+by+frequent+aberrant+methylation+of+SHP1+but+not+SOCS1+in+acute+leukaemias | en_HK |
dc.identifier.email | Chim, CS:jcschim@hku.hk | en_HK |
dc.identifier.email | Kwong, YL:ylkwong@hku.hk | en_HK |
dc.identifier.authority | Chim, CS=rp00408 | en_HK |
dc.identifier.authority | Kwong, YL=rp00358 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1007/s00277-004-0843-1 | - |
dc.identifier.pmid | 14762685 | - |
dc.identifier.scopus | eid_2-s2.0-4344623279 | en_HK |
dc.identifier.hkuros | 88705 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-4344623279&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 83 | en_HK |
dc.identifier.issue | 8 | en_HK |
dc.identifier.spage | 527 | en_HK |
dc.identifier.epage | 532 | en_HK |
dc.identifier.isi | WOS:000222691700007 | - |
dc.publisher.place | Germany | en_HK |
dc.identifier.scopusauthorid | Chim, CS=7004597253 | en_HK |
dc.identifier.scopusauthorid | Wong, ASY=7403144356 | en_HK |
dc.identifier.scopusauthorid | Kwong, YL=7102818954 | en_HK |
dc.identifier.issnl | 0939-5555 | - |