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Article: Differential NOD/SCID mouse engraftment of peripheral blood CD34 + cells and JAK2V617F clones from patients with myeloproliferative neoplasms
Title | Differential NOD/SCID mouse engraftment of peripheral blood CD34 + cells and JAK2V617F clones from patients with myeloproliferative neoplasms | ||||||||
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Authors | |||||||||
Keywords | JAK2 Myeloproliferative disease NOD/SCID mice Polycythemia vera | ||||||||
Issue Date | 2010 | ||||||||
Publisher | Pergamon. The Journal's web site is located at http://www.elsevier.com/locate/leukres | ||||||||
Citation | Leukemia Research, 2010, v. 34 n. 10, p. 1390-1394 How to Cite? | ||||||||
Abstract | We evaluated the NOD/SCID engraftment of CD34 + cells from polycythemia vera (PV) and secondary polycythemia patients (SP) and the JAK2V617F clone before and after transplantation. Peripheral blood CD34 + cells were transplanted intra-femorally. In the injected BM, successful engraftment (>0.1%) occurred in 8/26 mice transplanted with CD34+ cells from 5/13 PV patients (median: 4.26%, range: 0.3-5.56%), in contrast to 0/14 mice from 9 SP patients (P=0.017). The engrafting PV cells were of multi-lineage. JAK2V617F/total JAK2 ratios decreased after transplantation (initial: 65.9% versus 6-week: 13.0%, P=0.001). Essential thrombocythemia (ET) BM cells also exhibited a similar decrease in JAK2V617F clone. The results suggested that events in addition to JAK2V617F are involved in the pathogenesis of PV and ET. © 2010 Elsevier Ltd. | ||||||||
Persistent Identifier | http://hdl.handle.net/10722/123827 | ||||||||
ISSN | 2023 Impact Factor: 2.1 2023 SCImago Journal Rankings: 0.694 | ||||||||
ISI Accession Number ID |
Funding Information: This work was supported by RGC grant (HKU 7488/04M and 7520/06M), a small project funding from CRCG (HKU) and a grant from the Strategic Research Theme on Cancer Stem Cells from HKU. We were grateful to Dr. Harold K.K. Lee, Associate Consultant and the Haematology Team, Princess Margaret Hospital, Hong Kong, for providing us with the venesection samples from some patients. | ||||||||
References | |||||||||
Grants |
DC Field | Value | Language |
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dc.contributor.author | Fung, TK | en_HK |
dc.contributor.author | Cheung, AMS | en_HK |
dc.contributor.author | Kwong, YL | en_HK |
dc.contributor.author | Liang, R | en_HK |
dc.contributor.author | Leung, AYH | en_HK |
dc.date.accessioned | 2010-09-29T06:14:01Z | - |
dc.date.available | 2010-09-29T06:14:01Z | - |
dc.date.issued | 2010 | en_HK |
dc.identifier.citation | Leukemia Research, 2010, v. 34 n. 10, p. 1390-1394 | en_HK |
dc.identifier.issn | 0145-2126 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/123827 | - |
dc.description.abstract | We evaluated the NOD/SCID engraftment of CD34 + cells from polycythemia vera (PV) and secondary polycythemia patients (SP) and the JAK2V617F clone before and after transplantation. Peripheral blood CD34 + cells were transplanted intra-femorally. In the injected BM, successful engraftment (>0.1%) occurred in 8/26 mice transplanted with CD34+ cells from 5/13 PV patients (median: 4.26%, range: 0.3-5.56%), in contrast to 0/14 mice from 9 SP patients (P=0.017). The engrafting PV cells were of multi-lineage. JAK2V617F/total JAK2 ratios decreased after transplantation (initial: 65.9% versus 6-week: 13.0%, P=0.001). Essential thrombocythemia (ET) BM cells also exhibited a similar decrease in JAK2V617F clone. The results suggested that events in addition to JAK2V617F are involved in the pathogenesis of PV and ET. © 2010 Elsevier Ltd. | en_HK |
dc.language | eng | - |
dc.publisher | Pergamon. The Journal's web site is located at http://www.elsevier.com/locate/leukres | en_HK |
dc.relation.ispartof | Leukemia Research | en_HK |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | JAK2 | en_HK |
dc.subject | Myeloproliferative disease | en_HK |
dc.subject | NOD/SCID mice | en_HK |
dc.subject | Polycythemia vera | en_HK |
dc.title | Differential NOD/SCID mouse engraftment of peripheral blood CD34 + cells and JAK2V617F clones from patients with myeloproliferative neoplasms | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0145-2126&volume=34&issue=10&spage=1390&epage=1394&date=2010&atitle=Differential+NOD/SCID+mouse+engraftment+of+peripheral+blood+CD34(+)+cells+and+JAK2V617F+clones+from+patients+with+myeloproliferative+neoplasms | - |
dc.identifier.email | Cheung, AMS:h9945256@graduate.hku.hk | en_HK |
dc.identifier.email | Kwong, YL:ylkwong@hku.hk | en_HK |
dc.identifier.email | Liang, R:rliang@hku.hk | en_HK |
dc.identifier.email | Leung, AYH:ayhleung@hku.hk | en_HK |
dc.identifier.authority | Cheung, AMS=rp01572 | en_HK |
dc.identifier.authority | Kwong, YL=rp00358 | en_HK |
dc.identifier.authority | Liang, R=rp00345 | en_HK |
dc.identifier.authority | Leung, AYH=rp00265 | en_HK |
dc.description.nature | postprint | - |
dc.identifier.doi | 10.1016/j.leukres.2010.01.028 | en_HK |
dc.identifier.pmid | 20170959 | - |
dc.identifier.scopus | eid_2-s2.0-77955984222 | en_HK |
dc.identifier.hkuros | 173552 | - |
dc.identifier.hkuros | 200896 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-77955984222&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 34 | en_HK |
dc.identifier.issue | 10 | en_HK |
dc.identifier.spage | 1390 | en_HK |
dc.identifier.epage | 1394 | en_HK |
dc.identifier.isi | WOS:000281214700022 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.relation.project | A study of normal and deregulated haematopoiesis in zebrafish, with special reference to the role of BMP signaling in haematopoietic stem cell proliferation | - |
dc.identifier.scopusauthorid | Fung, TK=7102715924 | en_HK |
dc.identifier.scopusauthorid | Cheung, AMS=36985759800 | en_HK |
dc.identifier.scopusauthorid | Kwong, YL=7102818954 | en_HK |
dc.identifier.scopusauthorid | Liang, R=26643224900 | en_HK |
dc.identifier.scopusauthorid | Leung, AYH=7403012668 | en_HK |
dc.identifier.citeulike | 6866170 | - |
dc.identifier.issnl | 0145-2126 | - |