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Article: A comparative study of bone marrow and peripheral blood CD34 + myeloblasts in acute myeloid leukaemia
Title | A comparative study of bone marrow and peripheral blood CD34 + myeloblasts in acute myeloid leukaemia | ||||
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Authors | |||||
Keywords | Acute myeloid leukaemia Bone marrow Engraftment Homing Peripheral blood | ||||
Issue Date | 2009 | ||||
Publisher | Blackwell Publishing Ltd. The Journal's web site is located at http://www.blackwellpublishing.com/journals/BJH | ||||
Citation | British Journal Of Haematology, 2009, v. 144 n. 4, p. 484-491 How to Cite? | ||||
Abstract | To examine the differences between primitive bone marrow (BM) and peripheral blood (PB) myeloblasts in acute myeloid leukaemia (AML), we compared CD34 + myeloblasts of paired BM and PB samples from 14 AML patients in terms of surface phenotype, homing and engraftment in a xenogeneic transplantation model, and gene expression, based on microarray studies and quantitative polymerase chain reaction. While there was no significant difference in surface phenotypes between these two populations, in vivo assay showed significantly better homing potential of PB CD34 + cells than BM CD34 + cells. Significant correlation between homing and engraftment in AML samples was also noted. In addition, gene expression profiling of CD34 + cells from five paired BM and PB leukaemic samples showed that genes involved in G-protein and prostaglandin signalling, chemotaxis and stress response, cell proliferation and apoptosis were down-regulated in PB CD34 + myeloblasts. These data suggested that circulating primitive myeloblasts in AML are functionally different from those residing in the marrow compartment, and such differences may be partly regulated by the BM microenvironment. © 2008 The Authors. | ||||
Persistent Identifier | http://hdl.handle.net/10722/144287 | ||||
ISSN | 2023 Impact Factor: 5.1 2023 SCImago Journal Rankings: 1.574 | ||||
ISI Accession Number ID |
Funding Information: We thank Dr. Agnes SW Chan, Microarray Bioinformatics Specialist of the Genome Centre, University of Hong Kong, for her helpful comments on the data analysis and Prof. Y.L. Kwong, Department of Medicine, University of Hong Kong, for his helpful comments and discussions on the manuscript. We also thank Ms Jenny Chan and Mr. Tsui CO in Department of Medicine, Queen Mary Hospital, for their assistance in sample processing. This work was supported by the University of Hong Kong. | ||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Cheung, AMS | en_HK |
dc.contributor.author | Chow, HCH | en_HK |
dc.contributor.author | Liang, R | en_HK |
dc.contributor.author | Leung, AYH | en_HK |
dc.date.accessioned | 2012-01-20T08:59:47Z | - |
dc.date.available | 2012-01-20T08:59:47Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | British Journal Of Haematology, 2009, v. 144 n. 4, p. 484-491 | en_HK |
dc.identifier.issn | 0007-1048 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/144287 | - |
dc.description.abstract | To examine the differences between primitive bone marrow (BM) and peripheral blood (PB) myeloblasts in acute myeloid leukaemia (AML), we compared CD34 + myeloblasts of paired BM and PB samples from 14 AML patients in terms of surface phenotype, homing and engraftment in a xenogeneic transplantation model, and gene expression, based on microarray studies and quantitative polymerase chain reaction. While there was no significant difference in surface phenotypes between these two populations, in vivo assay showed significantly better homing potential of PB CD34 + cells than BM CD34 + cells. Significant correlation between homing and engraftment in AML samples was also noted. In addition, gene expression profiling of CD34 + cells from five paired BM and PB leukaemic samples showed that genes involved in G-protein and prostaglandin signalling, chemotaxis and stress response, cell proliferation and apoptosis were down-regulated in PB CD34 + myeloblasts. These data suggested that circulating primitive myeloblasts in AML are functionally different from those residing in the marrow compartment, and such differences may be partly regulated by the BM microenvironment. © 2008 The Authors. | en_HK |
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_HK |
dc.relation.ispartof | British Journal of Haematology | en_HK |
dc.subject | Acute myeloid leukaemia | - |
dc.subject | Bone marrow | - |
dc.subject | Engraftment | - |
dc.subject | Homing | - |
dc.subject | Peripheral blood | - |
dc.subject.mesh | Adult | en_HK |
dc.subject.mesh | Aged | en_HK |
dc.subject.mesh | Animals | en_HK |
dc.subject.mesh | Antigens, CD34 - analysis | en_HK |
dc.subject.mesh | Antigens, Neoplasm - analysis | en_HK |
dc.subject.mesh | Bone Marrow Cells - physiology | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Gene Expression Profiling - methods | en_HK |
dc.subject.mesh | Graft Survival | en_HK |
dc.subject.mesh | Granulocyte Precursor Cells - physiology | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Immunophenotyping | en_HK |
dc.subject.mesh | Leukemia, Myeloid, Acute - blood - pathology | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Mice | en_HK |
dc.subject.mesh | Mice, SCID | en_HK |
dc.subject.mesh | Middle Aged | en_HK |
dc.subject.mesh | Neoplasm Transplantation | en_HK |
dc.subject.mesh | Prospective Studies | en_HK |
dc.subject.mesh | Reverse Transcriptase Polymerase Chain Reaction - methods | en_HK |
dc.subject.mesh | Transplantation, Heterologous | en_HK |
dc.title | A comparative study of bone marrow and peripheral blood CD34 + myeloblasts in acute myeloid leukaemia | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Cheung, AMS:h9945256@graduate.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 | Liang, R=rp00345 | en_HK |
dc.identifier.authority | Leung, AYH=rp00265 | en_HK |
dc.description.nature | link_to_OA_fulltext | en_US |
dc.identifier.doi | 10.1111/j.1365-2141.2008.07431.x | en_HK |
dc.identifier.pmid | 19055666 | - |
dc.identifier.scopus | eid_2-s2.0-58549088488 | en_HK |
dc.identifier.hkuros | 157063 | - |
dc.identifier.hkuros | 200892 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-58549088488&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 144 | en_HK |
dc.identifier.issue | 4 | en_HK |
dc.identifier.spage | 484 | en_HK |
dc.identifier.epage | 491 | en_HK |
dc.identifier.eissn | 1365-2141 | - |
dc.identifier.isi | WOS:000262635500003 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Cheung, AMS=36985759800 | en_HK |
dc.identifier.scopusauthorid | Chow, HCH=7102303391 | en_HK |
dc.identifier.scopusauthorid | Liang, R=26643224900 | en_HK |
dc.identifier.scopusauthorid | Leung, AYH=7403012668 | en_HK |
dc.identifier.citeulike | 3939570 | - |
dc.identifier.issnl | 0007-1048 | - |