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Unravelling the relevance of CLEC12A as a cancer stem cell marker in myelodysplastic syndrome
Author(s) -
ToftPetersen Marie,
Nederby Line,
Kjeldsen Eigil,
Kerndrup Gitte B.,
Brown Gordon D.,
Hokland Peter,
Stidsholt Roug Anne
Publication year - 2016
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/bjh.14270
Subject(s) - stem cell , immunophenotyping , cd34 , myelodysplastic syndromes , cancer stem cell , haematopoiesis , cd38 , stem cell marker , cancer research , biology , myeloid , leukemia , immunology , medicine , bone marrow , flow cytometry , microbiology and biotechnology
Summary Evidence of distinct disease propagating stem cells in myelodysplastic syndrome ( MDS ) has emerged in recent years. However, immunophenotypic characterization of these cancer stem cells remains sparse. In acute myeloid leukaemia ( AML ), we have previously described aberrant expression of the C‐type lectin domain family 12, member A ( CLEC 12A) as a stable and reliable marker of leukaemia blasts and as a tool for assessing minimal residual disease. Furthermore, CLEC 12A has been proposed as a promising marker of leukaemic stem cells in AML . The role of CLEC 12A in MDS , however, remains to be elucidated. In this study, we found CLEC 12A aberrantly expressed on the CD 34 + CD 38 − cell compartment in 71% (22/31) of MDS patients, distributed across all Revised International Prognostic Scoring System risk groups. We showed that the CD 34 + CD 38 − CLEC 12A + cells were indeed malignant and possessed functional stem cell properties in the long‐term colony‐initiating cell assay. As opposed to reported findings in AML , we showed that cancer stem cells from MDS samples derived from both CLEC 12A positive and negative CD 34 + CD 38 − subpopulations. Due to the absence of CLEC 12A on normal haematopoietic stem cells, CLEC 12A stem cell immunophenotyping may contribute to diagnosing and monitoring MDS patients and could furthermore add knowledge about disease propagating cells in MDS .