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Clonal Analysis of Granulocyte-Monocyte Colony-Forming Unit Cells with the Human Androgen Receptor Gene in Chronic Myeloid Leukemia

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Abstract

Coexistence of Philadelphia chromosome-negative (Ph-) progenitors with the Ph+ clone in the early chronic phase of chronic myeloid leukemia (CML) has been documented in previous reports. A different evaluation of methods is needed to justify the clonality of the residual Ph- progenitors. Therefore, the X chromosome inactivation patterns in individual granulocyte-monocyte colony-forming unit (CFU-GM) colonies were studied with the clonality assay for the human androgen receptor gene. A prerequisite for this evaluation was the validation of T-lymphocytes and buccal cells as control cells representing the constitutional lyonization. The percentages of polyclonal CFU-GM cells were determined in 9 Ph[su+] women with CML and in 5 healthy women. Results of the clonal analysis of CFU-GM colonies were compared with those from reverse transcriptase-polymerase chain reaction analysis of single colonies forBCR/ABL transcripts. Both methods of CFU-GM cell analysis were in agreement regarding the presence of variable proportions (0%–94%) of normal cells in CML. Our results suggest that (a) T-cells and buccal cells have potential for use as controls for the clonal analysis of CML cases and (b) this method can evaluate the frequency of polyclonal/clonal CFU-GM cells in CML cases and is applicable to the analysis of myeloid clonal disorders that lack specific molecular markers.

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Correspondence to Nora Viniou.

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Akel, S., Mavroyanni, D., Yataganas, X. et al. Clonal Analysis of Granulocyte-Monocyte Colony-Forming Unit Cells with the Human Androgen Receptor Gene in Chronic Myeloid Leukemia. Int J Hematol 77, 476–481 (2003). https://doi.org/10.1007/BF02986616

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  • DOI: https://doi.org/10.1007/BF02986616

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