MISC

2000年

Quantitative expression of erythropoietin receptor (EPO-R) on acute leukaemia cells: Relationships between the amount of EPO-R and CD phenotypes, in vitro proliferative response, the amount of other cytokine receptors and clinical prognosis

British Journal of Haematology
  • Akihiro Takeshita
  • Kaori Shinjo
  • Masato Higuchi
  • Shuichi Miyawaki
  • Yoshinobu Takemoto
  • Yuji Kishimoto
  • Kenji Saito
  • Hirokuni Takuchi
  • Kazutaka Kuriyama
  • Yukihiko Kimura
  • Norio Asou
  • Masatomo Takahashi
  • Tomomitu Hotta
  • Akihisa Kanamaru
  • Ryuzo Ueda
  • Ryuzo Ohno
  • 全て表示

108
1
開始ページ
55
終了ページ
63
記述言語
英語
掲載種別
DOI
10.1046/j.1365-2141.2000.01828.x

Expression of erythropoietin (EPO) receptor (EPO-R) was analysed in leukaemia cells from 150 patients with acute myeloid leukaemia (AML) or acute lymphoblastic leukaemia (ALL). EPO-R was expressed in 81 (60%) out of 136 AML, and in vitro treatment with EPO led to proliferation of leukaemia cells in 13 (16%) out of 81 AML examined. EPO-R expression and in vitro response to EPO were observed in all subtypes of AML according to the French-American- British (FAB) classification. All eight patients with FAB-M6 expressed EPO-R, and one out of four showed an in vitro response to EPO. Although there was no significant correlation (r=0.2522) between the amount of EPO-R and the in vitro response to EPO, all of the AML patients who showed in vitro response expressed EPO-R. Stem cell factor significantly enhanced both EPO-R expression and in vitro response to EPO. Interleukin-3 tended to increase in vitro response to EPO. CD phenotypes, the amount of granulocyte colony- stimulating factor (G-CSF) receptors and the amount of TPO receptors had no significant relationship with the amount of EPO-R. Patients with both EPO-R expression and in vitro response to EPO had shorter duration of complete remission than those without EPO-R (P=0.0053). EPO-R was expressed in four (29%) out of 14 ALL, and none out of five ALL showed in vitro response to EPO.

リンク情報
DOI
https://doi.org/10.1046/j.1365-2141.2000.01828.x
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/10651724
ID情報
  • DOI : 10.1046/j.1365-2141.2000.01828.x
  • ISSN : 0007-1048
  • PubMed ID : 10651724
  • SCOPUS ID : 0033982421

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