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骨髓增生异常综合征患者骨髓异常克隆细胞起源的初步研究 被引量:5

Primary Study on Origination of Bone Marrow Abnormal Clones in Patients with Myelodysplastic Syndrome
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摘要 本研究旨在探讨骨髓增生异常综合征(MDS)患者骨髓异常克隆细胞的起源,即MDS患者骨髓CD34+CD38-造血干细胞和CD34+CD38+祖细胞中是否存在恶性克隆细胞及其比例。用免疫磁珠分选技术(MACS)分选9例染色体异常的MDS患者(8三体4例,含有8三体的复杂核型1例,5q-2例,含有5q-的复杂核型1例,5q-合并8三体1例)的骨髓单个核细胞(BMMNC)中的CD34+CD38-细胞和CD34+CD38+细胞,分别涂片;然后在上述涂片上通过荧光原位杂交(FISH)方法比较CD34+CD38-和CD34+CD38+两群细胞中异常克隆细胞的百分比。结果发现,这两群细胞均有异常克隆累及,但CD34+CD38-干细胞中异常克隆的比例(41.8±8.4)%低于CD34+CD38+祖细胞(72.4±7.7)%(p<0.001),而在有核细胞检测的异常克隆细胞比例为(70.8±9.2)%。结论:提示MDS患者中5q-和+8异常克隆均可能起源于造血干细胞阶段,而在祖细胞阶段异常克隆占优势。 The study was aimed to investigate the origination of abnormal clones in hematopoietic cells of MDS patients. That is to say if there are abnormal clones in CD34 + CD38 - and CD34 + CD38 + cells and their proportions in MDS patients. Immuno-magnetic bead technique was used to sort CD34 ~ CD38 - and CD34 + CD38 + in bone marrow mononuclear cells of 9 MDS patients with chromosome abnormalities (four cases with trisomy 8, 1 case with trisomy 8 complex karyotype, 2 cases with 5q-, 1 case with 5q-complex karyotype, 1 case with 5q- accompanying trisomy 8) and smears were made respectively. Then the percentage of abnormal clones in CD34 + CD38 - and CD34 + CD38 + cells were compared by using FISH. The results indicated that abnormal clones were involved in the two population cells in 9 patients. The percentage of abnormal clones in CD34+ CD38 - cells (41.8 ± 8.4% ) was obviously lower than that in CD34+ CD38 + cells ( 72.4 ± 7.7 % ) (p 〈 0.001 ), and the percentage of abnormal clones in karyocytes was 70.8 ± 9. 2%. It is concluded the abnormal clones of bone marrow hematopoietic cells may originate from stem cell stage in MDS patients with 5q- and + 8, and the abnormal clones are predominant at stage of progenitors.
机构地区 苏州大学医学院
出处 《中国实验血液学杂志》 CAS CSCD 2011年第4期930-934,共5页 Journal of Experimental Hematology
关键词 骨髓增生异常综合征 CD34+CD38- CD34+CD38+ 异常克隆 MDS CD34 CD38 abnormal clone
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  • 1Huang WT, Yang X, Zhou X, et al. Multiple distinct clones may co-exist in different lineages in myelodysplastic syndromes. Leuk Res,2009 ;33 (6) :847 - 853. 被引量:1
  • 2Kroef M J, Bolk MJ, Muus P, et al. Mosaicism of the 5 q deletion as assessed by interphase FISH is a common phenomenon in MDS and restricted to mycloid cells. Leukemia, 1997 ; 11 (4) :519 - 523. 被引量:1
  • 3Saitoh K, Miura I, Takahashi N, et al. Fluorescence in situ hybridization of progenitor ceils obtained by fluorescence-activated cell sorting for the detection of cells affected by chromosome abnormality trisomy 8 in patients with myelodysplastic syndromes. Blood, 1998 ;92 ( 8 ) :2886 - 2892. 被引量:1
  • 4Bigoni R, Cuneo A, Milani R, et al. Multilineage involvement in the 5q^- syndrome:a fluorescent in situ hybridization study on bone marrow smears. Haematologica,2001 ;86 (4) :375 - 381. 被引量:1
  • 5Greenberg P. Myelodysplastic syndrome. In: Hoffman R, Benz EJ, Shattil SJ, et al, eds. Hematology, Basic Principles and Practice. Philadelphia, PA: Churchill Livingstone. 2000 : 1106 - 1129. 被引量:1
  • 6Faderl S, Talpaz M, Estrov Z, et al. The biology of chronic myeloid leukemia. N Engl J Med, 1999 ;341 (3) : 164 - 172. 被引量:1
  • 7Heaney ML, Golde DW. Myelodysplasia. N Engl J Med, 1999;340 (21) :1649 - 1660. 被引量:1
  • 8Nilsson L, Astrand-Grundstrom I, Arvidsson I,et al. Isolation and characterization of hematopoietic progenitor/stem cells in 5q^- deleted myelodysplastic syndromes:evidence for involvement at the hematopoietic stem cell level. Blood,2000 ;96 (6) :2012 - 2021. 被引量:1
  • 9Miura I, Kobayashi Y, Takahashi N, et al. Involvement of natural killer ceils in patients with myelodysplastic syndrome carrying monosomy 7 revealed by the application of fluorescence in situ hybridization to cells collected by means of fluorescence-activated cell sorting. Br J Hemato1,2000; 110(4 ) :876 - 879. 被引量:1
  • 10申咏梅,薛永权,李建勇,潘金兰,陈苏宁.骨髓增生异常综合征异常克隆起源的研究[J].中华医学杂志,2002,82(21):1450-1451. 被引量:9

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  • 1马从乾,王雅,赵星,杨轲.肝细胞肝癌中SALL4蛋白表达及其临床病理意义[J].中国老年学杂志,2014,34(10):2714-2715. 被引量:4
  • 2浦杰.骨髓增生异常综合征骨髓活检切片网硬蛋白含量的初步研究[J].华夏医学,2005,18(6):908-909. 被引量:1
  • 3Vardiman JM, Thiele J, Arber DA, et al. The 2008 revision of the WHO classification of myeloid neoplasms and acute leukemia: Rati- onale and important change. Blood, 2009; 114 (5) :937 -951. 被引量:1
  • 4Mufti GJ, Bennett JM, Goasguen J, et al. Diagnosis and classifica- tion of myelodysplastie syndrome: International Working Group on Morphology of myelodysplastie syndrome (IWGM-MDS) consensus proposals for the definition and enumeration of myeloblasts and ring sideroblasts. Haematologica, 2008 ; 93 ( 11 ) : 1712 - 1717,. 被引量:1
  • 5CANTfi RAJNOLDI A, FENU S, KERNDRUP G, et al. Evaluation of dysplastic features in myelodysplastic syndromes : experience from the morphology group of the European Working Group of MDS in Childhood (EWOG-MDS). Ann Hematol, 2005 : 84 (7) : 429 - 433. 被引量:1
  • 6Lipshitz J, Limaye S, Patel D. Leukocyte alkaline phosphatase score correlation with bone marrow blast percentage in myelodysplastic syn- drome. Acta Haematol, 2010; 124(3) :179 - 181. 被引量:1
  • 7Yoshida Y, Katsurada T, Oguma S, et al. Absent or extremely low neutrophil alkaline phosphatase activity levels in patients with myelo- dysplastic syndromes. Intern Med, 2013 ; 52(4) :479 -482. 被引量:1
  • 8A1 - Baradie R, Yamada K, St Hilaire C, et al. Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from muta- tions in SALL4, a new member of the SAL family [ J ]. American journal of human genetics ,2002,71 : 1195 - 1199. 被引量:1
  • 9Cao D, Li J, Guo CC, et al. SALL4 is a novel diagnostic marker for testicular germ cell tumors [ J ]. Am J Surg Patho1,2009,33 (7) :1065 - 1077. 被引量:1
  • 10Ushiku T, Shinozaki A, Shibahara J, et al. SALL4 represents fetal gut differentiation of gastric cancer , and is diagnostically useful in dis- tinguishing hepatoid gastric carcinoma from he patocellular carcinoma [J]. Am J Surg Pat hol,2010,34(4) :533 -540. 被引量:1

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