CD96 expression on leukemia stem cells in 69 children with acute leukemia

WANG Xue-Mei, YAN Mei, LIU Yu, HAILIQIGULI Nu-Er-Mai-Mai-Ti

Chinese Journal of Contemporary Pediatrics ›› 2013, Vol. 15 ›› Issue (8) : 633-637.

PDF(1351 KB)
PDF(1351 KB)
Chinese Journal of Contemporary Pediatrics ›› 2013, Vol. 15 ›› Issue (8) : 633-637. DOI: 10.7499/j.issn.1008-8830.2013.08.008
CLINICAL RESEARCH

CD96 expression on leukemia stem cells in 69 children with acute leukemia

  • WANG Xue-Mei, YAN Mei, LIU Yu, HAILIQIGULI Nu-Er-Mai-Mai-Ti
Author information +
History +

Abstract

OBJECTIVE: To detect the expression of surface molecule CD96 on stem cell (LSC) in children with acute leukemia, and to explore its clinical significance. METHODS: Bone marrow mononuclear cells were isolated in 69 children with newly diagnosed acute leukemia. CD34+CD38-CD123+ LSCs were separated from these cells by flow cytometry (FCM) and then cultured, and CD96 expression on LSCs was detected by FCM. R-banding technique was used to analyze the karyotypes of the 69 children, and the data of their routine blood and immunological tests were collected. RESULTS: CD96 was mainly expressed in children with acute myelogenous leukemia, and expressed to a lesser extent in those with acute lymphoblastic leukemia (P<0.05). The median expression level of CD96 in Uyghur children was 23.4%, versus 21.2% in Han children (P>0.05). The majority of children with CD96-positive children presented poor-prognosis karyotypes. Compared with CD96-negative children, children with CD96-positive children had a significantly lower complete remission rate (P<0.05) and significantly higher infection and relapse rates after chemotherapy (P<0.05).  CONCLUSIONS: Children with acute leukemia who have CD96-positive LSCs have a poor prognosis. CD96 may be a new indicator of prognosis in children with acute leukemia.

Key words

Acute leukemia / Leukemia stem cell / CD96 / Child

Cite this article

Download Citations
WANG Xue-Mei, YAN Mei, LIU Yu, HAILIQIGULI Nu-Er-Mai-Mai-Ti. CD96 expression on leukemia stem cells in 69 children with acute leukemia[J]. Chinese Journal of Contemporary Pediatrics. 2013, 15(8): 633-637 https://doi.org/10.7499/j.issn.1008-8830.2013.08.008

References

[1] Cox CV, Evely RS, Oakhill A, Pamphilon DH, Goulden NJ, Blair A, et al. Characterization of acute lymphoblastic leukemia progenitor cells[J]. Blood, 2004, 104(9): 2919-2925.



[2] 张丽, 梁英民. 白血病干细胞的分子调控[J]. 现代生物医学进展, 2009, 9(10): 1998-2001.



[3] Hosen N, Park CY, Tatsumi N, Oji Y, Suqiyama H, Gramatzki M, et al. CD96 is a leukemic stem cell-specific marker in human acute myeloid leukemia[J]. Proc Natl Acad Sci USA, 2007, 104(26): 11008-11013.



[4] 朱海波, 赵明峰, 李玉明, 谢芳, 江燕, 徐新女, 等. 白血病干细胞免疫表型与急性白血病疗效及预后的关系[J]. 中华血液学杂志, 2012, 33(1): 58-60.



[5] 中华医学会儿科学分会血液学组, 中华儿科杂志编委会. 小儿急性髓细胞白血病诊疗建议(讨论稿). 2004年全国小儿血液病学术会议, 2004,230-233.



[6] 中华医学会儿科学分会血液学组、中华儿科杂志编委会. 儿童急性淋巴细胞白血病诊疗建议(第三次修订草案)[J]. 中华儿科科杂志, 2006, 44(5): 392-395.



[7] 全国白血病防治研究协作会. 全国白血病防治研究协作会议情况[J]. 医学研究杂志, 1979, 1: 30-35.



[8] Kaspers GJ, Zwaan CM. Pediatric acute myeloid leukemia: towards high-quality cure all patients[J]. Haematologica, 2007, 92(11): 1519-1523.



[9] Maloney K, McGavran L, Murphy J, Odom L, Stork L, Wei Q, et al. TEL-AMLl fusin identifieds a subset of children with standard fist acute lymphoblastic leukemia who have an excdlent prognosis when treated with therapy that includes a single delayed intensification[J]. Leukemia, 1999, 13(11): 1708-1772.



[10] Ramakers-van Woerden NL, Pieters R, Loonen AH, Hubeek I, van Drunen E, Beverloo HB, et al. TEL/AML-l gene fusion is related to in vitro drug sensitivity for L-asparaginase in childhood acute lymphoblastic leukemia[J]. Blood, 2000, 96(3): 1094-1099.



[11] Byrd JC, Dodge RK, Carroll A, Baer MR, Edwards C, Stamberg J, et al. Patients with t(8;21) (q22;q22) and acute myeloid leukemia have superior failure free and over all survival when repetitive cycles of high-dose cytarabine are admin istered[J]. Clin Oncol, 1999, 17(12): 3767-3775.



[12] 何军, 薛永权, 何亚香, 何海龙, 周剑彪, 黄益萍, 等. 160例急性淋巴细胞白血病MICM分型及其治疗和预后相关性的研究[J]. 中华儿科杂志, 2002, 40(3): 152-156.



[13] Aricò M, Valsecchi MG, Camitta B, Schrappe M, Chessells J, Baruchel A, et al. Outcome of treatment in children with Philadelphia chromosome-positive acute lymphoblastic leukemia[J]. N Engl J Med, 2000, 342(14): 998-1006.



[14] Pui CH, Carroll AJ, Raimondi SC, Land VJ, Crist WM, Shuster JJ, et al. Clinical presentation,karyotypic characterization,and treatment outcome of childhood acutelymphoblastic leukemia with a near-haploid or hypodiploid less than45 line[J]. Blood, 1990, 75(5): 1170-1177.



[15] Lapidot T, Sirard C, Vormoor J, Murdoch B, Hoanq T, Caceres-Cortes J, etal. A cell initiating human acute myeloid leukemia after transplantation into SCID mice[J]. Nature, 1994, 367(6464): 645-648.



[16] O’Brien CA, Kreso A, Jamieson CH. Cancer stem cells and self-renewal[J]. Clin Cancer Res, 2010, 16(12): 3113-3120.



[17] Quintana E, Shackleton M, Sabel MS, Fullen DR, Johnson TM, Morrison SJ. Efficient tumour formation by single human melanoma cells[J]. Nature, 2008, 456(7222): 593-598.



[18] Quintana E, Shackleton M, Foster HR, Fullen DR, Sabel MS, Johnson TM, et al. Phenotypic heterogeneity among tumorigenic melanoma cells from patients that is reversible and not hierarchically organized[J]. Cancer Cell, 2010, 18(5): 510-512.



[19] Seth S, Maier MK, Qiu Q, Ravens I, Kremmer E, Forster R, et al. The murine pan T cell marker CD96 is an adhesion receptor for CD155 and nectin-1[J]. Biochem Biophys Res Commun, 2007, 364(4): 959-965.



[20] Lock RB, Jin L, Lee EM. CD123 (IL-3 Receptor Chain) neutralization by a monoclonal antibody selectivelyeliminates human acutemyeloid leukemic stem cells [J]. Blood, 2007, 110: 161.



[21] Hamann PR, Hinman LM, Hollander I, Beyer CF, Lindh D, Holcomb R, et al. Gemtuzumab ozogamicin, a potent and selective anti-CD33 antibody-calicheamicin conjugate for treatment of acute myeloid leukemia[J]. Bioconjug Chem, 2002, 13(1): 47-58.



[22] Fuchs A, Cella M, Giurisato E, Shaw AS, Colonna M. Cutting edge: CD96 (tactile) promotes NK cell target cell adhesion by interacting with the poliovirus receptor (CD155)[J]. J Immunol, 2004, 172(7): 3994-3998.

PDF(1351 KB)

Accesses

Citation

Detail

Sections
Recommended

/