|Table of Contents|

The expression characteristic of inhibitory B7 family molecules in acute myeloid leukemia

Journal Of Modern Oncology[ISSN:1672-4992/CN:61-1415/R]

Issue:
2021 05
Page:
872-877
Research Field:
Publishing date:

Info

Title:
The expression characteristic of inhibitory B7 family molecules in acute myeloid leukemia
Author(s):
ZHANG Lingyi12ZHANG Wei3LIN Jiang2CHEN Qiaoyun2QIAN Jun3YUAN Qian3ZHOU Jingdong3ZHANG Tingjuan13ZHOU Hong1
1.School of Medicine,Jiangsu University,Jiangsu Zhenjiang 212013,China;2.Laboratory Center;3Department of Hematology,the Affiliated People's Hospital of Jiangsu University,Jiangsu Zhenjiang 212002,China.
Keywords:
B7 costimulatory moleculesflow cytometryacute myeloid leukemiamembrane proteinexpression
PACS:
R733.71
DOI:
10.3969/j.issn.1672-4992.2021.05.034
Abstract:
Objective:To investigate the expression and distribution of B7-H1,B7-H3,B7-H4 and B7-H6 in human acute myeloid leukemia (AML).Methods:The membrane protein expression of B7-H1,B7-H3,B7-H4 and B7-H6 in 8 AML cell lines and bone marrow blast cells of 22 de novo AML patients were detected by flow cytometry,with that of 8 volunteers as control.The expression rate of positive cells,mean fluorescence intensity (MFI) and mean fluorescence intensity ratio of blast cells and lymphocytes (MFI ratio) were used to evaluate the expression characteristic of these B7 molecules.Results:Majority of AML cell lines expressed high or detectable level of membrane protein B7-H3 and B7-H6.The expression of B7-H3 was higher in SKM-1 and SHI-1,and B7-H6 had higher expression in K562 and HL-60.B7-H1 was highly expressed only in HEL,while B7-H1 membrane protein was not expressed in other AML cell lines.B7-H4 was undetectable in AML cell lines.The expression rate and MFI ratio of membrane protein B7-H3 and B7-H6 in de novo AML blast cells was significantly higher than that of control.And peripheral white blood cells of group with high B7-H3 expression were significantly higher when compared with group with low B7-H3 expression,and age of the group with high B7-H6 expression was also significantly higher than that of the group with low B7-H6 expression.Expression of B7-H3 and B7-H6 was elevated in patients with acute monocytic leukemia.The expression of B7-H1 and B7-H4 in de novo AML patients was low or undetectable,and there was no significant difference compared with control.Conclusion:There are differences among expression characteristics of four inhibitory B7 family molecules in AML cell lines and patients.The abnormally elevated expression of B7-H3 and B7-H6 in de novo AML suggests that the two B7 family molecules may be involved in occurrence and progression of acute myeloid leukemia.

References:

[1]GREAVES P,GRIBBEN JG.The role of B7 family molecules in hematology malignancy[J].Blood,2013,121(5):734-744.
[2]LING N,CHEN D.New B7 family checkpoints in human cancers[J].Mol Cancer Ther,2017,16(7):1203-1211.
[3]CLARKE BJ,LIAO SK,LEEDS C,et al.Distribution of a hematopoietic-specific differentiation antigen of K562 cells in the human myeloid and lymphoid cell lineages[J].Cancer Res,1987,47(16):4254-4259.
[4]BARBUI T,THIELE J,GISSLINGER H,et al.The 2016 WHO classification and diagnostic criteria for myeloproliferative neoplasms:document summary and in-depth discussion[J].Blood Cancer J,2018,8(2):15.
[5]HARRINGTON AM,OLTEANU H,KROFT SH.A dissection of the CD45/side scatter "blast gate"[J].Am J Clin Pathol,2012,137(5):800-804.
[6]GUERY T,ROUMIER C,BERTHON C,et al.B7-H3 protein expression in acute myeloid leukemia[J].Cancer Medicine,2015,4(12):1879-1883.
[7]HU Y,LV X,WU YJ,et al.Expression of costimulatory molecule B7-H3 and its prognostic implications in human acute leukemia[J].Hematology,2015,20(4):187-195.
[8]ISHIDA M,IWAI Y,TANAKA Y,et al.Different expression of PD-L1 and PD-L2,ligands for an inhibitory receptor PD-1,in cells of lymphohematopoietic tissues[J].Immunol Lett,2002,84(1):57-62.
[9]CHAPOVAL AI,NI J,LAU JS,et al.B7-H3:a costimulatory molecule for T cell activation and IFN-gamma production[J].Nat Immunol,2001,2(3):269-274.
[10]PRASAD DV,RICHARDS S,MAI XM,et al.B7S1,a novel B7 family member that negatively regulates T cell activation[J].Immunity,2003,18(6):863-873.
[11]杨思源,王晶,克晓燕.B7-H6在恶性肿瘤中的研究进展[J].肿瘤研究与临床,2019,31(4):272-275. YANG SY,WANG J,KE XY.Progress of B7-H6 in malignant tumor[J].Cancer Research and Clinic,2019,31(4):272-275.
[12]WU X,GU Z,CHEN Y,et al.Application of PD-1 blockade in cancer immunotherapy[J].Comput Struct Biotechnol J,2019,17:661-674.
[13]YANG H,BUESO-RAMOS C,DINARDO C,et al.Expression of PD-L1,PD-L2,PD-1 and CTLA4 in myelodysplastic syndromes is enhanced by treatment with hypomethylating agents[J].Leukemia,2014,28(6):1280-1288.
[14]ZHANG ZF,ZHANG QT,XING HZ,et al.Expression of programmed death ligand-1(PD-L1) in human acute leukemia and its clinical significance[J].Journal of Experimental Hematology,2015,23(4):930-934.
[15]XIA F,ZHANG Y,XIE L,et al.B7-H4 enhances the differentiation of murine leukemia initiating cells via the PTEN/AKT/RCOR2/RUNX1 pathways[J].Leukemia,2017,31(10):2260-2264.
[16]张巍,王晶,王艳芳,等.共刺激分子B7-H1、B7-H3和B7-H4在血液系统恶性肿瘤细胞株中的表达水平和分布特征[J].中国实验血液学杂志,2016,24(5):1539-1546. ZHANG W,WANG J,WANG YF,et al.Expression and subcellular distribution of costimulatory molecules B7-H1,B7-H3 and B7-H4 in human hematologic malignancy cell lines[J].Journal of Experimental Hematology,2016,24(5):1539-1546.
[17]张巍,林江,陈巧云,等.B7共刺激分子在恶性血液病细胞株中的表达特征[J].江苏大学学报:医学版,2018,28(5):387-392. ZHANG W,LIN J,CHEN QY,et al.The expression characteristic of B7 costimulatory molecules in human hematologic malignancy cell lines[J].Journal of Jiangsu University(Medicine Edition),2018,28(5):387-392.
[18]CAO GS,WANG J,ZHENG XD,et al.Tumor therapeutics work as stress inducers to enhance tumor sensitivity to natural killer (NK) cell cytolysis by up-regulating NKp30 ligand B7-H6[J].Journal of Biological Chemistry,2015,290:29964-29973.
[19]BRANDT CS,BARATIN M,YI EC.The B7 family member B7-H6 is a tumor cell ligand for the activating natural killer cell receptor NKp30 in humans[J].The Journal of Experimental Medicine,2009,206(7):1495-1503.

Memo

Memo:
江苏省基础研究计划青年基金资助项目(编号:BK20180280);镇江市社会发展项目(编号:SH2016045);江苏大学附属人民医院博士启动基金资助项目(编号:KFB201603)
Last Update: 2021-01-29