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B7-H6 mRNA在结肠癌中的表达和临床意义 被引量:2

The expression and clinical significance of B7-H6 mRNA in colon cancer
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摘要 目的探讨B7-H6 mRNA在结肠癌中的表达水平和临床意义。方法以65例结肠癌组织和15例癌旁组织为研究对象,使用q PCR检测B7-H6 mRNA表达水平,并结合临床资料,利用卡方检验分析B7-H6 mRNA表达水平与病理参数的相关性。采用Kaplan-Meier法(生存期分析)比较不同B7-H6 mRNA表达水平和患者预后的关系。结果通过确切概率法发现,不同B7-H6 mRNA表达水平的癌组织具有不同的肿瘤浸润程度,差异具有统计学意义(P=0.042),B7-H6 mRNA高表达组更倾向于外膜外浸润,而低表达组则倾向于深肌层浸润。而不同的B7-H6 mRNA表达水平与其他的病理参数(性别、年龄、肿瘤外形、病理类型、N分期以及临床分期)指标之间则差异无统计学意义(P值均>0.05)。生存期分析发现,与B7-H6 mRNA低表达组相比,B7-H6 mRNA高表达组结肠癌患者预后生存期显著降低,差异具有统计学意义(P=0.008)。结论高表达B7-H6 mRNA的患者的肿瘤更易于浸润到外膜外并累及其他组织器官,且高表达水平的患者更倾向于预后不良。 B7-H6 is a newly discovered member of the B7 family.The expression and clinical significance of B7-H6 mRNA in cancer tissues remains unclear.In this study,we intend to investigate the expression of B7-H6 mRNA in colon cancer by qPCR,and the correlation between the expression level of B7H6 and pathological parameters was analyzed by chi-square test combined with clinical data.Kaplan-Meier method(survival analysis)was used to compare the prognosis of patients with different levels of B7-H6 expression.The exact probability method showed that the cancer tissues with different B7-H6 expression levels had different degrees of invasion(P=0.042).The high expression group of B7-H6 gene tended to infiltrate the outer membrane,while the low expression group tended to infiltrate the deep muscle.However,there was no significant difference in the expression level of B7-H6 gene between different pathological parameters(sex,age,tumor shape,pathological type,N stage and clinical stage)(P>0.05).Survival analysis showed that the prognostic survival time of colon cancer patients with high expression of B7-H6 gene was significantly lower than those with low expression of B7-H6 gene(P=0.008).In conclusion,the tumors of patients with high expression of B7-H6 are more likely to invade the outer membrane and involve other tissues and organs,and patients with high expression of B7-H6 are more likely to have poor prognosis.
作者 吴大广 徐兰 王振欣 张光波 WU Daguang;XU Lan;WANG Zhenxin;ZHANG Guangbo(Department of Oncology,Funing County People’s Hospital,Yancheng 224400,China;Jiangsu Provncial Key Laboratory of Clinical Immunology,Suzhou 215006,China;Department of Oncology,First Affiliated Hospital of Soochow University,Suzhou 215007,China)
出处 《免疫学杂志》 CAS CSCD 北大核心 2019年第10期891-895,共5页 Immunological Journal
基金 苏州市民生科技项目(SS201631)
关键词 结肠癌 B7-H6 MRNA 侵袭转移 生存期 Colon cancer B7-H6 Invasion and metastasis Survival
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  • 1张光波,陈永井,姜智,於葛华,杨明峰,施勤,王勤,李文香,张学光.人B7-H3基因转染及其生物学功能的研究[J].现代免疫学,2004,24(6):455-459. 被引量:9
  • 2[1]Suh WK,Gajewska BU,Okada H,et al.The B7 family member B7-H3 preferentially down-regulates T helper type 1-mediated immune responses[J].Nat Immunol,2003,4(9):899-906.
  • 3[2]Linsley PS,Brady W,Urnes M,et al.CTLA-4 is a second receptor for the B cell activation antigen B7[J].J Exp Med,1991,174(3);561-569.
  • 4[3]Bretscher PA.A two-step,two-signal model for the primary activation of precursor helper T cells[J].Proc Natt Acad Sci USA,1999,96(1):185-190.
  • 5[4]Dong H,Strome SE,Salomao DR,et al.Tumor-associated B7-H1 promotes T-cell apoptosis:a potential mechanism of immune evasion[J].Nat Med,2002,8(8):793-800.
  • 6[5]Curiel TJ,Wei S,Dong H,et al.Blockade of B7-H1 improves myeloid dendritic cell-mediated antitumor immunity[J].Nat Med,2003,9(5):562-567.
  • 7[6]Iwai Y,Ishida M,Tanaka Y,et al.Involvement of PD-L1 on tumor cells in the escape from host immune system and tumor immunotherapy by PD-L1 blockade[J].Proc Natl Acad Sci USA,2002,99(19):12293-12297.
  • 8[7]Yoshinaga SK,Whoriskey JS,Khare SD,Zhang XG,et al.T-cell co-stimulation through B7RP-1 and ICOS[J].Nature,1999,402(6763):827-832.
  • 9[8]Zhang GB,Zhou H,Zhang XG,et al.Characterization and application of two novel monoclonal antibodies against 2IgB7-H3:expression analysis of 2IgB7-H3 on dendritic cells and tumor cells[J].Tissue Antigen,2005,66(2):83-92.
  • 10[9]Zhou ZH,Wang JF,Wang YD,et al.An agonist anti-human CD40 monoclonal antibody that induces dendritic cell formation and maturation and inhibits proliferation of a myeloma cell line[J].Hybridoma,1999,18(6):471-478.

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