
TOPK/PBK在儿童恶性淋巴瘤与淋巴结反应性增生的淋巴结组织表达的研究
田鑫, 贺湘玲, 袁小叶, 邹润英, 邹惠, 游亚兰, 陈可可, 朱呈光
中国当代儿科杂志 ›› 2018, Vol. 20 ›› Issue (3) : 214-217.
TOPK/PBK在儿童恶性淋巴瘤与淋巴结反应性增生的淋巴结组织表达的研究
Expression of TOPK/PBK in children with malignant lymphoma or reactive lymphoid hyperplasia
目的 研究TOPK/PBK在恶性淋巴瘤与淋巴结反应性增生患儿淋巴结中的表达差异。方法 以80例恶性淋巴瘤、20例淋巴结反应性增生患儿为研究对象,应用免疫组化检测所有研究对象淋巴结组织的TOPK/PBK表达,对比分析TOPK/PBK的表达情况。结果 恶性淋巴瘤患儿的TOPK/PBK阳性率高于淋巴结反应性增生患儿(P < 0.05);TOPK/PBK阳性率在霍奇金淋巴瘤(HL)与非霍奇金淋巴瘤(NHL)组的差异无统计学意义(P > 0.05);淋巴母细胞淋巴瘤、成熟B细胞淋巴瘤、成熟T/NK细胞淋巴瘤的TOPK/PBK阳性率以淋巴母细胞淋巴瘤最高,但成熟B细胞淋巴瘤与成熟T/NK细胞淋巴瘤的阳性率差异无统计学意义(P > 0.016)。结论 TOPK/PBK在儿童恶性淋巴瘤的淋巴结组织中表达上调,其表达水平可能与NHL病理类型有关。
Objective To study the difference in expression of TOPK/PBK in lymph nodes between children with malignant lymphoma and those with reactive lymphoid hyperplasia. Methods Eighty children with malignant lymphoma and twenty children with reactive lymphoid hyperplasia were enrolled as subjects. Immunohistochemistry was used to determine the expression of TOPK/PBK in all the subjects. The expression of TOPK/PBK was compared between the two groups. Results The TOPK/PBK-positivity rate was significantly higher in children with malignant lymphoma than in those with reactive lymphoid hyperplasia (P < 0.05). There was no significant difference in the TOPK/PBK-positivity rate between the children with Hodgkin's lymphoma and non-Hodgkin's lymphoma (NHL). There were significant differences in the TOPK/PBK-positivity rate among children with different pathological types of NHL (P < 0.05):the children with lymphoblastic lymphoma showed the highest TOPK/PBK-positivity rate and those with mature B-cell lymphoma and mature T/NK-cell lymphoma had a similar TOPK/PBK-positivity rate. Conclusions The expression of TOPK/PBK is up-regulated in the lymph nodes of children with malignant lymphoma. The expression level of TOPK/PBK may be related to the pathological type of NHL.
TOPK/PBK / 恶性淋巴瘤 / 淋巴结反应性增生 / 儿童
TOPK/PBK / Malignant lymphoma / Reactive lymphoid hyperplasia / Child
[1] Ramirez-Avila L, Garner OB, Cherry JD. Relative EBV antibody concentrations and cost of standard IVIG and CMV-IVIG for PTLD prophylaxis in solid organ transplant patients[J]. Pediatr Transplant, 2014, 18(6):599-601.
[2] Raab-Traub N. Novel mechanisms of EBV-induced oncogenesis[J]. Curr Opin Virol, 2012, 2(4):453-458.
[3] Hall LD, Eminger LA, Hesterman KS, et al. Epstein-Barr virus:dermatologic associations and implications:part I. Mucocutaneous manifestations of Epstein-Barr virus and nonmalignant disorders[J]. J Am Acad Dermatol, 2015, 72(1):1-19.
[4] Iwakiri D. Mechanisms of Epstein-Barr virus-mediated oncogenesis[J]. Gan To Kagaku Ryoho, 2015, 42(10):1133-1136.
[5] 赖辉红, 马廉. EB病毒相关恶性肿瘤研究进展[J].中国小儿血液与肿瘤杂志, 2013, 18(6):245-249.
[6] Arber DA, Orazi A, Hasserjian R, et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia[J]. Blood, 2016, 127(20):2391-2405.
[7] Vogelstein B, Papadopoulos N, Velculescu VE, et al. Cancer genome landscapes[J]. Science, 2013, 339(6127):1546-1558.
[8] Simons-Evelyn M, Bailey-Dell K, Toretsky JA, et al. PBK/TOPK is a novel mitotic kinase which is upregulated in Burkitt's lymphoma and other highly proliferative malignant cells[J]. Blood Cells Mol Dis, 2001, 27(5):825-829.
[9] Nandi A, Tidwell M, Karp J, et al. Protein expression of PDZ binding kinase is up-regulated in hematologic malignancies and strongly down regulated during terminal differentiation of HL-60 leukemic cells[J]. Blood Cells Mol Dis, 2004, 32(1):240-245.
[10] 刘宇宏, 刘延香, 黄高, 等. B细胞非霍奇金淋巴瘤PBK/TOPK表达与增殖活性的关系[J]. 临床与实验病理学杂志, 2006, 22(5):541-544.
长沙市科技计划项目长财企指[2017]53号(Kq1701055);湖南省教育厅优秀青年项目(17B163)。