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弥漫大B细胞淋巴瘤中HK-II、TNFAIP3异常表达与肿瘤细胞恶性特征的相关性 被引量:4

Correlation between abnormal expression of HK-Ⅱ and TNFAIP3 and malignancy in diffuse large B-cell lymphoma
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摘要 目的:研究弥漫大B细胞淋巴瘤(DLBCL)中己糖激酶-Ⅱ(HK-Ⅱ)、肿瘤坏死因子α诱导蛋白3基因(TNFAIP3)异常表达与肿瘤细胞恶性特征的相关性。方法:选择2016年3月~2018年3月期间在我院手术切除的DLBCL患者作为DLBCL组,同期手术切除且经病理证实为淋巴结反应性增生的患者作为对照组,收集病灶后测定HK-Ⅱ、TNFAIP3、增殖基因、侵袭基因的表达量。结果:DLBCL组患者病灶内HK-Ⅱ的mRNA表达量明显高于对照组,TNFAIP3的mRNA表达量明显低于对照组;DLBCL组淋巴瘤分期Ⅲ~Ⅳ期、淋巴瘤分组B组患者病灶内HK-Ⅱ的mRNA表达量明显高于I~Ⅱ期患者、A组患者,TNFAIP3的mRNA表达量明显低于I~Ⅱ期患者、A组患者;DLBCL组患者病灶内CyclinD2、PDE4B、BCL2、XIAP、CCL5、CXCR4、MMP26的mRNA表达量明显高于对照组且与HK-II呈正相关、与TNFAIP3呈负相关,Caspase-3、TIMP4的mRNA表达量明显低于对照组且与HK-Ⅱ呈负相关、与TNFAIP3呈正相关。结论:DLBCL中HK-Ⅱ的高表达以及TNFAIP3的低表达与肿瘤病理进程、肿瘤细胞增殖及侵袭密切相关。 Objective: To study the correlation of the abnormal expression of hexokinase-Ⅱ (HK-Ⅱ) and tumor necrosis factor alpha-induced protein 3 (TNFAIP3) and the malignant features of tumor cells in diffuse large B-cell lymphoma (DLBCL). Methods: DLBCL patients who underwent surgical resection in our hospital between March 2016 and March 2018 were selected as the DLBCL group, and the patients who underwent surgical resection and were pathologically confirmed as reactive hyperplasia of lymph nodes during the same period were selected as the control group. The lesions were collected to measure the expression levels of HK-Ⅱ, TNFAIP3, proliferation genes and invasion genes. Results: HK-Ⅱ mRNA expression level in the lesions of the DLBCL group was significantly higher than that of the control group while TNFAIP3 mRNA expression level was significantly lower than that of the control group; In DLBCL group, HK-Ⅱ mRNA expression levels in the lesions of patients with lymphoma stage Ⅲ-Ⅳ and lymphoma group B were significantly higher than those of the patients with lymphoma stage I-Ⅱ and lymphoma group A while TNFAIP3 mRNA expression levels were significantly lower than those of the patients with lymphoma stage I-Ⅱ and lymphoma group A; In the lesions of the DLBCL group, CyclinD2, PDE4B, BCL2, XIAP, CCL5, CXCR4 and MMP26 mRNA expression levels were significantly higher than those of the control group, and were positively correlated with HK-Ⅱ and negatively correlated with TNFAIP3; while Caspase-3 and TIMP4 mRNA expression levels were significantly lower than those of the control group, and were negatively correlated with HK-Ⅱ and positively correlated with TNFAIP3. Conclusions: The high expression of HK-Ⅱ and the low expression of TNFAIP3 in DLBCL are closely related to the pathological process of tumor as well as the proliferation and invasion of tumor cells.
作者 秦英 QIN Ying(Hematology Department,Ya'an People's Hospital in Sichuan Province,Ya'an 625000,China)
出处 《海南医学院学报》 CAS 2018年第22期2015-2018,2022,共5页 Journal of Hainan Medical University
基金 四川省科技攻关计划基金项目(2003sz0398)~~
关键词 弥漫大B细胞淋巴瘤(DLBCL) 己糖激酶-Ⅱ(HK-Ⅱ) 、肿瘤坏死因子α诱导蛋白3基因(TNFAIP3) 增殖 侵袭 Diffuse large B-cell lymphoma Hexokinase-II Tumor necrosis factor alpha-induced protein 3 Proliferation Invasion
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  • 1钟美佐,黄进,翟晓,刘巍,李建璜,陈方平.MMP-9、MMP-2在非霍奇金淋巴瘤病理组织中的表达及意义[J].现代肿瘤医学,2006,14(2):218-220. 被引量:8
  • 2关立华,张淑兰.基质金属蛋白酶-26和金属蛋白酶组织抑制剂-4在子宫内膜癌组织中的表达[J].山西医药杂志,2007,36(2):121-125. 被引量:8
  • 3Menon M P, Pittaluga S, Jaffe E S. The histological and biological spectrum of diffuse large B-cell lymphoma in the WHO classifica- tion[J]. Cancer J, 2012,18(5) :411 -20.
  • 4Hymowitz S G, Wertz I E. A20: from ubiquitin editing to tumour suppression[J]. Nat Rev Cancer, 2010,10(5) :332 -41.
  • 5Chanudet E, Huang Y, Ichimura K, et al. A20 is targeted by pro- rooter methylation, delc-tion and inactivating mutation in MALTlymphoma [ J ]. Leukemia, 2010,24 ( 2 ) :483 - 7.
  • 6Davis R E, Brown K D, Siebenlist U, et al. Constitutive nuclear faetor kappaB activity is required for survival of activated B cell-like diffuse large B cell lymphoma cells[J]. J Exp Med, 2001,194 (12) :1861 -74.
  • 7Kojima K, Fujino Y, Goto-Koshino Y, et al. Analysis on activation of NF-KB and eft~ct of bortezomib in canine neoplastic lymphoid cell lines[J]. J Vet Med Sci, 2013,75(6) :727 -31.
  • 8Opipari A W Jr, Boguski M S, Dixit V M. The A20 cDNA induced by tumor necrosis factor alpha encodes a novel type of zinc finger protein [ J ]. Biol Chem, 1990,265 ( 25 ) : 14705 - 8.
  • 9Vereecke L, Beyaert R, Van Loo G, et al. The ubiquitin-editing enzyme A20 ( TNFAIP3 ) is a central regulator of immunopathology [J]. Trends Immunol, 2009,30 ( 8 ) : 383 - 91.
  • 10Weaver E A, Chen C Y, May S M, et al. Comparison of adenovi- ruses as oncolytics and cancer vaccines in an immunocompetent n cell lymphoma model[ J ]. Hum Gcne Ther, 2011,22 (9) : 1095 - 100.

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