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抗凋亡蛋白Bcl-2在非霍奇金淋巴瘤中的表达及其临床意义 被引量:1

The study on the expression of apoptosisa - antagonizing Bcl-2 in non-Hodgkin's lymphoma and its clinical significance
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摘要 目的:通过抗凋亡蛋白Bcl-2的检测,观察其在非霍奇金淋巴瘤(NHL)中的表达及临床意义。方法:用免疫组织化学染色的方法,对34例NHL外检石蜡包埋组织切片进行Bcl-2蛋白的检测。结果:(1)低度恶性NHL中Bcl-2表达高于高度恶性组(P<0.005);(2)B细胞性NHL中Bcl-2的表达高于T细胞性NHL(P<0.025);(3)首次化疗缓解组中的Bcl-2表达低于未缓解组(P<0.01);(4)高Bcl-2表达组的生存期与低表达组之间无差异。结论:抗凋亡蛋白Bcl-2的表达与NHL恶性程度及化疗缓解率相关,可能成为NHL预后的判断指标。 Objective: To evaluate the expression of apoptosisa-antagonizing Bcl-2 and its clinical significance in non-Hodgkin's lymphoma (NHL) . Methods: The Bcl-2 protein was measured by immunohistochemistry on paraffin-embedded specimens in 34 cases of NHL. Results: (1) The expression of Bcl-2 in the low grade NHL was significantly higher than that in the high grade NHL(P<0.005) . (2) The expression of Bcl-2 in B cell NHL was higher than that in T cell NHL (P<0.025). (3) The expression of Bcl-2 in remission group was lower than that in the non ?remission group during the first chemotherapeutics. (4) There was no significant difference about survival time between high and low Bcl-2 expression groups. Conclusion: Bcl-2 was positively related with the malignant grade and remission of chemotherapeutics. Maybe it was a marker for the prognosis.
出处 《临床肿瘤学杂志》 CAS 2001年第1期18-20,共3页 Chinese Clinical Oncology
关键词 非霍奇金淋巴瘤 BCL-2蛋白 免疫组织化学 NHL 抗凋亡蛋白 Non-Hodgkin's lymphomas Bcl-2 protein Immunohistochemistry
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参考文献5

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同被引文献8

  • 1尹丽霞,张伟京.B细胞非霍奇金淋巴瘤重要相关基因的研究进展[J].国外医学(药学分册),2006,33(3):174-177. 被引量:3
  • 2蒋会勇,李慧灵,胡海,何滢,赵彤.弥漫性大B细胞淋巴瘤t(14;18)易位及bcl-2基因扩增的检测[J].中华病理学杂志,2007,36(2):84-89. 被引量:28
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  • 6Che T, You Y, Wang D, et al. MALT1/paracaspase is a signaling component downstream of CARMA1 and mediates T cell receptor-induced NF-kappa B activation[ J]. J Biol Chem,2004(16) : 1587 - 1586.
  • 7Shambharkar PB, Blonska M, Pappu BP, et al. Phosphorylation and ubiquitination of the lkappa B kinase complex by two distinct signaling pathways [ J]. EMBO J, 2007(7) : 1794 - 1805.
  • 8Zhou H, Wertz I, O' Rourke K, et al. BcllO activates the NF-Kappa B pathway through ubiquitination [ J ]. Nature, 2004(6970) : 167 - 171.

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