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RIP3在淋巴瘤患者病理组织中的表达 被引量:2

The Expression of Receptor Interaction Protein-3 in Lymphoma Patients Pathology Organization
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摘要 目的:探讨RIP3(受体相互作用蛋白-3)在淋巴瘤患者病理组织中是否表达及其亚细胞定位,并初步观察RIP3的表达是否与淋巴瘤病理恶性度相关。方法:(1)利用免疫组化技术检测48例淋巴瘤和非肿瘤侵润淋巴结病理组织中RIP3表达,并观察RIP3亚细胞定位。结果:(1)RIP3在淋巴瘤患者病理组织中均有表达,其亚细胞定位主要在细胞核,在细胞质中相对弱表达。(2)RIP3表达与淋巴瘤病理恶性度可能存在相关性。结论:RIP3在淋巴瘤患者病理组织中存在阳性表达,为研究RIP3是否与淋巴瘤的发病、临床表现和预后相关,提供了新的探索途径。 Objective: To investigate the expression of RIP3 (receptor interaction protein-3) in lymphoma patients pathological tissues and the sub-cellular localization, and to investigate the relationship of the expression of RIP3 and malignant degree of lymphoma. Methods: The RIP3 expression in 48 cases of the lymphoma and non-neoplastic lymph node pathological tissues was detected by immunohistochemmistry, and the sub-cellular localization of RIP3 was observed. Results: 1) There were RIP3 expresses in the lymphoma pathological tissues, which mainly located in nucleus but weekly in cytoplasm. 2) The expression of RIP3 had a relationship with malignant degrees of lymphoma. Conclusion: There was RIP3 expression in lymphoma pathological tissues, which shell new light to the study of mechanism of lymphoma.
出处 《现代生物医学进展》 CAS 2011年第17期3275-3279,3289,共6页 Progress in Modern Biomedicine
关键词 RIP3 淋巴瘤 病理 免疫组化 RIP3 Lymphoma Pathology Immunohistochemmistry
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  • 1邢小红,吴元明,黄高昇.兔抗人Bit1抗血清的制备及其纯化[J].细胞与分子免疫学杂志,2004,20(6):764-764. 被引量:8
  • 2张娜,李勤喜.两株NIH-3T3细胞间的基因表达差异研究[J].厦门大学学报(自然科学版),2005,44(4):569-571. 被引量:1
  • 3谢琳娜,张娜,陈明谅,李勤喜,周化民.抗RIP3抗体的制备及其亚细胞定位[J].细胞与分子免疫学杂志,2006,22(5):660-663. 被引量:4
  • 4Feng S, Yang Y, Mei Y, et al. Cleavage of RIP3 inactivates its caspase-independent apoptosis pathway by removal of kinase domain. Cell Signal, 2007, 19(10): 2056-2067. 被引量:1
  • 5Meylan E, Bums K, Hofmann K, etal. RIP1 is an essential mediator of Toll-like receptor 3-induced NF-kappa B activation. Nat Immunol, 2004, 5(5): 503-507. 被引量:1
  • 6Rebsamen M, Heinz L X, Meylan E, et ol. DAI/ZBP1 recruits RIP1 and RIP3 through R/P homotypic interaction motifs to activate NF-kappaB. EMBO Rep, 2009, 10(8): 916-922. 被引量:1
  • 7Li Q, Li G, Lan X, et al. Receptor interacting protein 3 suppresses vascular smooth muscle cell growth by inhibition of phosphoinositide-3-kinase-Akt axis. J Biol Chem, 2010, 285(13): 9535-9544. 被引量:1
  • 8Newton K, Sun X, Dixit V M. Kinase RIP3 is dispensable for normal NF-kappa Bs, signaling by the B-cell and T-cell receptors, tumor necrosis factor receptor 1, and Toll-like receptors 2 and 4. Mol Cell Biol, 2004, 24(4): 1464-1469. 被引量:1
  • 9Kumar A, Rothman J H. Cell death: hook, line and linker. Curt Biol, 2007, 17(8): R286-289. 被引量:1
  • 10Van Herreweghe F, Festjens N, Declercq W, et al. Tumor necrosis factor-mediated cell death: to break or to burst, that's the question. Cell Mol Life Sci, 2010, 67(10): 1567-1579. 被引量:1

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