期刊文献+

GRIM-19的表达与膀胱癌组织临床特征的相关性研究 被引量:2

Correlation of GRIM-19 expression and clinical features of bladder cancer
下载PDF
导出
摘要 目的:探讨细胞GRIM-19在膀胱癌组织中的表达及与病理分级和临床分期之间的关系。方法:采用Westernblot方法分别检测50例膀胱癌患者膀胱癌组织、癌旁组织及38例正常膀胱组织中GRIM-19的表达情况,进行分析上述指标与膀胱癌病理分级和临床分期的关系。结果:显示GRIM-19膀胱癌、癌旁组织中的表达与正常膀胱组织比较,差异有统计学意义(P<0.01),膀胱癌、癌旁组织中的表达比较,差异具有统计学意义(P<0.05)。膀胱癌、癌旁组织中的表达:临床分级,Ⅰ级逐渐向Ⅲ级下降,差异具有统计学意义(P<0.01);临床分期,T2~T4高于Tis~T1,差异具有统计学意义(P<0.01);是否转移,转移比未转移的表达量低,差异具有统计学意义(P<0.01)。GRIM-19蛋白在病理分级、临床分期及中是否转移的表达情况,均呈正相关。结论:GRIM-19可以作为判定膀胱癌的预后的一个标准。 Objective:To investigate the relationship of the cells Grim-19expression with pathological grade and clinical stage of bladder cancer.Methods:Western blot methods were used to detect the expression of GRIM-19in cancer tissues and para-carcinoma tissue of 50patients with bladder cancer and normal tissues of 38cases.The relationship of these indicators with bladder cancer pathological grade and clinical stage was analyzed.Results:There was significant difference in GRIM-19expression among cancer tissue,para-carcinoma tissue and normal bladder tissue difference(P0.01),the difference was also significant between cancer tissue and para-carcinoma tissue(P0.05).The expression was significantly decreased as declining clinical stage(P0.01);expression at clinical stage T2to T4was significantly higher than it at Tis-T1(P0.01);the expression was significantly lower in cases with metastasis(P0.01).GRIM-19protein expression was positively correlated with pathological grade,clinical stage and metastasis.Conclusion:GRIM-19can be used as an indicator for determination of bladder cancer prognosis.
出处 《海南医学院学报》 CAS 2013年第10期1372-1374,共3页 Journal of Hainan Medical University
基金 海南省科技厅(811210)~~
关键词 膀胱癌 GRIM-19基因 病理分级 临床分期 Bladder cancer GRIM-19gene Grade Clinical stage
  • 相关文献

参考文献14

  • 1周颖,凌斌.GRIM-19的功能及与肿瘤的相关性[J].医学分子生物学杂志,2008,5(3):262-264. 被引量:30
  • 2Kalvakolanu DV.The GRIMs:a new interface betweencell death regulation and interferon/retinoid inducedgrowth suppression[J].Cytokine Growth Factor Rev,2004,15(2-3):169-194.
  • 3Chidambaram NV,Angell JE,Ling W,et al.Chromo-somal localization of human GRIM-19,a novel IFN-betaand retinoic acid-activated regulator of cell death[J].JInterferon Cytokine Res,2000,20(7):661-665.
  • 4叶静,赵继京,刘荣玉,肖卫华.GRIM-19及其靶基因产物STAT3与肺癌相关性的研究[J].安徽医科大学学报,2008,43(6):599-602. 被引量:11
  • 5张照果,李静,刘岩,李道磊,于世勇,梁晓芳.GRIM-19及其靶基因产物STAT3在胃癌组织中的表达及其意义[J].吉林大学学报(医学版),2011,37(3):499-504. 被引量:8
  • 6Fearnley IM,Carroll J,Shannon RJ,et al.GRIM-19,acell death regulatory gene product,is a subunit ofbovinemitochondrial NADH:ubiquinone oxidoreductase(com-plexI)[J].J Biol Chem,2001,276(42):38345-38348.
  • 7Huang G,Lu H,Hao A,et al.GRIM-19,a cell deathregulatory protein,is essential for assembly and functionof mitochondrial complex I[J].Mol Cell Biol,2004,24:8447-8456.
  • 8Alchanati I,Nallar S C,Sun P,et al.A proteomic analy-sis reveals the loss of expression of the cell death regu-latory gene GRIM-19in human renal cell carcinomas[J].Oncogene,2006,25(54):7138-7147.
  • 9Chen Y,Yuen WH,Fu J,et al.The mitochondrial re-spiratory chain controls intracellular calcium signalingand NFAT activity essential for heart formation in Xe-nopus laevis[J].Mol Cell Biol,2007,27(18):6420-64321.
  • 10Huang G,Chen Y,Lu H,et al.Coupling mitochondrialrespiratory chain to cell death:an essential role of mito-chondrial complex I in the interferon-beta and retinoicacid-induced cancer cell death[J].Cell Death Differ,2007,14(2):327-337.

二级参考文献58

  • 1龚龙波,罗学来,刘双又,陶德定,龚建平,胡俊波.GRIM-19及其靶基因产物STAT3与结直肠癌恶性程度的关系[J].癌症,2007,26(7):683-687. 被引量:43
  • 2Angell J E, Lindner D J, Shapiro P S, et al. Identification of GRIM-19, a novel cell death-regulatory gene induced by the interferon-beta and retinoic acid combination, using a genetic approach [J]. J Biol Chem, 2000, 275 (43) :33416 -26.
  • 3Kalvakolanu D V. The GRIMs : a new interface between cell death regulation and interferon/retinoid induced growth supression [ J ]. Cytokine Growth Factor Rev, 2004, 15 (2-3) : 169 - 94.
  • 4Zhang J, Yang J, Roy S K , et al. The cell death regulator GRIM- 19 is an inhibitor of signal transducer and activator of transcription 3[J]. Proe Natl Acad Sci USA, 2003, 100(16) : 9342-7.
  • 5Lufei C, Ma J, Huang G, et al . GRIM-19, a death-regulatory gene product, suppresses STA33 activity via functional interaction [J]. EMBO J, 2003, 22 (6) :1325 -35.
  • 6Yan X B, Hou H L, Wu L M, et al. Lithium regulates hippocampal neurogenesis by ERK pathway and facilitates recovery of spatial learning and memory in rats after transient global cerebral ischemia[ J]. Neuropharmacology, 2007,53 (4) :487 - 95.
  • 7Lu H, Cao X. GRIM-19 is essential for maintenance of mitochondrial membrane potential[J]. Mol Biol Cell, 2008, 19(5) : 1893 - 902.
  • 8Bromberg J F, Wrzeszczynska M H, Devgan G, et al. Stat3 as an oncogene [ J ]. Cell, 1999, 9S ( 3 ): 295 - 303.
  • 9Bowman T, Garcia R, Turkson J, et al. STATs in oncogenesis [ J ]. Oncogene, 2000, 19 (21 ) : 2474 - 88.
  • 10Mora L B, Buettner R, Seigne J, et al. Constitutive activation of Stat3 in human prostate tumors and cell lines: direct inhibition of Stat3 signaling induces apoptosis of prostate cancer cells [ J ]. Cancer Research, 2002, 62 (22) :6659 - 66.

共引文献69

同被引文献22

  • 1邵月婷,李峰,高丽芳,孙连坤,胡嘉弟,李扬,赵雪俭.人参皂苷Rh_2诱导PC-3M细胞凋亡及其对新基因GRIM-19表达的影响[J].吉林大学学报(医学版),2006,32(2):186-188. 被引量:8
  • 2邵月婷,高丽芳,孙连坤,赵丹,计国义,胡嘉弟,李扬,赵雪俭.ATRA联合IFN-α对PC-3细胞株的生长抑制作用以及对GRIM-19和STAT3基因表达的影响[J].肿瘤,2006,26(3):228-231. 被引量:7
  • 3Perlis N, Zlotta AR, Beyene J, et al. Immediate post-tran- surethral resection of bladder tumor intravesical chemo- therapy prevents non-muscle-invasive bladder cancer re- currences:an updated meta-analysis on 2548 patients and quality-o~evidence review[J]. Eur Urol, 2013,64(3) :421-430.
  • 4Jawa RS, Quist E, Boyer CW, et al. Mesenteric ischemia- reperfusion injury up-regulates certain CC, CXC, and XC ehemokines and results in multi-organ injury in a time-de- pendent mannerEJ]. Eur Cytokine Netw, 2014,24 (4) : 148-156.
  • 5Bernat V, Heinrieh MR, Baumeister P, et al. Synthesis and application of the first radioligand targeting the allosteric binding pocket of chemokine receptor CXCR3 [J ]. ChemMedChem,2012,7(8) ~ 1481-1489.
  • 6Singh AK, Arya RK,Trivedi AK, et al. Chemokine recep- tor trio: CXCR3, CXCR4 and CXCR7 crosstalk via CX- CL11 and CXCL12 [J]. Cytokine Growth Factor Rev, 2013,24(1) ~ 41-49.
  • 7Murakami T, Kawada K, Iwamoto M, et al. The role of CXCR3 and CXCR4 in colorectal cancer metastasis[J]. Int J Cancer,2013,132(2) :276-287.
  • 8Bedognetti D, Spivey TL, Zhao Y, et al. CXCR3/CCR5 path- ways in metastatic melanoma patients treated with adoptive therapy and interleukin-2 [J]. Br J Cancer, 2013, 109 (9) : 2412-2423.
  • 9Hilborn E, Sivik T, Fornander T, et al. C-X-C ligand I0 and C-X-C receptor 3 status can predict tamoxifen treat- ment response in breast cancer patients[J]. Breast Cancer Res Treat,2014,145(1) :73-82.
  • 10Chaturvedi P, Gilkes DM,Wong CC, eta[. Hypoxia-induc- ible factor-dependent breast cancer-mesenchymal stern cell bidirectional signaling promotes metastasis[J]. J Clin In- vest, 2013,123(1) : 189-205.

引证文献2

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部