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Rho家族蛋白在胰腺癌组织中的表达及临床意义 被引量:1

Expression and clinical significance of Rho family proteins in pancreatic cancer
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摘要 目的研究Rho家族中3个重要成员RhoA、RhoB、RhoC在胰腺癌组织中的表达及其临床意义。方法运用免疫组织化学SP法检测43例胰腺癌组织及25例正常胰腺组织中RhoA、RhoB、RhoC蛋白的表达情况,并分析它们的表达与胰腺癌临床病理特征之间的关系。结果 RhoA、RhoC蛋白在胰腺癌组织中的阳性表达率分别为76.7%和72.1%,在正常胰腺组织中的阳性表达率分别为28.0%和20.0%,两者比较差异均有统计学意义(P<0.05);RhoB蛋白在胰腺癌组织中的阳性表达率为4.7%,在正常胰腺组织中的阳性表达率为32.0%,两者比较差异有统计学意义(P<0.05);RhoA、RhoC蛋白表达均与胰腺癌的分化程度、肿瘤分期、有无淋巴结转移密切相关(P<0.05)。结论 RhoA、RhoC蛋白的表达与胰腺癌的发生发展、浸润转移密切相关。 [Objective] To investigate the expression of three important members of Rho family in pan- creatic cancer and their clinical significance. [Methods] The expression of RhoA, RhoB and RhoC was de- tected by immunohistochemistry (SP) method in 43 cases of pancreatic cancer, 25 cases of normal tissues, the relationship between expressions of RhoA and RhoC and clinicopathologieal features were analyzed. [Results] The positive rates of RhoA and RhoC are 76.7%, 72.1% in pancreatic carcinoma, which was significantly higher than those in normal pancreatic tissues (28.0% and 20.0%, respectively) (P〈0.05); The positive rate of RhoB are 4.7% in pancreatic carcinoma, 32.0% in normal pancreatic tissues, There was significant difference (P〈0.05); RhoA and RhoC expression were closely related with pancreatic cancer differentiation degree, TNM staging, lymph node metastasis (P 〈0.05). [ Conclusion] The expression of RhoA and RhoC are closely related to the carcinogenesis, progress, invasion and metastasis of pancreatic carcinoma.
出处 《中国现代医学杂志》 CAS CSCD 北大核心 2014年第2期54-57,共4页 China Journal of Modern Medicine
基金 国家自然科学基金(No:81160311) 贵州省科教青年英才培养工程基金(No:黔省专合字[2012]177号) 贵州省科技厅2011年度社会攻关计划基金(No:黔科合SY字[2011]3007) 贵州省肝胰疾病研究科技创新人才团队基金(No:黔科合人才团队[2010]4010)
关键词 胰腺癌 Rho家族 免疫组织化学 pancreatic cancer Rho family imunohistochemistry
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参考文献11

  • 1MAISONNEUVE P,LOWENFELS AB.Epidemiology of pancreat-ic cancer:an update[J].Dig Dis,2010,28(4-5):645-656.
  • 2WATANABE N,KATO T,FUJITA A,et al.Cooperation betweenmDial and ROCK in Rho-induced actin reorganization[J].NatCell Biol,1999,1(3):136-143.
  • 3SAHAI E,MARSHALL CJ.Rock and Dia have opposing effectson adherens junctions downstream of Rho[J].Nat Cell Biol,2002,4(6):408-415.
  • 4SAHAI E,MARSHALL CJ.Rho-GTPasas and cancer[J].Nat RevCancer,2002,2(2):133-142.
  • 5FRITZ G,JUST I,KAINA B.Rho GTPases are over-expressedin human tumors[J].Int J Cancer,1999,81(5):682-687.
  • 6ABRAHAM MT,KURIAKOSE MA,SACKS PG,et al.Motili-ty-related proteins as markers for head and neck squamous cellcancer[J].Laryngoscope,2001,111(7):1285-1289.
  • 7FARIED A,FARIED LS,KIMURA H,et al. RhoA and RhoCproteins promote both cell proliferation and cell invasion of hu-man oesophageal squamous cell carcinoma cell lines in vitro andin vivo[J].Eur J Cancer,2006,42(10):1455-1465.
  • 8PRENDER GAST GC.Actin’up:RhoB in nancer and apoptosis[J].Nat Rev Cancer,2001,1(2):162-168.
  • 9ADNANE J,MURO-CACHO C,MATHEWS L,et al.Suppres-sion of rhoB expression in invasive carcinoma from head andneck cancer patients[J],Clin Cancer Res,2002,8(7):2225-2232.
  • 10CLARK EA,GOLUB TR,LANDER ES,et al.Genomic analysisof metastasis reveals all essential role for RhoC[J].Nature,2000,406(6795):532-535.

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  • 1MOJSA B, LASSOT I, DESAGHER S. Mcl-1 ubiquitination: u- nique regulation of an essential survival protein[J]. Cells, 2014, 3 (2): 418-437.
  • 2PFANNENSTIEL LW, GASTMAN BR. Mcl-I and tumor cell persistence[J]. Oncotarget, 2015, 6(1): 5-6.
  • 3BELMAR J, FESIK SW. Small molecule Mcl-1 inhibitors for the treatment of cancer[J]. Pharmacol Ther, 2015, 145: 76-84.
  • 4MODUGNO M, BANFI P, GASPARRI F. Mcl-I antagonism is a potential therapeutic strategy in a subset of solid cancers[J]. Exp Cell Res, 2015, 332(2): 267-277.
  • 5FIELDS AC, COTSONIS G, SEXTON D, et at. Mcl-1 expression in hepatocellular carcinoma: correlation with proliferation, prog- nostic parameters, and outcome[J]. Mod Pathol, 2004, 17(11): 1378-1385.
  • 6ERIC B, HAURA, LANXI S, et al. MCI-I is a survival factor in lung cancer[J]. Oral Sessions Prognostic Factor, 2003, 8: 574-575.

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