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MTA1、nm23、c-myc在肝癌组织中的表达及其相关性 被引量:1

Expressions of MTA1,nm23 and c-myc in hepatocellular carcinoma and their correlations
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摘要 目的检测肝癌组织及相应癌旁组织中MTA1、nm23、c-myc的表达,探讨三者之间的相关性及与肝癌侵袭、转移和肝癌生物学行为的关系。方法采用免疫组织化学法检测60例肝癌组织及其相应癌旁组织中MTA1、nm23、c-myc蛋白的表达,并结合相关临床病理特征进行分析。结果①肝癌组织中MTA1蛋白、c-myc蛋白的阳性表达率显著高于其相应癌旁组织(P<0.01),而肝癌组织中nm23蛋白的阳性表达率显著低于其相应癌旁组织(P<0.01)。②在肝癌组织中MTA1蛋白、c-myc蛋白的高表达及nm23蛋白的低表达,均与肿瘤分化程度,肝内、外转移及门静脉癌栓相关(P<0.05)。此外,MTA1蛋白的高表达及nm23蛋白的低表达还与HBsAg水平有关(P<0.05),c-myc蛋白的高表达还与有无肿瘤包膜有关(P<0.05)。③Spearman相关分析显示,MTA1与nm23的表达呈负相关(rs=-0.625,P<0.01),MTA1与c-myc的表达呈正相关(rs=0.392,P<0.05),而nm23与c-myc之间未见明显相关性。结论 MTAl、c-myc蛋白水平的高表达和nm23蛋白水平的低表达与肝癌的侵袭、转移有关,三者的联合检测可用于判断肝癌的生物学行为,有助于肝癌的基础研究及临床治疗。 Objective To investigate expressions of metastasis-associated 1(MTA1),nm23 and c-myc in hepatocellular carcinoma tissues and corresponding tumor-adjacent tissues,and to explore their correlations with invasion,metastasis and biological behavior of hepatocellular carcinoma.Methods Expressions of MTA1,nm23 and c-myc proteins were detected in 60 hepatocellular carcinoma tissues and corresponding tumor-adjacent tissues by immunohistochemistry.Relationships between their expressions and clinical pathological features were analyzed.Results ① Expressions of MTA1 and c-myc proteins in hepatocellular carcinoma tissues were significantly higher than those in corresponding tumor-adjacent tissues(P 〈0.01),while expression of the nm23 protein in hepatocellular carcinoma tissues was significantly lower than that in corresponding tumor-adjacent tissues(P 〈0.01).② High expressions of MTA1 and c-myc proteins and low expression of the nm23 protein were associated with tumor differentiation,intrahepatic metastasis,extrahepatic metastasis and portal vein tumor thrombus(P 〈0.05).In addition,high expression of the MTA1 protein and low expression of the nm23 protein were related to the level of HBsAg(P 〈0.05),and high expression of the c-myc protein was related to presence or absence of the tumor capsule(P 〈0.05).③ Spearman correlation analysis showed that there was a negative correlation between expressions of MTA1 and nm23(r s=-0.625,P 〈0.01),and a positivecorrelation between expressions of MTA1 and c-myc(r s =0.392,P 〈0.05),while there was no significant correlation between expressions of nm23 and c-myc.Conclusions High expressions of MTA1 and c-myc proteins and low expression of the nm23 protein were closely associated with invasion and metastasis of hepatocellular carcinoma.Combined detection of the three indexes can be used to estimate the biological behavior of hepatocellular carcinoma,and be helpful in basic research and clinical treatment of hepatocellular carcinoma.
出处 《山东大学学报(医学版)》 CAS 北大核心 2011年第1期99-103,110,共6页 Journal of Shandong University:Health Sciences
基金 山东省博士基金计划项目(2008BS03014)
关键词 肿瘤转移相关基因1 NM23 c—myc 肝细胞癌 侵袭 转移 免疫组织化学 Metastasis-associated 1 nm23 c-myc Hepatocellular carcinoma Invasion Metastasis Immunohisto-chemistry
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  • 1Toh Y, Pencil SD, Nicolson GL. A novel candidate metastasis-associated gene, mtal, differentially expressed in high metastatic mammary adenocarcinoma cell line. J Biol Chem 1994 ; 269:22958-22963.
  • 2Toh Y, Pencil SD, Nicolson GL. Analysis of the complete sequence of the novel metastasis associated candidate gene mtal differentitally expressed in mammary adenocarcinoma and breast cancer cell lines. Gene 1995; 159: 97-104.
  • 3Toh Y, Oki E, Ods S, et al. Overexpression of MTAL gene in gastrointestinal carcinoma: correlaion with invasion and metastasis. Int J Cancer 1999; 74:459-463.
  • 4Toh Y, Kiwano H, Mori M,et al.Overexpression of metastasis-associated MTA1 mRNA in invasive esophageal carcinomas. Br J Cancer 1999; 79:1723-6.
  • 5Lakshmi MS, Parker C, Sherbet GV. Mentastasis associated mtsl and nm23 gene affect tubulin polymerization Ⅱ in B16 melanomas: a possible mechanism of their regulation of metastasis behavior of tumors. Anticancer Res 1993; 13:299-303.
  • 6Hsu JW, Hsu SL, Chu JJ, et al. Increasd nm23: MTS1 ratio inversely correlated with metastasis behavior in human long sequamous cell carcinoma. Anticancer Res 1997; 17:407-411.
  • 7Sawan A. Lascu I , Veron M, et al. NDPK/nm23 expression in human breast cancer in relation to relapse, survival, and other prognostic factors: an immunohistochemical study. J Pathol 1994; 172:27-34.
  • 8Viel A, Agnese LD, Canzonieri V, et al. Suppression role of the metastasis related nm23H1 gene in human ovarian carcinoma: association of high messenger RNA expression with lack of lymph node metastasis. Cancer Res 1995; 55:2645-2650.
  • 9段小娴,欧盛敬,李瑗,曹骥,苏建家,欧超,杨春,岳惠芬.树实验肝癌形成过程中p53、bcl-2蛋白表达及其与细胞凋亡之间的关系[J].中国肿瘤临床,2004,31(18):41-43. 被引量:4
  • 10Qi-FuLi,Gao-LiangOuyang,Xuan-XianPeng,Shui-GenHong.Effects of tachyplesin on the regulation of cell cycle in human hepatocarcinoma SMMC-7721 cells[J].World Journal of Gastroenterology,2003,9(3):454-458. 被引量:15

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  • 1Osawa Y, Seki E, Kodama Y, et al. Acid sphingomyeli- nase regulates glucose and lipid metabolism in hepatocytes through AKT activation and AMP-activated protein kinase suppression[J]. FASEB J. 2011. 25(4) -.1133-1144.
  • 2Maceyka M, Milstien S, Spiegel S. Sphingosine-l-phos- phate : the Swiss army knife of sphingolipid signaling[J]. J Lipid Res, 2009, 50 : S272-276.
  • 3D' Amico T A. Outcomes after surgery for esophageal cancer[ J ]. Gastrointest Cancer Res, 2007, 1 (5) : 188-196.
  • 4Kim S H, Kim J H, Yu E J, et al. The overexpression of DBC1 in esophageal squamous cell carcinoma correlates with poor prognosis [ J ]. Histol Histopathol, 2012, 27 ( 1 ) :49-58.
  • 5Lee K W, Kim J H, Han S, et al. Twistl is an independ- ent prognostic factor of esophageal squamous cell carcino- ma and associated with its epithelial-mesenchymal transi- tion[J]. Ann Surg Oncol, 2012, 19(1) :326-335.
  • 6Estrada-Bernal A, Lawler S E, Nowicki M O, et al. The role of sphingosine kinase-I in EGFRvlII-regulated growth and survival of glioblastoma cells [ J ]. J Neurooncol, 2011, 102(3) :353-366.
  • 7Hu J, Jo M, Cavenee W K, et al. Crosstalk between the urokinase-type plasminogen activator receptor and EGF re- ceptor variant III supports survival and growth of glioblas- toma cells[J]. Proc Natl Acad Sci U S A, 2011, 108 ( 38 ) : 15984-15989.
  • 8Shida D, Takabe K, Kapitonov D, et al. Targeting SphK1 as a new strategy against cancer [ J ]. CUlT Drug Targets, 2008, 9(8):662-673.
  • 9Pan J, Tao Y F, Zhou Z, et al. An novel role of sphingo- sine kinase-1 (SPHK1) in the invasion and metastasis of esophageal carcinoma [ J ]. J Transl Med, 2011,22 (9) : 157.
  • 10Valastyan S, Weinberg R A. Tumor metastasis : molecu- lar insights and evolving paradigms[J]. Cell, 2011, 147 (2) :275-292.

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