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OPN及β-catenin在涎腺黏液表皮样癌中的表达及意义 被引量:2

Expression of β-catenin and Osteopontin in Mucoepidermoid Carcinoma.
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摘要 目的:研究OPN及β-catenin在黏液表皮样癌中的表达,探讨其在黏液表皮样癌病变中的作用及其临床意义。方法:应用免疫组织化学S-P法检测35例黏液表皮样癌及12例正常涎腺组织中β-catenin及OPN的表达。结果:黏液表皮样癌中β-catenin和OPN的阳性表达率分别为37.1%(13/35)和65.7%(23/35)与正常对照组存在显著性差异(P<0.05)。在黏液表皮样癌中它们的表达呈显著相关性(P=0.0001,R=-0.691)。β-catenin和OPN的阳性率在不同分化程度的黏液表皮样癌中存有差异(P<0.05),且与是否存在淋巴结转移有显著性关系(P<0.05)。结论:β-catenin及OPN的表达与黏液表皮样癌的发生和发展关系密切,检测该指标有助于判断黏液表皮样癌的病理分级和淋巴结转移的关系。 Objective: To detect the expression of β- catenin and osteopontin (OPN) in mucoepidermoid carcinoma (MEC) and explore its clinicopathological significance. Methods : SP immunohistochemical staining of β - eatenin and OPN was carried out in 35 cases of MEC and 12 cases of normal salivary tissues. Results: The positive rates of β - catenin and OPN were 37.1% (13/35) and 65.7% (23/35). Correlationship was shared by positive β -eatenin and OPN in MEC (P =0.0001 ,R = -0. 691 ). There were significant differences for β - catenin and OPN positive rates in different grades of MEC and the positive rates were related with lymph node metastasis ( P 〈 O. 05 ). Conclusion: There was significant correlation between the expression of β - catenin and OPN and the WHO pathologic grade of mucoepidermoid carcinoma, which may indicate the clinic prognostic significance.
出处 《口腔医学研究》 CAS CSCD 2008年第6期640-643,共4页 Journal of Oral Science Research
关键词 黏液表皮样癌 Β-CATENIN OPN免疫组织化学 Mucoepidermoid carcinoma β - catenin OPN Immunohistochemistry
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  • 1张卫民,高岩.Wnt信号传导通路组成蛋白与口腔鳞状细胞癌的分化和增殖[J].中华口腔医学杂志,2005,40(6):491-494. 被引量:15
  • 2Weber GF, Zawaideh S, Hikita S, et al. Phosphorylation-dependent interaction of osteopontin with its receptor regulates macrophage migration and activation [J], J Leucoc Biol, 2002 ;72:752-61.
  • 3Hiramaa M, Takahashi F, Takahashia K, et al , Osteopontin overproduced by tumor cells acts as a potent angiogenenic factor contributing to tumor growth [J], Cancer Latt, 2003;198:107-17.
  • 4Lameire N, Vanholder R. Pathophysiologie features and prevention of human and experimental acute tubular necrosis [J], J Am Soc Nephrol,2001 ; 12:20-32.
  • 5Petrow PK, Hummel KM, Sehedel J, et al . Expression of osteopontin messenger RNA and protein in rheumatoid arthritis: effects of osteopontin on the release of collagenase-1 from articular chondrocytes and synovial fibroblasts [J]. Arthritis Rheum, 2000 ;43 ~ 1597-605.
  • 6Attur MG, Dave MN, Stuehin S, et al. Osteopontin: an intrinsic inhibitor of inflammation in cartilage [J]. Arthritis Rheum, 2001 ;44:578-84.
  • 7Takagi H, Suzuma K, Otani A, et al. Role of vitronectin receptor-type integrins and osteopontin in ischemia-induced retinal neovascularization[J], Jap J Ophthalmol, 2002;46:270-8.
  • 8Philip S, Bulbule A, Kundu GC, Osteopontin stimulates tumor growth and aetivation of promatrix metalloproteinase-2 through ndelear factor κB-mediated induction of membrane type-1 matrix metalloproteinase in murine melanoma cells [J]. J Biol Chem, 2001 ;276 :44926-35.
  • 9Hilip S, Kundu GC, Osteopontin induces nuclear factor κB-mediatedpromatrix metalloproteinase-2 aetiviation through IkBa/Ikk signalingpathways, and cureumin (diferululmethane) down-regulates these pathway [J]. J Biol Chem, 2003;278:14487-97.
  • 10Dalonzo RC, Kowalski AJ, Denhardt DT, et al. Regulation of collagenase-3 and osteocalcin gene expression by collagen and osteopontin in differentiating MC3T3-E1 cells [J]. J Biol Chem, 2002;277: 24788-98.

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  • 1Behrens J, Lustig B. The Wnt connection to tumorigenesis [ J] . Int J Dev Biol, 2004, 48 (5 - 6) : 477 - 487.
  • 2Lilia Topol, Xueyuan Jiang, Choi H, et al. Wnt -5a inhibits the canonical Wnt pathway by promoting GSK - 3 - independent β - catenin degradation [ J]. The Journal of Cell Biology, 2003, 162 (5) : 899 - 908.
  • 3Ishitani T, Kishida S, Hyodo - Miura J, et al. The TAK1 - NLK mitogen -activated protein kinase cascade functions in the Wnt - 5a/Ca^2+ pathway to antagonize Wnt/beta -catenin signaling [ J]. Mol Cell Biol, 2003, 23 ( 1 ) : 131 - 139.
  • 4Peifer M, Polakis P. Writ signaling in oncogenesis and embryogenesis- a look outside the nucleus [ J]. Science, 2000, 287:1606 - 1609.
  • 5Bankfalvi A, Krassort M, Vegh A, et al. Deranged expression of the E -cadherin/beta- catenin complex and the epidermal growth factor receptor in the clinical evolution and progression of oral squamous cell carcinomas [J]. Oral Pathol Med, 2002, 31 (8): 450 - 457.
  • 6Goodwin AM, D'Amore PA. Wnt signaling in the vasculature [ J ] .Angiogenesis, 2002, 5 ( 1 - 2 ) : 1 - 9.
  • 7Opperman LA. Cranial sutures as intramembranous bone growth sites[J]. Dev Dyn, 2000,219(4):472 -485.
  • 8Klein- Nulend J, Roelofsen J, Semeins CM, et al. Mechanical stimulation of osteopontin mRNA expression and synthesis in bone cell cultures[ J]. J Cell Physiol, 1997, 170(2) : 174 - 181.
  • 9Terai K, Takano - Yamamoto T, Ohba Y, et al. Role of osteopontin in bone remodeling caused by mechanical stress [ J ]. J Bone Miner Res , 1999, 14(6):839-849.
  • 10Sate M, Yasui N, Nakase T, et al. Expression of bone matrix proteins mRNA during distraction osteogenesis [ J ]. J Bone Miner Res , 1998, 13(8):1221-1231.

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