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骨桥蛋白mRNA在口腔鳞癌与正常黏膜中的表达及临床意义 被引量:4

Expression of osteopontin mRNA in oral squamous cell carcinoma and normal oral mucosa
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摘要 目的探讨骨桥蛋白(OPN)mRNA在口腔鳞状细胞癌(OSCC)及配对正常口腔黏膜组织中的表达及临床意义。方法用SYBR Green I荧光定量RT-PCR方法检测30例OSCC患者肿瘤组织及其配对的正常口腔粘膜中OPN mRNA的表达。结果Real time RT-PCR检测结果表明,OPN mRNA在OSCC和配对正常粘膜的表达水平分别为4.17±0.51和0.97±0.12,上调4.3倍(P<0.001)。在30例OSCC标本中,OPN mRNA在高分化鳞癌中的表达为2.16±0.17,中/低分化鳞状细胞癌中的表达为6.80±0.72,下调3.1倍,P<0.05;在颈淋巴结阳性组表达为6.38±0.56,颈淋巴结阴性组为2.89±0.32,上调2.2倍,P<0.05;在临床早期表达为2.34±0.17,临床晚期表达为4.73±0.35,下调2.0倍,P<0.05。结论在OSCC的癌变过程中OPN基因的表达水平显著上调,可能是OSCC诊断、治疗及预后判断的一个靶点基因;OPN在OSCC分类诊断中有应用价值。 Objective To investigate osteopontin (OPN) mRNA expression in oral squamous cell carcinoma (OSCC) and normal oral mucosa tissues. Methods Differential OPN gene expression were detected in 30 cancerous tissues and their paired normal tissues using real-time reverse transcription-PCR (real-time RT-PCR), and the data were analyzed statistically. Results Real-time RT-PCR results demonstrated that the relative expression level of OPN mRNA in the cancerous tissues were significantly higher than that in paired normal samples (4.17±0.51 vs 0.97±0.12, P〈0.001), showing a 4.3 -fold up-regulation. In the 30 OSCC specimens, OPN mRNA expression in the OSCC of histological grades I showed a 3.1-fold down-regulation, significantly lower than the expression in grade Ⅱ/Ⅲ tumors (2.16±0.17 vs 6.80±0.72, P〈0.05); its expression was significantly lower in early stage than in advanced stage OSCCs (2.34±0.17 vs 4.73±0.35, P〈0.05). In cases of cervical lymph node metastasis, the expression was significantly higher than that in cases without lymphatic metastasis (6.38±0.56 vs 2.89±0.32, P〈0.05). Conclusion OPN mRNA overexpression may play an important role in OSCC carcinogenesis and can be a potential target for OSCC therapy.
出处 《南方医科大学学报》 CAS CSCD 北大核心 2008年第7期1165-1167,共3页 Journal of Southern Medical University
基金 国家自然科学基金重点项目(30330580) 上海市科学技术委员会项目(036505013,034107002)~~
关键词 口腔鳞状细胞癌 骨桥蛋白 RT—PCR 实时荧光定量 oral squamous cell carcinoma osteopontin real-time reverse transcriptase-polymerase chain reaction
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参考文献13

  • 1Kazanecki CC, Uzwiak D J, Denhardt DT. Control of osteopontin signaling and fimction by post-translational phosphorylation and protein folding[J]. J Cell Biochem, 2007, 102(4): 912-24.
  • 2Xie H, Song J, Du R, et al. Prognostic significance of osteopontin in hepatitis B virus-related hepatocellular carcinoma [J]. Dig Liver Dis, 2007, 39(2): 167-72.
  • 3Wu CY, Wu MS, Chiang EP, et al. Elevated plasma osteopontin associated with gastric cancer development, invasion and survival [J]. Gut, 2007, 56(6): 782-9.
  • 4Petrik D, Lavori PW, Cao H, et al. Plasma osteopontin is an independent prognostic marker for head and neck cancers [J]. J Clin Oncol, 2006, 24(33): 5291-7.
  • 5Kita Y, Natsugoe S, Okumura H, et al. Expression of osteopontin in oesophageal squamous cell carcinoma [J]. Br J Cancer, 2006, 95 (5): 634-8.
  • 6Celetti A, Testa D, Staibano S, et al. Overexpression of the cytokine osteopontin identifies aggressive laryngeal squamous cell carcinomas and enhances carcinoma cell proliferation and invasiveness[J]. Clin Cancer Res, 2005, 11 (22): 8019-27.
  • 7Barak V, Frenkel S, Kalickman I, et al. Serum markers to detect metastatic uveal melanoma [J]. Anticancer Res, 2007, 27 (4A): 1897-900.
  • 8Tuck AB, Chambers AF, Allan AL. Osteopontin overexpression in breast cancer: Knowledge gained and possible implications for clinical management[J]. J Cell Biochem, 2607, 102(4): 859-68.
  • 9Matsuzaki H, Shima K, Muramatsu T, et al. Osteopontin as biomarker in early invasion by squamous cell carcinoma in tongue [J]. J Oral Pathol Med, 2007, 36(1): 30-4.
  • 10Ogbureke KU, Nikitakis NG, Warburton G, et al. Up-regulation of SIBLING proteins and correlation with cognate MMP expression in oral cancer [J]. Oral Oncol, 2007, 43(9): 920-32.

同被引文献23

  • 1Sakineh Kazemi-Noureini,Sergio Colonna-Romano,Abed-Ali Ziaee,Mohammad-Ali Malboobi,Mansour Yazdanbod,Parviz Setayeshgar,Bruno Maresca.Differential gene expression between squamous cell carcinoma of esophageus and its normal epithelium; altered pattern of mal,akrlc2, and rablla expression[J].World Journal of Gastroenterology,2004,10(12):1716-1721. 被引量:4
  • 2吕晓智,陈万涛,张陈平.口腔鳞癌与正常黏膜中细胞角蛋白基因13的表达[J].上海口腔医学,2005,14(4):378-381. 被引量:6
  • 3Dittmer A, Sehunke D, Dittmer J. PTHrP promotes homotypic aggregation of breast cancer cells in three-dimensional cultures. Cancer Lett, 2008,260(1/2) :56-61.
  • 4Shen X, Rychahou PG, Evers BM, et al. PTHrP increases xenograft growth and promotes integrin alpha6beta4 expression and Akt activation in colon cancer. Cancer Lett, 2007,258(2) :241-252.
  • 5Lu Y, Xiao G, Galson DL, et al. PTHrP-induced MCP-1 production by human bone marrow endothelial cells and osteoblasts promotes osteoclast differentiation and prostate cancer cell proliferation and invasion in vitro. Int J Cancer, 2007,121 (4) :724-733.
  • 6Kuriakose MA, Chen WT, He ZM. Selection and validation of differentially expressed genes in head and neck cancer. Cell Mol Life Sei, 2004,61 ( 11 ) : 1372-1383.
  • 7Barnes L, Eveson JW, Reichart P, et al. Pathology and genetics of head and neck tumors. Lyon: IARC Press, 2005:168-175.
  • 8Burtis WJ, Wu T, Bunch C, et al. Identification of a novel 17,000-dalton parathyroid hormone-like adenylate eyclase-stimulating protein from a tumor associated with humoral hyperealeemia of malignancy. J Biol Chem, 1987,262(15) :7151-7156.
  • 9Cataisson C, Gordon J, Roussiere M, et al. Ets-1 activates parathyroid hormone-related protein gene expression in tumorigenic breast epithelial cells. Mol Cell Endocrinol, 2003,204(1/2) :155-168.
  • 10Yamada T, Tsuda M, Ohba Y, et al. PTHrP promotes malignancy of human oral cancer cell downstream of the EGFR signaling. Biothem Biophys Res Commun, 2008,368(3) :575-581.

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