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不同乳腺疾病中ERK、PI3-K mRNA的表达 被引量:1

Expression of ERK and PI3-K mRNA in various breast dieases and its significance
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摘要 目的:检测正常乳腺组织、良性增生、非典型增生和乳腺癌中ERK、PI3-KmRNA的表达,探讨其在乳腺癌发生、发展中的作用及关系。方法:应用RT-PCR方法检测ERK、PI3-KmRNA在正常乳腺组织及不同乳腺疾病中的表达。结果:ERK2和PI3-KmRNA在乳腺癌组织中表达明显高于其他乳腺组织,分别为100%(37/37)和94.59%(35/37)。ERK2mRNA在乳腺癌、非典型增生、良性增生和正常组织的表达强度依次减弱;PI3-KmRNA表达在乳腺癌中明显增高,而在非典型增生和良性增生和正常组织中的表达无明显差别。结论:MAPK/ERK途径参与乳腺癌发生的信号转导,而PI3-K途径参与乳腺癌后期进展阶段的信号转导。 Objective: To investigate the expression and significance of ERK and PI3 - K mRNA in various breast lesions and breast carcinoma. Methods : RT - PCR was used to detect the expressions of ERK and PI3 - K mRNA in 37 cases of breast cancer,6 cases of atypical hyperplasia and 15 cases of benigh breast diseases. Results: The rates of positive expression of ERK and PI3 - K in breast cancer were 100% ( 37/37 ) and 94.59% ( 35/37 ) respectively and higher than other tissues. The tendency of decreased expression of ERK mRNA was breast cancer, atypical hyperplasia, benigh diseases and normal tissue. The difference of the levels of expression of PI3 - K mRNA in atypical hyperplasia and benigh diseases was not significant. Conclusion : ERK and PI3 - K pathways are involved in breast carcinogensis.
出处 《现代肿瘤医学》 CAS 2006年第12期1528-1530,共3页 Journal of Modern Oncology
基金 辽宁省教育厅高等学校科研项目基金(编号:2004D107)
关键词 乳腺疾病 信号转导 MAPK PI3-K ERK breast lesions signal transduction ERK PI3- K
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  • 1Sewell JM,Smyth JF,Langdon SP.Role of TGF alpha stimulation of the ERK,PI3 kinase and PLC gamma pathways in ovarian cancer growth and migration[J].Exp Cell Res,2005,304 (1):305~316.
  • 2Shin I,Kim S,Song H,et al.H-Ras-specific activation of Rac -MKK3/6-p38 pathway:its critical role in invasion and migration of breast epithelial cells[J].J Biol Chem,2005,280 (15):14675~14683.
  • 3Cowly S,Paterson H,Kemp P,et al.Activation MAP kinase is necessary and significant for PC12 differentiation and for transformation of NIH 3T3 cells[J].Cell,1994,77:841~852.
  • 4Benini S,Manara MC,Cerisano V,et al.Contribution of MEK/MAPK and PI3-K signaling pathway to the malignant behavier of Ewing's sarcoma cells:therapeutic prospects[J].Int J Cancer,2004,108(3):358~366.
  • 5Allen RT,Krueger KD,Dhume A,et al.Sustained Akt/PKB activation and transient attenuation of c-jun N-terminal kinase in the inhibition of apoptosis by IGF-1 in vascular smooth muscle cells[J].Apoptosis,2005,10(3):525~535.
  • 6Tan M,Grijalia R,Yu D.Heregulinlβ1 -activated phosphytidylinositol-3 kinase enhances aggregation of MCF-7 breast cells independent of extracellullar signal-regulated kinase[J].Cancer Res,1999,59:1620~1625.
  • 7Dufourny B,Alblas J,Hetty AAM,et al.Mitogenic signaling of insulin -like growth factor Ⅰ in MCF -7 human breast cancer cells requires phosphatidylinositol 3-kinase and is independent of mitogene-activated protein kinase[J].Int J Cancer,1997,272(49):31163~31171.
  • 8姚青,骆军容,陈江浩,张聚良,袁时芳,凌瑞,王岭.MAPK信号通路相关信号转导分子在人乳腺癌细胞系中的表达及活化水平[J].细胞与分子免疫学杂志,2004,20(3):328-330. 被引量:15

二级参考文献7

  • 1Seger R, Krebs EG. The MAPK signaling cascade[J]. FASEBJ, 1995, 9: 726-735.
  • 2Piwien-Pilipuk G, Huo JS, Schwartz J. Growth hormone signal transduction[J]. J Pediatr Endocrinol Metab, 2002, 15: 771-786.
  • 3Weinstein-Oppenheimer CR, Blalock WL, Steelman LS, et al. The Raf signal transduction cascade as a target for chemotherapeutic intervention in growth factor-responsive tumors[J]. Pharmacol Ther, 2000, 88: 229-279.
  • 4Cowly S, Paterson H, Kemp P, et al. Activation of MAP kinase kinase is necessary and sufficient for PC12 differentiation and for transformation of NIH 3T3 cells[J]. Cell, 1994, 77: 841-852.
  • 5Salh B, Marotta A, Matthewson C, et al. Investigation of Mek-MAP kinase-RSK pathway in human breast cancer[J]. Anticancer Res, 1999, 19: 731-740.
  • 6Fiddes RJ, Janes PW, Sivertsen SP, et al. Inhibition of the MAP kinase cascade blocks heregulin induced cell cycle progression in T47D human breast cancer cell[J]. Oncogene, 1998, 16: 2803-2813.
  • 7Das R, Vonderhaar BK. Activation of raf1, MEK, and MAP kinase in prolactin responsive mammary cells[J]. Breast Cancer Res, 1996, 40: 141-149.

共引文献14

同被引文献7

  • 1杨竹林,邓星辉,杨乐平,苗雄鹰,刘栋才.胰腺癌组织化学趋化因子表达与肿瘤相关巨噬细胞计数的相关性[J].世界华人消化杂志,2004,12(10):2349-2352. 被引量:4
  • 2McCubrey JA, Steetman LS, Chappett WH, et al. Roles of the Raf/ MEK/ERK pathway in cell growth, malignant transformation and drug resistance[J]. Biochim Biophys Acta, 2007,1773(8) :1263 - 1284.
  • 3ho Y, Sasaki Y, Horimoto M, et al. Activation of mitogen -activated protein kinases/extracettutar signal - regulated kinases in human hepatocetlular carcinoma[ J ]. Hepatotogy, 1998,27 (4) :951 - 958.
  • 4Schmitz KJ, Wohtschtaeger J, Lang H, et al. Activation of the ERK and AKT signalling pathway predicts poor prognosis in hepatocettutar carcinoma and ERK activation in cancer tissue is associated with hepatitis C virus infection[J]. J Hepatot,2008,48( 1 ) :83 -90.
  • 5Kauffmann - Zeh A, Rodriguez - Vieiana P, Ulrich E, et al. Suppression of c - Myc - induced apoptosis by Ras signalling through PI ( 3 ) K and PKB[ J]. Nature, 1997,385(6616) :544-548.
  • 6Mitsui H, Takuwa N, Maruyama T,et al. The MEK1 -ERK map kinase pathway and the PI 3 - kinase - Akt pathway independently mediate anti - apoptotic signals in HepG2 liver cancer cells[J]. Int J Cancer, 2001,92(1) :55 -62.
  • 7Liu L, Xie Y, Lou L. PI3K is required for insulin -stimulated but not EGF- stimulated ERK1/2 activation[ J ]. Eur J Cell Biol, 2006,85 (5) :367-374.

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