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基质金属蛋白酶7在肿瘤中的作用及其机制研究进展 被引量:6

Research Advances in Effects and Mechanisms of MMP7 in Tumor Progression
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摘要 基质金属蛋白酶(Matrix Metalloproteinases,MMPs)是与肿瘤相关的一个蛋白酶家族,这个家族拥有29个成员,它们广泛参与肿瘤细胞的生长、侵袭和转移以及血管生成过程。基质金属蛋白酶7(MMP7)由于其结构特点和生理活性,被认为是这个家族中最重要的成员之一。在MMPs广谱抑制剂临床实验均不理想的情况下,对MMP7与肿瘤关系的深入研究,有助于更好的针对MMP7的肿瘤药物的研发。文章介绍了MMP7在肿瘤生长、侵袭转移和肿瘤血管生成中相关作用机制,并对MMP7在肿瘤诊断和治疗中的最新研究进展做了简要综述。 The matrix metalloproteinase (MMP) family of 29 proteases has long been associated with cancer invasion, metastasis and tumor angiogenesis by virtue of their ability to collectively degrade all components of the extracellular matrix ( ECM ). Matrix metalloproteinase 7 (MMPT) is one of the most important proteases because of its structure and function. A vast number of MMPIs ( MMP inhibitors) have been developed in recent years. Due to the failure of these inhibitors in clinical trials, more efforts have been directed to the relationship between MMP7 and tumor, which can promote the design of MMPI. This review summarizes the role of MMP7 in tumor progression, and the application of MMP7 in tumor diagnosis and treatment.
出处 《药物生物技术》 CAS CSCD 2011年第5期457-460,共4页 Pharmaceutical Biotechnology
关键词 基质金属蛋白酶7 肿瘤 肿瘤转移 Matrix metalloproteinase 7,Tumor,Tumor metastasis
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  • 1Gross J, Lapiere C M. Collagenolytic activity in amphibian tissues: a tissue culture assay [ J ]. Proc Natl Acad Sci, 1962,45 ( 1 ) :1014.
  • 2Thrailkill KM, Bunn RC, Fowlkes JL. Matrix metalloproteinases: their potential role in the pathogenesis of diabetic nephropathy [J]. Endocrine,2009,35( 1 ) : 1.
  • 3Kessenbrock K, Plaks V, Werb Z. Matrix metalloproteinases : regulators of the tumor microenvironment [ J]. Cell ,2010,141 (1) :52.
  • 4Rajeshwar PV, Hansch C. Matrix metalloproteinases (MMPs) : Chemical-biological functions and ( Q ) SARs [ J ]. Bioorganic & Medicinal Chemistry,2007,15 ( 7 ) :2223.
  • 5Sternlicht M, Werb Z. How matrix metalloproteinases regulate cell behavior [ J ]. Annu Rev,2001 , 17 ( 1 ) : 463.
  • 6Ii M, Yamamoto H, Adachi Y, Mamyama Y,et al. Role of matrix metalloproteinase-7 in human cancer invasion, apoptosis, growth, and angiogenesis [ J]. Exp Biol Med ,2006 ,231 ( 1 ) :20.
  • 7Leelawat K, Sakchinabut S, Narong S, et al. Detection of serum MMP-7 and MMP-9 in cholangiocarcinoma patients : evaluation of diagnostic accuracy[ J]. Gastroenterology,2009,9(5 ) : 30.
  • 8Maurel J, Nadal C, Garcia-Albeniz X, et al. Serum matrix metalloproteinase 7 levels identifies poor prognosis advanced colorectal cancer patients[ Jl. Int J Cancer,2007,121(5 ) : 1066.
  • 9Liu D, Nakano J, Ishikawa S, et al. Overexpression of matrix metalloproteinase-7 ( MMP-7 ) correlates with tumor proliferation, and a poor prognosis in non-smal.l cell lung cancer[ J ]. Luag Cancer, 2007,58(3) : 384.
  • 10Gallego R, Codony-Servat J, Garcia-Albeniz X, et al. Serum IGF- 1, IGFBP-3, and matrix metalloproteinase-7 levels and acquired chemo-resistance in advanced colorectal cancer[ Jl. Endocr Relat Cancer,2009,16( 1 ) :311.

同被引文献59

  • 1宫大鑫,王侠,李泽良,刘屹立,金铎,孙志熙,王平,孔垂泽.嗜铬细胞瘤诊疗对策[J].中国肿瘤临床,2005,32(19):1112-1115. 被引量:12
  • 2符丽华,熊小英.MTA1基因在宫颈癌组织中的表达及其临床意义[J].中国妇幼健康研究,2006,17(5):349-351. 被引量:11
  • 3董颖,赵长宏.基质金属蛋白酶与肿瘤侵袭转移的研究进展[J].实用肿瘤学杂志,2007,21(4):384-386. 被引量:12
  • 4O'Connell RM, Chaudhuri AA, Rao DS, et al. MicroRNAs enriched in hematopoietic stem cells differentially regulate long-term hematopoietic output[J]. Proc Natl Acad Sci U S A,2010,107 : 14235. ].
  • 5Li XM, Wang AM, Zhang J, et al. Down-regulation of miR-126 expression in colorectal cancer and its clinical significance [ J ]. Med Oncol ,2011,28 : 1054.
  • 6Liang D,Meyer L,Chang DW,et al. Genetic variants in MicroRNA biosynthesis pathways and binding sites modify ovarian cancer risk, survival, and treatment response [J]. Cancer Res, 2010, 70:9765.
  • 7Liu C, Kelnar K, Liu B, et al. The microRNA miR-34a inhibits prostate cancer stem cells and metastasis by directly repressing CD44[J]. Nat Med,2011,17 :211.
  • 8Yamakuchi M,Yagi S, Ito T,et al. MicroRNA-22 regulates hypoxia signaling in colon cancer cells[ J]. PLoS ONE,2011,6:20291.
  • 9Liu L, Jiang Y, Zhang H, et al. miR-22 functions as a micro-oncogene in transformed human bronchial epithelial cells induced by anti-benzo[a] pyrene-7, 8-diol-9, 10-epoxide [J]. Toxicol In Vitro ,2010,24 : 1168.
  • 10Xiong J, Du Q, Liang Z. Tumor-suppressive microRNA-22 inhibits the transcription of E-box-containing c-Myc target genes by silencing c-Myc binding protein[J]. Oncogene,2010 ,29 :4980.

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