期刊文献+

RECK和基质金属蛋白酶与恶性肿瘤预后的研究进展 被引量:7

Correlation of RECK and matrix matalloproteinases with the prognosis of malignant tumor
下载PDF
导出
摘要 伴有kazal基序富含半胱氨酸的逆转诱导蛋白(reversion-inducing cysteine-rich protein with Kazal motif,RECK)基因是新近发现的基质金属蛋白酶(matrix matalloproteinase,MMP)抑制剂,能在转录后水平抑制多种MMP的表达而抑制肿瘤的侵袭及转移。RECK与乳腺癌、胰腺癌、骨肉瘤等疾病患者的预后存在正相关关系。文中综述RECK和MMP与各系统肿瘤的关系。 The reversion-inducing-cysteine-rich protein with Kazal motifs (RECK) gene, a newly found matrix matalloprotein- ase (MMP) inhibitor, can inhibit tumor invasion and metastasis by negatively regulating the expressions of various MMPs. RECK is positively correlated with the prognosis of breast cancer, pancreatic cancer and osteosarcoma.
出处 《医学研究生学报》 CAS 北大核心 2013年第3期330-333,共4页 Journal of Medical Postgraduates
关键词 回复引导半胱氨酸丰富蛋白含kazal基序 基质金属蛋白酶 恶性肿瘤 预后 Reversion-inducing cysteine-rich protein with Kazal motif Matrix matalloproteinase Malignant tumor Prognosis
  • 相关文献

参考文献18

  • 1Furumoto K, Arii S, Mori A, et al. RECK gene expression in hepatocellular carcinoma: correlation with invasion-related clini- copathological factors and its clinical significance. Reverse-indu- cing--cysteine-rich protein with Kazal motifs [ J ]. Hepatology, 2001, 33 ( 1 ) : 189-195.
  • 2Takahashi C, Sheng Z, Horan TP, et al. Regulation of matrix metalloproteinase-9 and inhibition of tumor invasion by the mem- brane-anchored glycoprotein RECK [ J ]. Proc Natl Acad Sci USA, 1998, 95(22) :13221-13226.
  • 3Sasahara RM, Takahashi C, Oh J, et al. Transcriptional control of the RECK metastasis/angiogenesis suppressor gene [ J ]. Cancer Detect Prey,2002, 26(6) :435-443.
  • 4Oshima T, Kunisaki C, Yoshihara K, et al. Clinicopathologieal significance of the gene expression of matrix metalloproteinases and reversion-inducing cysteine-rich protein with Kazal motifs in patients with colorectal cancer: MMP-2 gene expression is a use- ful predictor of liver metastasis from colorectal cancer[ J]. Oncol Rep, 2008, 19(5) :1285-1291.
  • 5Oh J, Takahashi R, Kondo S, et al. The membrane-anchored MMP inhibitor RECK is a key regulator of extracellular matrix in- tegrity and angiogenesis[ J]. Cell,2001, 107(6) :789-800.
  • 6霍志军,陈道瑾,李小荣,唐利立,吴唯.乳腺癌和纤维瘤中RECK-mRNA和MMP9-mRNA的表达差异及意义[J].中国普通外科杂志,2007,16(1):69-72. 被引量:5
  • 7Chang CK, Hung WC, Chang HC. The Kazal motifs of RECK protein inhibit MMP-9 secretion and activity and reduce metasta- sis of lung cancer cells in vitro and in vivo[J]. J Cell Mol Med, 2008, 12(6B):2781-2789.
  • 8Egeblad M, Werb Z. New functions for the matrix metalloprotein- eases in cancer progression [ J ]. Nat Rev Cancer, 2002, 2 ( 3 ) : 161-174.
  • 9Takagi S, Simizu S, Osada H. RECK negatively regulates matrix metalloproteinase-9 transcription [ J ]. Cancer Res, 2009, 69 (4) :1502-1508.
  • 10孙涛,姜大庆,李金鸣,韩冬云,宋志国,陶秀娟.人乳腺癌细胞RECK基因的表达及检测[J].中国肿瘤临床,2006,33(22):1288-1290. 被引量:5

二级参考文献75

  • 1徐振宇,高建平,孙颖浩.RECK基因的研究进展[J].医学研究生学报,2005,18(4):361-363. 被引量:6
  • 2徐振宇,高建平,张征宇,葛京平,许传亮,孙颖浩.RECK基因在前列腺癌组织中的表达及其与基质金属蛋白酶的关系[J].医学研究生学报,2005,18(7):577-579. 被引量:6
  • 3徐振宇,许传亮,孙颖浩.RECK基因在前列腺组织中的表达及其与基质金属蛋白酶-9的关系[J].中华实验外科杂志,2005,22(9):1146-1146. 被引量:5
  • 4徐振宇,高建平,张征宇,葛京平,许传亮,孙颖浩.基质金属蛋白酶抑制剂RECK基因在前列腺细胞株中的表达及意义[J].中华男科学杂志,2005,11(10):727-730. 被引量:9
  • 5Loukopoulos P, Mungall BA, Straw RC, et al. Matrix metallopro-teinane-2 and-9 involvement in canine tumors [ J ]. Vet Pathol, 2003,40(4) :382 -394.
  • 6Ivaska J, Heino J. Adhesion receptors and cell invasion: Mechanisms of integrin - guided degradation of extracellular matrix [ J ]. Cell Mol Life Sci, 2000, 57(1) : 16 -24.
  • 7Fang J, Shing Y, Wiederschain D, et al. Matrix metalloproteinase-2 is required for the switch to the angiogenic phenotype in a tumor model[J]. Proc Natl Acad Sci USA, 2000,97(8) :3884 -3889.
  • 8Oh J, Takahashi R, Kondo S, et al. The membrane-anchored MMP inhibitor RECK is a key regulator of extracellular matrix integrity and angiogenesis[ J]. Cell, 2001,107(6) :789 -800.
  • 9Correa TC, Brohem CA, Winnischofer SM, et al. Downerregulation of the RECK-tumor and metastasis suppressor gene in glima invasiveness[ J]. J Cell Biochem, 2006,99( 1 ) : 156 - 167.
  • 10Kanda K, Takahashi M, Murakami Y, et al. The role of the activated form of matrix metalloproteinases-2 in urothelial cancer[ J]. BJU Int, 2000, 86(4) : 553 -557.

共引文献31

同被引文献93

  • 1王金万,孙燕,刘永煜,于起涛,张沂平,李凯,朱允中,周清华,侯梅,管忠震,李维廉,庄武,王东林,梁后杰,秦凤展,卢辉山,刘晓晴,孙红,张燕军,王杰军,罗素霞,杨瑞合,涂远荣,王秀问,宋恕平,周静敏,游丽芬,王竞,姚晨.重组人血管内皮抑素联合NP方案治疗晚期NSCLC随机、双盲、对照、多中心Ⅲ期临床研究[J].中国肺癌杂志,2005,8(4):283-290. 被引量:625
  • 2李晟磊,赵秋民,刘宗文,赵志华,高冬玲,郑湘予,陈奎生,张云汉.食管鳞癌中RECK和MMP-9蛋白表达的相关性及临床病理意义[J].世界华人消化杂志,2007,15(10):1082-1086. 被引量:34
  • 3Watanabe R, Tokuhira M, Kizaki M. Current approaches for tile treatment of multiple myeloma [ J ]. lnt J Henmtol, 2013, 97 ( 3 ) : 333-344.
  • 4Aggeli IK, Koustas E, Gaitanaki C, el al. Curcumin acts as a pro-oxidant inducing apoptosis via JNKs in the isolated peffused Rana ridibunda heart [ J ]. J Exp Zool A Ecol Genel Physiol, 2013. 319(6) : 328-339.
  • 5Chen F. JNK-lnduced Alxptosis, comtnsatory growth, and cancer stem cells[J]. Cancer Res, 2012, 72(2) : 379-386.
  • 6Dhanasekaran I)N, Reddy EP. JNK signaling in apoptosis[J]. Oncogene, 2008, 27 (48) : 6245-6251.
  • 7Park MT, Song M J, Lee It, et al. -Iapachone signifieantly in- creases the effecl of ionizing radiation to cause milochondfial ap- optosis via JNK activation in cancer cells[ J ]. PIxS One, 2011, 6(10) : e25976-25979.
  • 8Lu J J, Cai YJ. Ding J. The shorl-time treatment with curcumin sufficiently decreases cell viability, induces apoptosis and copper enhanees these effects in muhidrug-resistant K562/A02 cells [J]. M.I Cell Biochem, 2012, 360( 1-2): 253-360.
  • 9Gao SM, Yang J J, Chen CQ, et al. Pure curcumin decreases the expression of WTI by upregulation of miR-15a and miR-16-1 in leukemic cells[J]. J Exp Clin Cancer Res, 2012, 31 : 27.
  • 10Trojanek J. Ma|rix metal|oproteinases and their tissue inhibitors [J]. Postepy Biochem, 2012, 58(3): 353-362.

引证文献7

二级引证文献33

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部