期刊文献+

双特异性蛋白磷酸酶6在肿瘤中作用的研究进展

Progress in study on DUSP6 in the tumor
下载PDF
导出
摘要 双特异性蛋白磷酸酶6(dual specificity phosphatases 6,DUSP6)是一种双特异性蛋白磷酸酶,主要是负反馈调控反转录病毒相关的DNA序列-细胞外信号调节激酶1/2(retrovirus associated DNA sequences-extracellular signal regulated kinase,RAS-ERK1/2)信号通路。而DUSP6对于RASERK1/2信号转导通路的负反馈调节一旦打破,就可能会引起肿瘤,甚至还会出现恶性分化。近年来DUSP6在肿瘤形成、浸润、转移和肿瘤治疗方面的作用,已成为新的研究热点,能有助于许多恶性肿瘤的临床病理的诊断及治疗预后的判断。 Dual specificity protein phosphatase 6(DUSP6 ) is a dual specificity protein phosphatase, which exerts an important negative feedback effect on retrovirus associated DNA sequences-extracellular signal regulated kinase (RAS-ERK1/2) signaling pathway. Once the negative feedback regulation is broken, it may cause cancer, or even malignant differentiation. In recent years, DUSP6 has become a new hotspot in tumor formation, invasion, metastasis and treatment, which may have value in clinical diagnosis and prognosis for many malignant tumors.
出处 《临床与病理杂志》 CAS 2014年第2期206-211,共6页 Journal of Clinical and Pathological Research
关键词 双特异性蛋白磷酸酶6 促分裂原活化蛋白激酶 ERK 肿瘤 dual specificity protein phosphatase 6 mitogen-activated protein kinase ERK tumor
  • 相关文献

参考文献14

  • 1杨博,纪元,谭云山.DUSP6在肝细胞肝癌中的表达与MAPK信号通路及临床病理学特征相关性研究[J].中国肿瘤临床,2012,29(24):2085-2090. 被引量:2
  • 2张珍,王东.DUSP6/MKP-3在肿瘤研究中的进展及其在乳腺癌研究中的展望[J].四川医学,2010,31(9):1380-1382. 被引量:1
  • 3高振芹,胡永斌,周建华.MAPK信号通路与上皮间质转型[J].国际病理科学与临床杂志,2009,29(4):303-306. 被引量:6
  • 4曾亮,曹亚.MAPK信号通路与肿瘤侵袭和转移研究进展[J].肿瘤防治研究,2002,29(5):419-421. 被引量:12
  • 5Hui Zhang,Qiufen Guo,Chong Wang,Lei Yan,Yibing Fu,Mingjun Fan,Xingbo Zhao,Mingjiang Li.Dual-specificity phosphatase 6 (Dusp6), a negative regulator of FGF2/ERK1/2 signaling, enhances 17β-estrodial-induced cell growth in endometrial adenocarcinoma cell[J].Molecular and Cellular Endocrinology (-).2013(1-2)
  • 6Jianjuan Ma,Xiying Yu,Liping Guo,Shih Lu.DUSP6, a tumor suppressor, is involved in differentiation and apoptosisin esophageal squamous cell carcinoma[J].Oncology Letters.2013(6)
  • 7Jung Uee Lee,Songmei Huang,Min Hee Lee,Seong Eun Lee,Min Jeong Ryu,Soung Jung Kim,Yong Kyung Kim,Seul Young Kim,Kyong Hye Joung,Jin Man Kim,Minho Shong,Young Suk Jo.Dual specificity phosphatase 6 as a predictor of invasiveness in papillary thyroid cancer[J].European Journal of Endocrinology.2012(1)
  • 8Eva Zeller,Katharina Mock,Moritz Horn,Sabine Colnot,Michael Schwarz,Albert Braeuning.Dual-specificity phosphatases are targets of the Wnt/β-catenin pathway and candidate mediators of β-catenin/Ras signaling interactions[J].Biological Chemistry.2012(10)
  • 9LiangSong,Ann‐MarieRitchie,David W.Melton.Increased levels of DUSP6 phosphatase stimulate tumourigenesis in a molecularly distinct melanoma subtype[J].Pigment Cell & Melanoma Research.2012(2)
  • 10Hyunjung Lee,Jin Man Kim,Song-Mei Huang,Seung-Kiel Park,Dong-Hoon Kim,Do Hyung Kim,Choong Sik Lee,Kwang Sun Suh,Eunhee S. Yi,Kyung-Hee Kim.Differential expression of DUSP6 with expression of ERK and Ki-67 in non-small cell lung carcinoma[J].Pathology - Research and Practice.2011(7)

二级参考文献52

  • 1[1]Jukka W, Veli-Matti K. Regulation of matrix metalloproteinase expression in tumor invasion. FASEB J, 1999, 13:781-792.
  • 2[2]Johansson N, Ala-aho R, Uitto V, et al. Expression of collagenase-3(MMP-13) and collagenase-1(MMP-1) by transformed keratinocytes is dependent on the activity of p38 mitogen-activated protein kinase. J Cell Sci , 2000, 113 pt 2:227-235.
  • 3[3]Simon C, Hicks MJ, Nemechek AJ, et al. PD098059, an inhibitor of ERK1 activation, attenuates the in vivo invasiveness of head and neck squamous cell carcinoma. Br J Cancer, 1999, 80(9):1412-1419.
  • 4[4]Vo HP, Lee MK, Crowe DL.alpha2beta1 integrin signaling via the mitogen activated protein kinase pathway modulate retinoic acid-dependent tumor cell invasion and transcriptional downregulation of matrix metalloproteinase 9 activity . Int J Oncol, 1998, 13(6):1127-1134.
  • 5[5]Tsang KJ, Crowe DL. Retinoic acid and extracellular matrix metalloproteinase 9 expression is mediated by the mitogen activated protein kinase pathway. Int J Oncol, 2001, 18(2):369-374.
  • 6[6]Bancroft CC, Chen Z, Dong G, et al. Coexpression of proangiogenic factors IL-8 and VEGF by human head and neck squamous cell carcinoma involves coactivation by MEK-MAPK and IKK-NF-kappaB signal pathways. Clin Cancer Res, 2001,7(2):435-442.
  • 7[7]Yoshiji H, Kuriyama S, Ways DK, et al. Protein kinase C on the signaling pathway for vascular endothelial growth factor-mediated tumor development and angiogenesis. Cancer Res, 1999, 59(17):4413-4418.
  • 8[8]Okajima E, Thorgeirsson UP. Different regulation of vascular endothelial growth factor expression by the ERK and p38 kinase pathways in V-ras, v-raf, and v-myc transformed cells. Biochem Biophys Res Commun, 2000, 270(1):108-111.
  • 9[9]Harris VK, Coticchia CM, Kagan BL, et al. Induction of the angiogenic modulator fibroblast growth factor-binding protein by epidermal growth factor is mediated through both MEK/ERK and p38 signal transduction pathways. J Biol Chem, 2000, 275(15):10802-10811.
  • 10[10]Zhou JN, Ljungdahl S, Shoushan MC, et al. Activating of tissue-factor gene expression in breast carcinoma cells by stimulation of the RAF-ERK signaling pathway. Mol Carcinog, 1998, 21(4):234-243.

共引文献17

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