期刊文献+

BRAF基因突变与结直肠癌的研究进展 被引量:2

下载PDF
导出
摘要 结直肠癌是常见的消化道恶性肿瘤之一,在美国每年约有近13万的新发病例,大约56000人死于结直肠癌,是第2位导致癌症死亡的因素。结直肠癌在我国男、女性恶性肿瘤发病率排名中分列第三和第二位。
作者 吴伟 孙文勇
出处 《实用医学杂志》 CAS 北大核心 2011年第5期903-905,共3页 The Journal of Practical Medicine
  • 相关文献

参考文献23

  • 1Fang J Y,Richardson B C.The MAPK signalling pathways and colorectal cancer[J].Lancet Oncol,2005,(6):322-327.
  • 2Davies H,Bignell G R,Cox C,et al.Mutations of the BRAF gene in human cancer[J].Nature,2002,417(6892):949-954.
  • 3Garnett M J,Marais R.Guilty as charged:B-RAF is a human oncogene[J].Cancer Cell,2004,(4):313-319.
  • 4Wan P T,Garnett M J,Roe S M,et al.Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF[J].Cell,2004,116(6):855-867.
  • 5Ikehara N,Semba S,Sakashita M,et al.BRAF mutation associated with dysregulation of apoptosis in human colorectal neoplasms[J].Int J Cancer,2005,115(6):943-950.
  • 6Oikonomou E,Makrodouli E,Evagelidou M,et al.BRAF(V600E) efficient transformation and induction of microsatellite instability versus KRAS(G12V) induction of senescence markers in human colon cancer cells[J].Neoplasia,2009,11(11):1116-1131.
  • 7Duffy A,Kummar S.Targeting mitogen-activated protein kinase kinase (MEK) in solid tumors[J].Target Oncol,2009,4(4):267-273.
  • 8Wickenden J A,Jin H,Johnson M,et al.Colorectal cancer cells with the BRAF(V600E) mutation are addicted to the ERK1/2 pathway for growth factor-independent survival and repression of BIM[J].Oncogene,2008,27(57):7150-7161.
  • 9Ahlquist T,Bottillo I,Danielsen S A,et al.RAS signaling in colorectal carcinomas through alteration of RAS,RAF,NF1,and/or RASSF1A[J].Neoplasia,2008,10(7):680-686.
  • 10Makinen M J.Colorectal serrated adenocareinoma[J].Histopathology,2007,50(1):131-150.

同被引文献22

  • 1陶雅军,段世政,张明,刘君慧,吴怡潇,于慧,傅莹.649例大肠癌临床病理特征分析[J].实用肿瘤学杂志,2006,20(6):489-490. 被引量:5
  • 2尹德奎,张红春,马丽霞,齐玉华,岳丽荣.X线、内镜及超声联合应用在直乙肠交界处结肠癌诊断及分期中的价值[J].中国临床医学影像杂志,2007,18(4):296-297. 被引量:2
  • 3Bulun SE. Endometriosis [J]. N Engl J Med, 2009, 360 (3) :268-279.
  • 4Matsuzaki S, Canis M, Vaurs-Barriere C, et al. DNA mieroarray anal- ysis of gene expression profiles in deep endometriosis using laser capture microdissection [J]. Mol Hum Reprod, 2004, 10 (10): 719-728.
  • 5Chen Q, Zhang C, Chen Y, et al. Identification of endometriosis- related genes by representational difference analysis of cDNA [J]. Aust N Z J Obstet Gynaecol,2012,52(2) : 140-145.
  • 6Vinatier D, Orazi G, Cosson M, et al. Theories of endometriosis [J]. Eur J Obstet Gynecol Reprod Biol, 2001,96 (1):21-34.
  • 7Giudice LC, Kao LC. Endometriosis [J]. Lancet, 2004, 364 (9447) : 1789-1799.
  • 8Bukulmez O, Hardy DB, Carr BR, et al. Androstenedione up-regula- tion of endometrial aromatase expression via local conversion to es- trogen: potential relevance to the pathogenesis of endometriosis [J ]. J Clin Endocrinol Metab, 2008,93 (9) : 3471-3477.
  • 9Yoshino O, Osuga Y, Hirota Y, et al. Possible pathophysiological roles of mitogen-activated protein kinases (MAPKs) in endometrio- sis[J]. Am J Reprod Immunol,2004,52(5) :306-311.
  • 10Yamauchi N, Harada T, Taniguchi F, et al. Tumor necrosis factor- alpha induced the release of interleukin-6 from endometriotic stro- mal ceils by the nuclear factor-kappaB and mitogen activated pro- tein kinase pathways [J]. Fertil Steril, 2004, 82 (Suppl 3) : 1023-1028.

引证文献2

二级引证文献11

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