期刊文献+

RAS基因家族在实体瘤中突变率的研究进展 被引量:3

Advances in research on mutation rate of RAS gene family in solid tumors
下载PDF
导出
摘要 RAS基因家族包含3种原癌基因,即KRAS、NRAS和HRAS。在多种肿瘤中RAS基因突变使其激活成为有致癌活性的癌基因。点突变、表达量升高以及插入/转位突变等是其常见的激活方式。深入了解RAS基因家族的突变特征以及其在各种肿瘤中的发生率,可以对肿瘤的发生、发展、早期诊断、靶向治疗以及预后起到很好的指导作用。本文分别从KRAS基因突变、NRAS基因突变以及HRAS基因突变3个方面,对RAS基因家族在实体瘤中突变率的研究进展进行文献回顾。 The RAS gene family contains three proto-oncogenes, namely KRAS, NRAS and HRAS. Mu- tations in a RAS gene in a variety of tumors activate it into an activated oncogene. Single point mutations, increased expression levels, and insertion/translocation mutations are common activation modes. A deep understanding of the mutation characteristics of the RAS gene family and its incidence in various tumors can play a good guiding role in tumor occurrence, development, early diagnosis, targeted therapy and prognosis. This paper gives a review of the literature on the mutation rate of RAS gene families in solid tumors from three aspects: KRAS gene mutation, NRAS gene mutation and HRAS gene mutation.
作者 杨麒巍 隋玉杰 杜珍武 张桂珍 YANG Qiwei;SUI Yujie;DU Zhenwu;ZHANG Guizhen(Second Hospital of Jilin University,Medical Research Center,Changchun 130041,China;Second Hospital of Jilin University,Orthopedics Institute,Changchun 130041,China;Changehun Tumor Hospital,Changchun 130012,China)
出处 《中国体视学与图像分析》 2018年第3期303-310,共8页 Chinese Journal of Stereology and Image Analysis
基金 吉林省教育厅项目(JJKH20170853KJ) 吉林省科技厅项目(20180520111JH) 国家自然科学基金(81702195) 吉林省精准医学分子诊断应用示范项目(2016-2018 NDRC) 吉林省卫计委项目(20180520125JH) 吉林大学白求恩青年基金项目(2015409)
关键词 KRAS基因 NRAS基因 HRAS基因 基因突变 肿瘤 综述 KRAS gene NRAS gene HRAS gene gene mutation solid tumor review
  • 相关文献

参考文献5

二级参考文献44

  • 1朱虔兮,边建超,沈强,汤洪伟,张宏伟,吴毅.遗传因素在乳头状甲状腺癌发生中的作用[J].中国预防医学杂志,2004,5(5):321-323. 被引量:10
  • 2顾华丽,田字彬.ras基因突变与肿瘤的关系[J].青岛大学医学院学报,2005,41(4):372-375. 被引量:14
  • 3Xiong H Q, Rosenberg A, LoBuglio A, et al. Cetuximab,a monoclonal antibody targeting the epidermal growth factor receptor, in combination with gemcitabine for advanced pancreatic cancer:a muhicenter phase H trial [J]. J Clin Oncol, 2004,22( 13 ) : 2610-2616. 被引量:1
  • 4Baselga J. Why the epidermal growth factor receptor? The rationale for cancer therapy [J]. Oncologist, 2002,7(Suppl 4): 2-8. 被引量:1
  • 5Doody J F, Wang Y, Pate1 S N, et al. Inhibitory activity of cetuximab on epidermal growth factor receptor mutations in non small cell lung cancers [J]. Mol Cancer Ther, 2007,6(10):2642-2651. 被引量:1
  • 6Van C E, Peeters M, Siena S, et al. Open-label phase Ⅲtrial of panitumumab plus best supportive care compared with best supportive care alone in patients with chemotherapy-refractory metastatic colo-rectal cancer [J]. J Clin Oncol, 2007, (25): 1658-1664. 被引量:1
  • 7Cohen E E, Rosen F, Stadler W M, et al. Phase Ⅱ trial of ZD1839 in recurrent or metastatic squamous cell carcinoma of the head and neck [J]. J Clin Oncol, 2003,21 (10):1980- 1987. 被引量:1
  • 8Polychronis A, Sinnett H D, Hadjiminas D, et al. Preoperative gefitinib versus gefitinib and anastrozole in postmenopausal patients with oestrogen-receptor positive and epidermal growth factor receptor positive primarybreast cancer: A double-blind placebo-controlled phase Ⅱ randomized trial [J]. Lancet Oneol, 2005,6(6) :383-391. 被引量:1
  • 9Xiong H Q, Rosenberg A, LoBuglio A, et al. Cetuximab,a monoclonal antibody targeting the epidermal growth factor receptor, in combination with gemcitabine for advanced pancreatic cancer:a muhicenter phase Ⅱ trial [J]. J Clin Oncal, 2004,22 (13) : 2610-2616. 被引量:1
  • 10Graeven U, Kremer B, Sudhoff T, et al. Phase I study of the humanised anti-EGFR monoclonal antibody matuzumab (EMD 72000) combined with gemcitabine in advanced pancreatic cancer [J]. Br J Cancer, 2006,94(9) : 1293-1299. 被引量:1

共引文献8

同被引文献19

引证文献3

二级引证文献12

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