期刊文献+

甲状腺乳头状癌BRAF^(V600E)基因突变与钠碘同向转运体表达的研究 被引量:1

BRAF mutation and sodium iodide symporter expression in papillary thyroid cancer
原文传递
导出
摘要 目的:探讨甲状腺乳头状癌(PTC)患者中BRAFV600E基因突变及钠碘同向转运体(NIS)蛋白的表达及两者间的相关性。方法:收集2008-01-01-2011-01-01青岛大学医学院附属医院病理科PTC石蜡包埋组织30例,其中癌旁组织为正常组织(G正常组)15例,癌旁组织为结节性甲状腺肿组织(G结甲组)15例。对PTC组织行DNA提取、PCR扩增、基因测序检测BRAFV600E基因突变,同时采用免疫组化的方法分析NIS蛋白表达,结果以免疫组化评分(IHS)表示。结果:30例PTC均无BRAFV600E基因突变;30例PTC组织中NIS蛋白表达,从0~12分,G正常组IHS=(7.92±3.01)分,G结甲组IHS=(6.58±2.71)分,两组NIS差异无统计学意义,t=1.11,P=0.95;BRAFV600E突变与NIS蛋白表达无相关性。结论:尚未发现癌旁不同的PTCBRAFV600E基因有突变及NIS蛋白表达的差异。BRAFV600E基因突变与NIS表达在PTC中的关系有待进一步研究。 OBJECTIVE: To investigate the BRAF gene mutation, sodium iodide symporter(NIS) expression and the relationship between the two above genes in papillary thyroid caner (PTC) patients. METHODS: Thirty PTC patients durning January 1, 2008 and January 1, 2011 in our hospital were enrolled in this study. Including PTC 15 cases with the surrounding normal tissue (G normal) and another PTC 15 cases with the surrounding nodular goiter tissue (G NG). DNA was extracted from paraffin-embedded tumor specimens, and the presence of the BRAFV600Emutation was evaluated using PCR amplification and direct sequencing as well as tissue sections were subjected to immunohistochemistry (IH). RESULTS: There was no BRAFV600E gene mu tations while NIS protein were expressed differently in 30 PTC cases from 0 point to 12 points. The expression of NIS in G normal [IHS=(7. 92±3. 01) points] and G NG 〈IHS=(6.58±2.71) points] have no significant value (t=1. 11, P=0.95). There was no significant difference between BRAFV600E mutation and NIS expression in two groups. CONCLUSIONS: It's not found BRAFV600E mutation and NIS expression wariety in PTC with different surrounding tissue. The relationship of BRAFV600E mutation and NIS protein expression in papillary thyroid carcinoma need to be further studied.
出处 《中华肿瘤防治杂志》 CAS 北大核心 2012年第7期502-505,共4页 Chinese Journal of Cancer Prevention and Treatment
基金 国家自然科学基金(30970850)
关键词 甲状腺肿瘤 BRAF NIS 结节性甲状腺肿 papillary thyroid neoplasms BRAF NIS nodular goiter
  • 相关文献

参考文献16

  • 1Xing MZ. BRAF mutation in thyroid cancer[J]. Endocrine-Related Cancer,2005,12(2) :245-262.
  • 2Saito T, Endo T, Kawaguchi A, et al. Increased expression of the sodium/iodide symporter in papillary thyroid carcinomas[J]. J Clin Invest, 1998,101 (7): 1296-1300.
  • 3Dohan O, Baloch Z, Banrevi Z, et al. Rapid communication: predominant intraccllular overexpression of the Na(+)/1 (-) symporter (NIS) in a large sampling of thyroid cancer cases[J]. J Clin Endocrinol Metab, 2001,86(6).. 2697-2700.
  • 4Xing M, Weslra WH, Tufano RP, et al. BRAF mutation predicts a poorer clinical prognosis for papillary thyroid cancer[J]. J Clin Endecrinol Metab, 2005,90(12): 6373-6379.
  • 5Oler G,Cemtti JM. High prevalence of BRAF mutation in a Brazilian cohort of patients with sporadic papillary thyroid eareinomas[J]. Cancer, 2009,115(5) :972-980.
  • 6BarolloS, Pennelli G, Vianello F, et al. BRAF in primary and recurrent papillary thyroid cancers: the relationship with (131)I and 2-[(18) F]fluoro-2-deoxy-D-glucose uptake ability[J]. Eur J Endocrinol, 2010,163(4) : 659-663.
  • 7Durante C,Puxeddn E,Feretti E, et al. BRAF Mutations in papillary thyroid carcinomas inhibit genes involved in iodine metabolism [J]. J Clin Endocrinol Metab,2007,92(7):2840-2843.
  • 8Soslow RA, Dannenberg AJ, Rush D, et al. COX-2 is expressed in humanpulmonary, colonic, andmammary tumors[J]. Cancer, 2000,89(12) :2637-2645.
  • 9Hundahl SA, Fleming ID, Fremgen AM, et al. A National Cancer Data Base report on 53,856 cases of thyroid carcinoma treated in the U. S. ,1985-1995[J]. Cancer, 1998, 83(12) :2638-2648.
  • 10Basolo F.,Torregrossa L, Giannini R, et al. Correlation between the BRAFV600E mutation and tumor invasiveness in papillary thyroid carcinomas sraaller than 20 millimeters: analysis of 1060 cases[J]. J Clin Endocrinol Metab, 2010, 95(9):4197-4205.

二级参考文献6

  • 1Smith RA, Salajegheh A, Weinstein S, et al. Correlation be- tween BRAF mutation and the clinicopathological parameters in papillary thyroid carcinoma with particular reference to follicular variant[J]. HumPathol, 2011,42(4):501-506.
  • 2Kwak JY, Kim EK, Chung WY, et al. Association of BRAFV600E mutation with poor clinical prognostic factors and US features in Ko- rean patients with papillary thyroid microcarcinoma[J]. Radiology 2009,253(3):854-860.
  • 3Duiardin F, Pages JC, Collin C, et al. BRAF V600E mutation in papillary thyroid carcinoma: prevalence and detection in fine needle aspiration specimens[J]. Ann Pathol, 2010,30(4) : 252- 262.
  • 4Riesco-Eizaquirre G, Gutierrez-Martiez P, Garcia-Cabezas M A,et al. The oncogene BRAF V600E is assciatted with a high risk of recurrence and less differentiated papillary thyroid carcinoma due to the impairmeat of Na^+/Ⅰ- turgeting to the membrane [J]. Endocr Relat Cancer, 2006,13(1):257-269.
  • 5Riesco-Eizaguirre G, Rodriguez I, De la Vieja A, et al. The BRAFV600E oncogene induces transforming growth factor beta secretion leading to sodium iodide symporter repression and in- creased malignancy in thyroid cancer [J]. Cancer Res, 2009, (69) :8317-8325.
  • 6张恒,朱精强,唐颖,李志辉,魏涛.NIS蛋白表达对甲状腺癌诊断及^(131)I疗效预测的相关性研究[J].中国普外基础与临床杂志,2007,14(5):554-559. 被引量:5

共引文献7

同被引文献12

  • 1孔灵玲,张国安,崔文,王旭,周建,侯森,张仁亚.甲状腺癌组织LSD1表达临床意义分析[J].中华肿瘤防治杂志,2013,20(2):118-120. 被引量:4
  • 2Blair LP,Cap J,Zou MR. Epigenetic regulation by lysine demethylase 5 (KDMS) enzymes in cancer[J].Cancers (Basel),2011,(1):13831404.
  • 3Christensen J,Agger K,Cloos PA. RBP2 belongs to a family of demethylases,specific for tri and dimethylated lysine 4 on histone 3[J].Ce11,2007,(6):10631076.
  • 4Zhao L,Liu JM,He XY. The changing clinical patterns of primarv hyperparathyroidism in chinese patients:data from 2000to 2010 in a single clinical center[J].{H}Journal of Clinical Endocrinology and Metabolism,2013,(2):721-728.
  • 5Li N,Du XL,Reitzel LR. Impact of enhanced detection on the increase in thyroid cancer incidence in the United States:review of incidence trends by socioeconomic status within the sur veillance,epidemiology,and end results registry,1980 2008[J].{H}THYROID,2013,(1):103110.
  • 6Husson O,Haak H,van Steenbergen LN. Rising incidence,no change in survival and decreasing mortality from thyroid canc er in The Netherlands since 1989[J].{H}Endocrine Related Cancer,2013,(2):263271.
  • 7Islam AB,Richter WF,Lopez Bigas N. Selective targeting of histone methylation[J].{H}CELL CYCLE,2011,(3):413-424.
  • 8Lim S,Metzger E,Schüle R. Epigenetic regulation of cancer growth by histone demethylases[J].{H}International Journal of Cancer,2010,(9):1991-1998.
  • 9Zeng J,Ge Z,Wang L. The histone demethylase RBP2 is over-expressed in gastric cancer and its inhibition triggers senescence of cancer cells[J].{H}GASTROENTEROLOGY,2010,(3):981-992.
  • 10Teng YC,Lee CF,Li YS. Histone demethylase RBP2 pro motes lung tumorigenesis and cancer metastasis[J].{H}CANCER RESEARCH,2013,(15):4711-4721.

引证文献1

二级引证文献4

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