期刊文献+

抑癌基因FHIT和WWOX在胃腺癌中的表达及其临床意义 被引量:2

The Expression of Tumor Suppressor Genes FHIT and WWOX in Gastric Carcinoma and Its Clinical Significance
原文传递
导出
摘要 目的通过检测FHIT蛋白和WWOX蛋白在胃腺癌组织中表达情况和FHITmRNA和WWOXmRNA在胃腺癌和癌旁正常组织的表达情况,分析两者与临床病理特征之间的关系及两者之间是否具有相关性。方法随机抽取佳木斯大学附属第一医院普外科2000年到2011年期间的70例胃腺癌切除组织标本,采用免疫组化和RT-PCR方法检测胃腺癌组织中临床病理关系及胃腺癌与癌旁正常组织(距肿瘤边缘>5CM)的关系。结果 (1)FHIT和WWOX均阳性表达28例。FHIT和WWOX均阴性表达24例。FHIT阳性而WWOX阴性8例。FHIT阴性而WWOX阳性10例。FHIT和WWOX在胃腺癌中的表达成正相关性。(2)FHITmRNA与WWOXmRNA在70例胃腺癌组织中表达较癌旁组织低者分别有22例和28例;较癌旁胃正常组织高者均有6例。FHITmRNA和WWOXmRNA在胃腺癌的表达低于癌旁胃组织。结论 (1)FHIT和WWOX在胃腺癌组织中阳性表达率较低,在组织学分级,病理分期中呈正相关,而与年龄和病理分型无相关性。(2)FHIT和WWOX的在胃腺癌组织中与癌旁胃正常组织中差异有显著性。(3)FHITmRNA和WWOXmRNA在胃腺癌组织中的低表达呈低度正相关性。(4)FHIT和WWOX是重要的抑癌基因。 Objective Through detection of FHIT and WWOX protein in gastric adenocareinoma tissue expression level and the detection of FHITmRNA and WWOXmRNA in gastric carcinoma and adjacent normal tissue expression, analyzing the relationship between the two and the clinical and pathological characteristics, and whether they have any correlations. Methods Randomly select 70 cases of gastric cancer resected tissue specimen in general surgery from 2000 to 2011 in the first affiliated hospital of Jiamusi University, using immunohistochemical and RT - PCR method for the detec- tion of gastric adenocarcinoma in relation to clinicopathologic, as well as the relationship between gastric carcinoma and adjacent normal tissues (from the tumor margin 〉 5cm). Results 1. The FHIT and WWOX protein expression is positive ralated in gastric adenocareinoma. 2. In gastric adenocar- cinoma the FHIT and WWOX mRNA expression positive rate was significantly lower than the adjacent normal tissue. Conclusions 1. The positive ex- pression rate of FHIT and WWOX in gastric adenocarcinoma is low, and the histological grade, pathological stage is closely correlated while age and pathologic type have no correlation. 2. FHIT and WWOX were significantly different between gastric adenocarcinoma and gastric tissues of normal. 3. The low expression of FHIT and WWOX in gastric adenocarcinoma tissue are minuent positive related. 4. FHIT and WWOX are both important tumor suppressor genes.
出处 《中国病案》 2012年第10期72-73,共2页 Chinese Medical Record
基金 黑龙江省教育厅资助项目 编号:12521565
关键词 胃腺癌 脆性组氨酸三联体(FHIT) 含有氧化还原酶的WW结构域(WWOX)基因 免疫组织化学 RT—PCR Gastric adenocarcinoma FHIT WWOX Immunohistochemistry RT - PCR
  • 相关文献

参考文献8

  • 1吴孟超,吴在德.黄家驷外科学[M].北京:人民卫生出版社,2008:1832-1835.
  • 2朱兴国,孟翔凌,王成宏,王栋,胡闻,陈晓宇.p16蛋白、RUNX3蛋白在胃癌组织中的表达及其临床意义[J].安徽医科大学学报,2010,45(1):93-95. 被引量:9
  • 3Bednarek AK, Laflin KJ, Daniel RL, et al. WWOX, a novel WWdomain - containing prote in mapping to human chromosome16q23.3 - 24.1, a region frequently affected in breast cancer[ j].Cancer Res,2000,60 (8):2140-2145.
  • 4Otha M,Inoue H, Cotticelli MG,et al. The FHIT gene,spanningthe chromosome 3p 14.2 fragile site and renal carcinoma - asociat-ed t(3;'8) breakpoint, is abnormal in digestive tract cancers[ J].Cell, 1996,84 (4):587-597.
  • 5Zawacka - Pankau J, Ferens B. Enlightened protein: Fhit tumorsuppressor protein structure and function and its role in the toxici-ty of protoporphyrin IX - mediated photodynamic reaction [ j].Toxicol Appl Pharmacol,2009,241 (2) :246 - 252.
  • 6Bureke L, Khan MA, Freemann AN, et al. Alldic deletion analysisof the FHIT gene predicts poor survival in non small cell lung con-cert J]. Cancer Res,1998,58(12) :2533 - 2536.
  • 7Cantor JP, Liopoulos SD, Rao AS, et al. Epigeneticmodulation ofendogenous tumor suppressor expression in lung cancer xenograftssuppresses tumorigenicity[j]. Int J Cancer, 2007,120(1) : 24 -31.
  • 8Chang NS, Hsu LJ, Lin YS,et al. Oxidoreductase: A candidatetumor suppressor[ J] . Trends Mol Med, 2007, 13(1): 12 - 22.

二级参考文献7

  • 1王庆国,王峰,刘晶,王丹,丁相福.P16蛋白在胃癌组织中的异常表达及其意义[J].吉林大学学报(医学版),2005,31(6):921-923. 被引量:6
  • 2Hsu PI, Hsieh HL, Lee J, et al. Loss of RUNX3 expression correlates with differentiation, nodal metastasis, and poor prognosis of gastric cancer [ J ]. Ann Surg Oncol,2009,16 (6) :1686 -94.
  • 3Kishimoto I, Mitomi H, Ohkura Y,et al. Abnormal expression of p16( INK4a), cyclin D1, cyclin-dependent kinase 4 and retinoblastoma protein in gastric carcinomas [ J ]. J Surg Oncol, 2008,98 ( 1 ) :60 -6.
  • 4Ogasawara N, Tsukamoto T, Mizoshita T, et al. RUNX3 expression correlates with chief cell differentiation in human gastric cancers [ J ]. Histol Histopathol,2009,24 ( 1 ) : 31 - 40.
  • 5Honda T, Tamura G, Endoh Y,et al. Expression of tumor suppressor and tumor-related proteins in differentiated carcinoma, undifferentiated carcinoma with tubular component and pure undifferentiated carcinoma of the stomach [ J ]. Jpn J Clin Oncol,2005,35 (10) :580 -6.
  • 6陈金明,周海波,干建新,徐善祥,伍峻松,杨检新,周文,王沈华,易建华.胃癌RUNX3表达对凋亡与增殖细胞转换的影响及其预后价值[J].解剖学报,2008,39(4):543-546. 被引量:6
  • 7鲁文胜,汪渊.膀胱移性细胞癌p16基因缺失、突变、甲基化及其蛋白表达的研究[J].安徽医科大学学报,2004,39(1):18-18. 被引量:1

共引文献147

同被引文献15

  • 1谢思明,沈丽佳,殷操,阮萍,姚希.PTEN和FHIT在口腔鳞癌中的表达及意义[J].暨南大学学报(自然科学与医学版),2005,26(2):237-241. 被引量:6
  • 2BEDNAREK A K, LAFLIN K J, DANIEL RL, et al. WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3 -24.1, a region frequent- ly affected in breast cancer[ J 1. Cancer Es ,2000,60 (8) : 2140 - 2145.
  • 3OHTA M, INOUE H, COTTICELLI M G, et al. The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t ( 3 ; 8 ) breakpoint, is abnor- mal in digestive tract cancers [ J 1. Cell, 1996,84 (4) : 587 - 597.
  • 4CHEN X, LI P, YANG Z, et al. Expression of fragile his- tidine triad (FH1T) and WW-domain oxidoreductase gene (WWOX) in nasopharyngeal carcinoma[J]. Asian Pac J Cancer Prev, 2013,14( 1 ) :165 -71.
  • 5DINCER N, TEZEL G G, SUNGUR A, et al. Study of FHIT and WWOX expression in mucoepidermoid carcino- ma and adenoid cystic carcinoma of salivary gland [ J ]. Oral Onco1,2010,46 ( 3 ) : 195 - 199.
  • 6PIMENTA F J, GOMESD A, PERDIGAO P F, et al. Characterization of the tumor suppressor gene WWOX in primary human oral squamous cell carcinomas [ J 3. Int J Cancer, 2006, Mar 1 ;118(5) :1154 -8.
  • 7申洪.免疫组织化学显色反应强度定量理论、方法及应用解析[c]∥中国体视学学会.第十一届中国体视学与图像分析学术会议论文集,2006:25—33.
  • 8JAMSHIDIHA M, HABIBOLLAHI P, OSTAD S N, et al. Primary WWOX phosphorylation and JNK activation dur- ing etoposide induces eytotoxicity in HEK293 cells[J].Daru,2010,18(2) :141 - 145.
  • 9GOMES C C,DINIZ M G,OLIVEIRA C S,et al. Impact of WWOX alterations on p73, ANp73, p53, cell prolifera- tion and DNA ploidy in salivary gland neoplasms[J]. O- ral Dis, 2011,17 (6) :564 - 571.
  • 10刘文书,徐雅娟.FHIT在颊粘膜鳞癌组织中的表达及其临床意义[J].中国实验诊断学,2010,14(11):1775-1777. 被引量:2

引证文献2

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