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食管鳞状上皮癌变过程中p16与Fhit的表达及其意义 被引量:2

Expression and significance of p16 and Fhit protein in esophageal carcinoma patients
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摘要 目的探讨食管鳞状上皮癌变过程中p16与Fhit蛋白表达变化及其相互关系。方法采用免疫组化SP法对17例正常食管鳞状上皮、16例轻度不典型增生(Ⅰ级组)、16例中度不典型增生(Ⅱ级组)、17例重度不典型增生(Ⅲ级组)、10例原位癌、18例鳞状细胞癌组织中抑癌基因P16及Fhit的蛋白表达进行检测与分析。结果①从食管鳞状上皮→不典型增生→原位癌→鳞状细胞癌,随着食管病变的加重,p16及Fhit蛋白表达率呈逐渐降低趋势。②正常组除与不典型增生Ⅰ级组相比p16与Fhit蛋白表达差异无显著性(P>0.05)外,正常组与其余各组相比上述指标差异均有显著性(均为P<0.05);鳞状细胞癌组与不典型增生Ⅱ组、Ⅲ组、原位癌组相比p16与Fhit蛋白表达差异无显著性(P>0.05),鳞状细胞癌组与正常组、不典型增生Ⅰ级组比较上述指标差异均有显著性(P<0.05)。③p16与Fhit蛋白阳性表达率下降趋势一致。结论p16与Fhit蛋白表达的缺失在食管癌变过程的早期阶段就已经发生。p16与Fhit蛋白表达呈正相关,可能在食管上皮癌变过程中起到协同作用。 Objective To explore the expression changes of p16 and Fhit during esophageal carcinomatous development and the relationship between the two proteins. Methods p16 and Fhit protein expression was detected and analyzed in 17 cases of normal squamous epithelium, 16 cases of slight atypical hyperplasia (grade Ⅰ group ) , 16 eases of moderate atypical hyperplasia (grade Ⅱ group) , 17 cases of atypieal hyperplasia (grade Ⅲ group ) , 10 eases of carcinoma in situ, and 18 cases of esophageal squamous cell carcinoma by immunohistochemieal SP method. Results With advance of esophageal cancer,the expression rates of p16 and Fhit reduced gradually. There was not remarkable correlation in p16 and Fhit protein expression between normal group and grade Ⅰ group (P 〉 0.05 ) but there was signifieant difference among normal group and other groups ( P 〈 0.05 for each ). There was not significant difference in p16 and 1/hit expression among squamous cell carcinoma group and grade Ⅱ group, grade Ⅲ group and carcinoma in situ group (P 〉 0.05 ) but there was remarkable correlation in p16 and Fhit expression between squamous eell carcinoma group and normal group as well as grade 1 group ( P 〈 0.05 ). The positive expression rates of p16 and Fhit were similarly decreased. Conclusion The loss of p16 and Fhit protein expression occurs in the early stage of esophageal eareinomatous change, p16 is positively correlated with Fhit, which may play a synergistic role in the esophageal carcinoma.
出处 《中国综合临床》 北大核心 2006年第1期13-15,共3页 Clinical Medicine of China
基金 河北省自然基金课题(C2005000797) 河北省科技计划项目(032761100D1) 河北省重大攻关课题(03276198D)
关键词 食管鳞状细胞癌 P16 FHIT 蛋白表达 Esophageal squamous cell carcinoma P16 Fhit Protein expression
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参考文献9

  • 1Serrano M, Hannon G J, Beach D. A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4 [J]. Nature,1993,366(6 456) :704-707.
  • 2Ohta M,Incue H, Cotticelli MG,et al. The FHITgene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) break point, is abnormal in digestive tract cancers [ J ]. Cell,1996,84(4) :587-597.
  • 3Garinis GA, Gorgoulis VG, Mariatos G, et al. Association of allelic loss at the FHIT locus and p53 alterations with turnout kinetics and chromosomal instability in non-small cell lung carcinomas(NSCLCs) [J]. J Pathol,2001,193( 1 ) :55-65.
  • 4Ji L, Fang B, Yen N, et al. Induction of apoptosis and inhibition of tumorigenicity and tumor growth by adenovirus vector-mediated fragile histidine triad (FHIT) gene overexpression [ J ]. Cancer Res,1999,59(14) :3 333-3 339.
  • 5Mori M,Mimori K,Shiraishi T,et al. Altered expression of Fhit in carcinoma and precarcinomatous lesions of the esophagus[J]. Cancer Res,2000,60(5) :1 177-1 182.
  • 6李连弟,鲁凤珠,张思维,牧人,孙秀娣,皇甫小梅,孙杰,周有尚,欧阳宁慧,饶克勤,陈育德,孙爱明,薛志福,夏毅.中国恶性肿瘤死亡率20年变化趋势和近期预测分析[J].中华肿瘤杂志,1997,19(1):3-9. 被引量:869
  • 7蔡清萍,王强.FHIT基因的研究进展[J].国外医学(分子生物学分册),2002,24(2):70-73. 被引量:6
  • 8林亚华,叶巧滔.FHIT基因研究进展[J].国外医学(放射医学核医学分册),2001,25(6):275-279. 被引量:9
  • 9刘复生 RubioCA.早期食管癌及癌旁上皮的DNA分析[J].中华肿瘤杂志,1988,10(1):26-28.

二级参考文献39

  • 1[1]Ohta M et al. Cell,1996;84(4):587
  • 2[2]Kisielewski AE et al. Oncogene, 1998;17:83
  • 3[3]Sozzi G et al. Adv Cancer Res, 1998; 74: 141
  • 4[4]Nelson HH et al. Cancer Res,1998;58:1804
  • 5[5]Man S. Cancer Res,1996;56:3173
  • 6[6]Sard L et al. Proc Natl Acad Sci USA,1999;96:8489
  • 7[7]Yoshino K et al. Int J Cancer ,1998;76:176
  • 8[8]Sirashvili Z et al. Proc Natl Acad Sci USA, 1997; 94:13771
  • 9[9]Ji L et al. Cancer Res,1999;59:3333
  • 10[10]Otterson GA et al. J Natl Cancer Inst, 1998; 90:426

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