期刊文献+

PTEN和缺氧诱导因子-1α在大肠腺瘤一腺癌序列中的表达及意义 被引量:2

Expressions and Significance of PTEN,Hypoxia-inducible Factor-1 Alpha in Colorectal Adenoma-adenocarcinoma Sequence
在线阅读 下载PDF
导出
摘要 目的 :观察大肠腺瘤和腺癌组织中 PTEN、缺氧诱导因子 - 1α(HIF- 1α)表达情况 ,探讨两者在大肠腺瘤一腺癌序列发生发展中的作用及相互关系。方法 :采用原位杂交技术检测 18例大肠腺瘤和 6 2例大肠腺癌组织中 PTEN- m RNA、HIF-1αm RNA,用免疫组织化学 S- P方法检测 VEGF蛋白的表达。比较三者与大肠癌 Dukes分期、淋巴结转移、肝转移及组织学分级等病理特征的关系。结果 :18例大肠腺瘤 PTEN- m RNA、HIF- 1αm RNA、VEGF蛋白阳性表达率分别为 77.8% (14 / 18) ,38.9% (7/ 18) ,33.3% (6 / 18) ,大肠腺癌分别为 5 1.6 % (32 / 6 2 ) ,6 7.7% (42 / 6 2 ) ,5 9.7% (37/ 6 2 )。腺瘤组织 HIF- 1αm RNA、VEGF阳性表达率均低于腺癌细织 (P <0 .0 5 ) ,腺瘤组织 PTEN- m RNA阳性表达率显著高于腺癌组织 (P <0 .0 5 )。大肠腺癌细织中 PTEN- m RNA吸光值随 Dukes分期增高而逐渐降低 ,A期 (0 .1782± 0 .0 2 71) ,B期 (0 .15 38± 0 .0 397)分别与 C+D期(0 .14 70± 0 .0 5 2 4 )比较差异均具有显著性 (P <0 .0 5 )。 HIF- 1αm RNA、VEGF蛋白吸光值随 Dukes分期增高而逐渐升高 ,A期 ,HIF- 1α(0 .10 2 9± 0 .0 4 5 ) ,VEGF(0 .12 0 7± 0 .0 4 36 )分别与 B期 (0 .16 5 6± 0 .0 32 9、0 .15 72± 0 .0 5 Objective:To investigate the expressions and relationship of PTEN,hypoxia-inducible factor-1 alpha(HIF-1α ) in colorectal carcinogenesis.Methods:71 cases of formalin-fixed, paraffin-embedded colorectal neoplasms specimens (18 cases of adenomas, 62 cases of adenocarcinomas) were used. PTEN mRNA, HIF-1 α mRNA were detected by in situ hybridization. VEGF proteins were identified by citrate-microware SP immunohistochemical method.Results:The expressions of PTENmRNA, HIF-1 α mRNA, VEGF protein were detected in 14, 7,6 cases of 18 colorectal adenomas respectively. Significant difference was observed in positive rates of PTEN, HIF-1 a and VEGF expressions between colorectal adenomas and adenocarcinoma(P<0. 05).The levels of PTEN decreased as the pathologic stage increased. Reversely HIF-1 a and VEGF expressions increased with the specimen's dukes stage as follows: stage A(0. 1029±0. 045; 0. 1207±0. 0436), stage B(0. 1656±0. 0329;0. 1572±0. 0514), stage C+D (0. 2335±0. 0748;0. 2219±0. 0803). Significant differences of PTEN mRNA ,HIF-1α mRNA and VEGF were found between dukes stage A(0. 1782± 0.0271) and stage B(0.1538±0. 0397).The levels of PTEN in stage C+D were statically higher than stage A and B(P<0.05).HIF-1α and VEGF expressions correlated significantly with lymph node metastasis, liver metastasis and Duke' s stage. In colorectal carcinoma reduced levels of PTEN were statically significantly associated with increased expressions of HIF-1α mRNA (r s=-0.36,P<0.05) and VEGF protein (r s=-0.68, P<0.05) respectively. The levels of HIF-1 were correlated with VEGF expression (r s=0.71,P<0.01).Conclusion:The absence or low expression of PTEN and the increased levels of HIF-1α and VEGF may play an important role in carcinogenesis and progression of colorectal carci noma.
出处 《大肠肛门病外科杂志》 2004年第4期241-245,共5页 Journal of Coloproctological Surgery
基金 湖北省科技攻关项目 (编号 :2 0 0 3 AA3 0 1C0 3)
关键词 HIF-1α PTEN 大肠腺瘤 大肠腺癌 RNA VEGF蛋白 阳性表达率 DUKES分期 缺氧诱导因子-1Α 癌组织中 PTEN Hypoxia-inducible factor 1 alpha Vascular endothelial growth factor Colorectal tumor Gene
  • 相关文献

参考文献10

  • 1Guanti G, Resta N, Simone c, etal. Involvement of PTEN mutation in the genetic patway of colorectal cancerogensis, Hum. Mol. Genet,2000,9:283-287.
  • 2Hwang HP. Yi HK, Kim DS, etal. Suppression of tumorigenicity and metastasis in B16FIO cell by PTEN/MMC1/TEP1 gene. Cancer Letters,2001,172: 83-91.
  • 3Shin KH, Park JY, Park JG. PTEN gene mutations in colorectal cancers displaying microsatellite instability.Cancer Letters, 2001,174:189-194.
  • 4Jiang BH,Zheng JZ,Aoki M,et al. Phosphatidylinositol 3-kinase sigoaling mediates angiogenesis and expression of vascular endothelial growth factor in endothelial cells. Proc Natl Acad Sci USA,2000,4:1749-1753.
  • 5Zhong H,DeMarzo AM,Langhner E et al. Overexpression of hypoxia-inducible factor 1 in common human cancers and their metastasis. Cancer Res, 1999,59: 5830-5835.
  • 6Bir P,Schindl,Monika,Obermair A,et al. Overexpression of bypoxia-inducible factor is a marker for an unfavorable prognosis in early-stage invasive cervical cancer. Cancer Res,2000,60:4693-4696.
  • 7Bos R,Zhong H,Hanrahan CF,et al. Levels of hypooxiainducible factor 1 during breast carcinogenesis. J Natl Cancer Inst, 2001,93:309-313.
  • 8Folkman J, Watson K, Ingber D, ETAL. Inducation of angiogenesis during the transition from hypoerplasis to neoplasis. Nature, 1989,339:58-61.
  • 9江从庆,刘志苏,钱群,何跃明,袁玉峰,艾中立.大肠腺瘤和腺癌组织中缺氧诱导因子-1α的表达及其与VEGF、微血管密度的关系[J].癌症,2003,22(11):1170-1174. 被引量:30
  • 10江从庆海.缺氧诱导因子-1与肿瘤[J].国外医学(外科学分册),2001,28(6):327-330. 被引量:7

二级参考文献49

  • 1Kaio E, Tanaka S, Kitadai Y, et al. Clinical significance of angiogenic factor expression at the deepest invasive site of advanced colorectal carcinoma[J]. Oncology, 2003, 64(1): 61 -73.
  • 2Furndoi A, Tanaka S, Haruma K, et al. Clinical significance of vascular endothelial growth factor C expression and angiogenesis at the deepest invasive site of advanced coloreetal carcinoma[J]. Oncology, 2002, 82:157 - 166.
  • 3Zhong H, De Marzo AM, Laughner E, et al. Overexpression of hypoxia-inducible factor lalpha in common human cancers and their metastases[J]. Cancer Res, 1999,59:5830 - 5835.
  • 4Takahashi Y, Kitadai Y, Bucana CD, et al. Expression of vascular endothelial growth factor and its receptor, KDR, correlates with vascularity, metastasis, and proliferation of human colon cancer[J]. Cancer Res, 1995, 3964 -3968.
  • 5Weidner N. Intratumor microvessel density as a prognostic factor in cancer[J]. Am J Pathol, 1995, 147:9 - 19.
  • 6Wong MP, Cheung N, Yuen ST, et al. Vascular endothelial growth factor is up-regulated in the early pre-malignant stage of colorectal tumor progression[J]. In J Cancer, 1999, 81:845 -850.
  • 7Andre T. Kotelevets L, Vaillant JC, et al. Vegf, vegf-B, vegf-C and their receptors KDR, FLT-I and FLT-4 during the neoplastic progression of human colonic mucosa[J]. In J Cancer, 2000, 86:174 - 181.
  • 8Birner P, Schindl M, Obermair A, et al. Overexpression of hypoxia-inducible factor lalpha is a marker for an unfavorable prognosis in early-stage invasive cervical cancer[J]. Cancer Res, 2000, 60:4693 - 4696.
  • 9Bos R, Zhong H, Hanrahan CF, et al. Levels of hypoxiainducible factor-1 alpha during breast carcinogenesis[J]. J Natl Cancer Inst, 2001.93:309 - 313.
  • 10Folkman J, Watson K, Ingber D, et al. Inducation of angiogenesis during the transition from hyperplasia to neoplasis[J]. Nature, 1989, 339:58 - 61.

共引文献35

同被引文献20

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