期刊文献+

乳腺良恶性病变组织中ER、c-myc和hTERT的表达 被引量:1

Expression of ER, c-myc and hTERT in Benign and Malignant Breast Lesions
在线阅读 下载PDF
导出
摘要 [目的]探讨ER、c-myc和hTERT在乳腺良恶性病变组织中的表达及意义。[方法]用免疫组化SP法检测25例乳腺腺病和79例乳腺癌组织中ER、c-myc和hTERT的表达。[结果]ER、c-myc和hTERT在乳腺腺病组织中的阳性表达率分别为28.0%、12.0%和20.0%;在乳腺癌中的阳性率分别为72.2%、70.1%和92.4%,均明显高于乳腺腺病组,差异有显著性(P<0.01)。乳腺癌组中,c-myc和hTERT、ER和hTERT、ER和c-myc均呈显著正相关(r值分别为0.382、0.388和0.632,P<0.01),而hTERT和患者年龄、肿瘤大小(最大径)、淋巴结转移情况均无相关性(P>0.05)。[结论]在乳腺癌中ER、c-myc、hTERT均高表达,可能参与了乳腺癌的发生、发展,其中ER和c-myc的过表达可能和hTERT转录激活进而激活端粒酶有关。 [Purpose] To explore expression and significance of ER, c-myc and hTERT in benign and malignant breast lesions. [Methods] Expression of ER, c-myc and hTERT was detected by immunohistochemical method (SP method) in 25 cases with breast adenosis and 79 cases with breast carcinoma. [ Results ] The positive expression of ER, c-myc and hTERT in breast adenosis was 28.0%, 12.0% and 20.0% respectively; and that in breast carcinoma, 72.2%, 70.1% and 92.4% respectively, with significant difference between benign and malignancy(P〈0.01). Expressions between c-myc and hTERT; ER and hTERT; and ER and c-myc showed positive correlation (r=-0.382, 0.388 and 0.632 respectively, P〈0.01) in breast carcinoma; but the expression of hTERT was not correlated with age, tumor size and lymph node metastasis(P〉0.05) in breast carcinoma. [ Conclusion ] High expression of ER, c-myc and hTERT is found. The high expression may be involved in carcinogenesis and progress in breast carcinoma. High expression of ER and c-myc may correlate with transcription activation of hTERT and telomerase activation in carcinogenesis of breast cancer.
出处 《肿瘤学杂志》 CAS 2007年第1期50-52,共3页 Journal of Chinese Oncology
关键词 受体 雌激素 C-MYC 人端粒酶逆转录酶 端粒酶 乳腺疾病 乳腺肿瘤 receptors, estrogen c-myc human telomerase reverse transcriptase telomerase breast disease breast neoplasms
  • 相关文献

参考文献2

二级参考文献11

  • 1张静如.中国共产党与社会现代化[J].北京师范大学学报(社会科学版),1991(3):1-7. 被引量:14
  • 2[1]Ramakrishnan S,Eppenberger U,Mueller H,Shinkai Y,Narayanan R.Expression profile of the putative catalytic subunit of the telomerase gene.Cancer Res 1998;58:622-625
  • 3[2]Urquidi V,Tarin D,Goodison S.Role of telomerase in cell senescence and oncogenesis.Annu Rev Med 2000;51:65-79
  • 4[3]Meyerson M,Counter CM,Eaton EN,Ellisen LW,Steiner P,Caddle SD,Ziaugra L,Beijersbergen RL,Davidoff MJ,Liu Q,Bacchetti S,Haber DA,Weinberg RA.hEST2,the putative human telomerase catalytic subunit gene,is up-regulated in tumor cells and during immortalization.Cell 1997;90:785-795
  • 5[4]Shay JW,Bacchetti S.A survey of telomerase activity in human cancer.Eur J Cancer 1997;33:787-791
  • 6[5]Tang R,Cheng AJ,Wang JY,Wang TC.Close correlation between telomerase expression and adenomatous polyp progression in multistep colorectal carcinogenesis.Cancer Res 1998;58:4052-4054
  • 7[6]Weinrich SL,Pruzan R,Ma L,Ouellette M,Tesmer VM,Holt SE,Bodnar AG,Lichtsteiner S,Kim NW,Trager JB,Taylor RD,Carlos R,Andrews WH,Wright WE,Shay JW,Harley CB,Morin GB.Reconstitution of human telomerase with the template RNA component hTR and the catalytic protein subunit hTRT.Nat Genet 1997;17:498-502
  • 8[7]Beattie TL,Zhou W,Robinson MO,Harrington L.Reconstitution of human telomerase activity in vitro.Curr Biol 1998;8:177-180
  • 9[8]Nakayama J,Tahara H,Tahara E,Saito M,Ito K,Nakamura H,Nakanishi T,Tahara E,Ide T,Ishikawa F.Telomerase activation by hTRT in human normal fibroblasts and hepatocellular carcinomas.Nat Genet 1998;18:65-68
  • 10[9]Bodnar AG,Ouellette M,Frolkis M,Holt SE,Chiu CP,Morin GB,Harley CB,Shay JW,Lichtsteiner S,Wright WE.Extension of life-span by introduction of telomerase into normal human cells.Science 1998;279:349-352

共引文献46

同被引文献18

引证文献1

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