首页> 外文期刊>Journal of research in medical sciences : >COMPARISON OF TELOMERASE ACTIVITY IN PROSTATE CANCER, PROSTATIC INTRAEPITHELIAL NEOPLASIA AND BENIGN PROSTATIC HYPERPLASIA
【24h】

COMPARISON OF TELOMERASE ACTIVITY IN PROSTATE CANCER, PROSTATIC INTRAEPITHELIAL NEOPLASIA AND BENIGN PROSTATIC HYPERPLASIA

机译:前列腺癌,前列腺上皮内淋巴瘤和良性前列腺增生症中端粒酶活性的比较

获取原文
           

摘要

BACKGROUND: Telomerase is a reverse transcriptase enzyme that synthesizes telomeric DNA on chromosome ends. The enzyme is important for the immortalization of cancer cells because it maintains the telomeres. METHODS: Telomerase activity (TA) was measured by fluorescence-based telomeric repeat amplification protocol (FTRAP) assay in prostate carcinoma and benign prostatic hyperplasia (BPH). RESULTS: TA was present in 91.4% of 70 prostate cancers, 68.8% of 16 prostatic intraepithelial neoplasia (PIN), 43.3% of 30 BPH*, 21.4% of 14 atrophy and 20% of 15 normal samples adjacent to tumor. There was not any significant correlation between TA, histopathological tumor stage or gleason score. In contrast to high TA in the BPH* tissue from the cancer-bearing gland, only 6.3% of 32 BPH specimens from patients only diagnosed with BPH were telomerase activity- positive. CONCLUSIONS: These results indicate that TA is present in most prostate cancers. The high rate of TA in tissue adjacent to tumor may be attributed either to early molecular alteration of cancer that was histologically unapparent, or to the presence of occult cancer cells. Our findings suggest that the re-expression of telomerase activity could be one step in the transformation of BPH to PIN.
机译:背景:端粒酶是一种逆转录酶,可在染色体末端合成端粒DNA。该酶对于癌细胞的永生化非常重要,因为它可以维持端粒。方法:采用基于荧光的端粒重复扩增方案(FTRAP)测定前列腺癌和良性前列腺增生(BPH)的端粒酶活性(TA)。结果:在70例前列腺癌中,TA占91.4%,在16例前列腺上皮内瘤变(PIN)中占68.8%,在30个BPH *中占43.3%,在14个萎缩中占21.4%,在与肿瘤相邻的15例正常样品中占20%。 TA,组织病理学肿瘤分期或格里森评分之间无显着相关性。与来自癌症腺体的BPH *组织中的高TA相比,在仅被诊断为BPH的患者的32个BPH标本中,只有6.3%的端粒酶活性为阳性。结论:这些结果表明TA存在于大多数前列腺癌中。与肿瘤相邻的组织中TA的高发生率可能归因于组织学上不明显的癌症的早期分子改变,也可能归因于隐匿性癌细胞的存在。我们的发现表明端粒酶活性的重新表达可能是BPH向PIN转化的第一步。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号