Yoshida Kazuhiro, Toge Tetsuya
Department of Surgical Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University.
Nihon Rinsho. 2004 Jul;62(7):1368-76.
Telomere ends are known to be shortened at every division of the cells. Telomerase is a ribonucleoprotein which compensate for the telomere ends and indispensable for the immortalization of the cells. It is reported that the enzyme is activated in a variety of cancer cells. In the present report, the enzyme was activated in more than 70% of gastrointestinal, bladder and breast cancer by TRAP assay. Moreover, in order to elucidate whether the enzyme activity is useful for the non-invasive detection of exfoliated cancer cells in the colon bowel washings, urine and fine needle aspirate of the breast tumors, TRAP assay was performed. In most of the cases, the positive findings were observed which support that the enzyme activity is useful for the clinical application. The expression of mRNA and protein for hTERT was detected in cancer cells, however, the assay contains the pitfall including the Taq inhibitor or telomerase inhibitor. Moreover, the activity is also detected although it is weak, in the benign or premalignant lesions. Further analysis is required for the clinical application of the method.
已知端粒末端在细胞每次分裂时都会缩短。端粒酶是一种核糖核蛋白,可补偿端粒末端,对细胞永生化不可或缺。据报道,该酶在多种癌细胞中被激活。在本报告中,通过端粒重复序列扩增法(TRAP 法)检测发现,超过 70%的胃肠道癌、膀胱癌和乳腺癌中该酶被激活。此外,为了阐明该酶活性是否有助于对结肠冲洗液、尿液及乳腺肿瘤细针穿刺抽吸物中脱落癌细胞进行无创检测,进行了端粒重复序列扩增法检测。在大多数病例中,观察到阳性结果,这支持该酶活性在临床应用中具有实用性。在癌细胞中检测到了人端粒酶逆转录酶(hTERT)的 mRNA 和蛋白表达,然而,该检测存在一些缺陷,包括 Taq 抑制剂或端粒酶抑制剂。此外,在良性或癌前病变中也检测到了该活性,尽管较弱。该方法的临床应用还需要进一步分析。