Jakupciak John P
National Institute of Standards & Technology, Biotechnology Division, 100 Bureau Drive, MS 8311, Gaithersburg, MD 20899, USA.
Expert Rev Mol Diagn. 2005 Sep;5(5):745-53. doi: 10.1586/14737159.5.5.745.
Since the hallmark report of the PCR-based telomeric repeat amplification protocol (TRAP) in 1994, there has been a flurry of investigations of telomerase activity on normal, benign, premalignant and cancerous samples representative of the various stages of tumorigenesis. Basic research and technological advances in human genetics, biochemistry and model systems have brought much progress towards the understanding of human infectious, hereditary and somatically acquired diseases. The knowledge of carcinogenesis has increased very rapidly in the past few years, particularly with the development of automated molecular biologic analysis of tumors and preneoplastic lesions. Despite the wide variety of studies on the potential use of telomerase as a cancer biomarker, the variability of reported telomerase activity and the lack of a transferable detection method have prevented it from becoming a routine clinical application. Real-time PCR is a clinically transferable method and the advancement of real-time measurements of telomerase will facilitate moving telomerase activity and technologies towards clinical validation. It is expected that the next 5 years will see telomerase integrated into the initial detection and follow-up monitoring of cancer patients. The hope is that the use of telomerase will finally translate into a diagnostic to help realize longer survival and a better quality of life.
自1994年基于聚合酶链反应(PCR)的端粒重复序列扩增 protocol(TRAP)标志性报告发表以来,针对代表肿瘤发生各个阶段的正常、良性、癌前和癌性样本的端粒酶活性展开了一系列研究。人类遗传学、生物化学和模型系统方面的基础研究与技术进步,在理解人类感染性、遗传性和体细胞获得性疾病方面取得了很大进展。在过去几年中,致癌作用的知识增长迅速,特别是随着肿瘤和癌前病变自动分子生物学分析的发展。尽管对端粒酶作为癌症生物标志物的潜在用途进行了广泛研究,但报告的端粒酶活性的变异性以及缺乏可转移的检测方法,使其未能成为常规临床应用。实时PCR是一种可临床转移的方法,端粒酶实时测量技术的进步将有助于推动端粒酶活性及相关技术走向临床验证。预计在未来5年内,端粒酶将被纳入癌症患者的初始检测和随访监测中。人们希望端粒酶的应用最终能转化为一种诊断方法,以帮助实现更长的生存期和更好的生活质量。