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人类端粒酶逆转录酶启动子突变作为胶质瘤的预后生物标志物。

Human TERT promoter mutations as a prognostic biomarker in glioma.

机构信息

Centre for Circulating Tumour Cell Diagnostics and Research, Ingham Institute for Applied Medical Research, 1 Campbell St, Liverpool, NSW, 2170, Australia.

School of Medicine, Western Sydney University, Campbelltown, NSW, 2560, Australia.

出版信息

J Cancer Res Clin Oncol. 2021 Apr;147(4):1007-1017. doi: 10.1007/s00432-021-03536-3. Epub 2021 Feb 6.

Abstract

The TERT promoter (pTERT) mutations, C228T and C250T, play a significant role in malignant transformation by telomerase activation, oncogenesis and immortalisation of cells. C228T and C250T are emerging as important biomarkers in many cancers including glioblastoma multiforme (GBM), where the prevalence of these mutations is as high as 80%. Additionally, the rs2853669 single nucleotide polymorphism (SNP) may cooperate with these pTERT mutations in modulating progression and overall survival in GBM. Using liquid biopsies, pTERT mutations, C228T and C250T, and other clinically relevant biomarkers can be easily detected with high precision and sensitivity, facilitating longitudinal analysis throughout therapy and aid in cancer patient management.In this review, we explore the potential for pTERT mutation analysis, via liquid biopsy, for its potential use in personalised cancer therapy. We evaluate the relationship between pTERT mutations and other biomarkers as well as their potential clinical utility in early detection, prognostication, monitoring of cancer progress, with the main focus being on brain cancer.

摘要

TERT 启动子(pTERT)突变,C228T 和 C250T,通过端粒酶激活、致癌和细胞永生化在恶性转化中起重要作用。C228T 和 C250T 作为重要的生物标志物,在多种癌症中均有出现,包括多形性胶质母细胞瘤(GBM),其突变的发生率高达 80%。此外,rs2853669 单核苷酸多态性(SNP)可能与这些 pTERT 突变协同作用,调节 GBM 的进展和总体生存率。通过液体活检,可以高精度和高灵敏度地检测到 pTERT 突变、C228T 和 C250T 以及其他临床相关的生物标志物,便于在整个治疗过程中进行纵向分析,并有助于癌症患者的管理。在这篇综述中,我们探讨了通过液体活检进行 pTERT 突变分析在个性化癌症治疗中的潜在用途。我们评估了 pTERT 突变与其他生物标志物之间的关系及其在早期检测、预后、癌症进展监测中的潜在临床应用,重点是脑癌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e6b/11801969/e9379a22d525/432_2021_3536_Fig1_HTML.jpg

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