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Thyroid carcinoma-featured telomerase activation and telomere maintenance: Biology and translational/clinical significance

期刊

CLINICAL AND TRANSLATIONAL MEDICINE
卷 12, 期 11, 页码 -

出版社

JOHN WILEY & SONS LTD
DOI: 10.1002/ctm2.1111

关键词

cancer biomarker; telomerase; TERT; TERT promoter mutations; thyroid carcinoma; thyroid nodule

资金

  1. National Natural Science Foundation of China [82103492, 81972475]
  2. Shandong Provincial Natural Science Foundation [ZR2020MC063, ZR2020QH239, ZR2020QH245]
  3. Scientific Research Foundation of Qilu Hospital of Shandong University (Qingdao) [QDKY2019QN17]
  4. Key Research and Development Program of Shandong Province [2019GSF108140]
  5. Chinese Postdoctoral Science Foundation [2019T120593, 2018M630787]
  6. Swedish Cancer Society [19 0018 Pj]
  7. Swedish Research Council [2018-02993]
  8. Cancer Society in Stockholm [201393]
  9. Karolinska Institutet [2018-01524]

向作者/读者索取更多资源

This article summarizes the mechanisms of telomerase activation and TERT gene induction in thyroid carcinomas, as well as their implications in thyroid cancer precision medicine.
BackgroundTelomerase is a ribonucleoprotein complex consisting of a catalytic component telomerase reverse transcriptase (TERT), internal RNA template and other co-factors, and its essential function is to synthesize telomeric DNA, repetitive TTAGGG sequences at the termini of linear chromosomes. Telomerase is silent in normal human follicular thyroid cells, primarily due to the TERT gene being tightly repressed. During the development and progression of thyroid carcinomas (TCs), TERT induction and telomerase activation is in general required to maintain telomere length, thereby conferring TC cells with immortal and aggressive phenotypes. MethodsThe genomic alterations of the TERT loci including TERT promoter's gain-of-function mutations, copy number gain, fusion and rearrangements, have recently been identified in TCs as mechanisms to induce TERT expression and to activate telomerase. Importantly, numerous studies have consistently shown that TERT promoter mutations and TERT expression occur in all TC subtypes, and are robustly associated with TC malignancy, aggressiveness, treatment failure and poor outcomes. Therefore, the assessment of TERT promoter mutations and TERT expression is highly valuable in TC diagnostics, prognosis, treatment decision, and follow-up design. In addition, the TERT promoter is frequently hypermethylated in TC cells and tumors, which is required to activate TERT transcription and telomerase. Dysregulation of other components in the telomerase complex similarly upregulate telomerase. Moreover, shortened telomeres lead to altered gene expression and metabolism, thereby actively promoting TC aggressiveness. Here we summarize recent findings in TCs to provide the landscape of TC-featured telomere/telomerase biology and discuss underlying implications in TC precision medicine. ConclusionMechanistic insights into telomerase activation and TERT induction in TCs are important both biologically and clinically. The TERT gene aberration and expression-based molecular classification of TCs is proposed, and for such a purpose, the standardization of the assay and evaluation system is required. Moreover, the TERT-based system and 2022 WHO TC classification may be combined to improve TC care.

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