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Review
. 2022 Nov;12(11):e1111.
doi: 10.1002/ctm2.1111.

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

Affiliations
Review

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

Xiaotian Yuan et al. Clin Transl Med. 2022 Nov.

Abstract

Background: Telomerase 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.

Methods: The 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.

Conclusion: Mechanistic 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.

Keywords: TERT; TERT promoter mutations; cancer biomarker; telomerase; thyroid carcinoma; thyroid nodule.

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Conflict of interest statement

The authors declare that they have no conflict of interest.

Figures

FIGURE 1
FIGURE 1
The schematics of the telomerase complex and telomerase‐mediated telomere‐lengthening. Telomerase as an RNA‐dependent DNA polymerase is composed of telomerase reverse transcriptase (TERT), non‐coding RNA template (TERC) and accessory proteins or co‐factors. TERT binds to TERC to form the telomerase core holoenzyme that synthesizes telomeric TTAGGG repeats using TERC‐containing CUAAC sequences as a template. TERT is also directly associated with N‐acetyltransferase number 10 (NAT10), and their interaction enhances enzymatic activity. TERC stably binds to the dyskerin complex consisting of dyskeratosis congenita 1 (DKC1), NOP10, NHP2 and GAR1; and the dyskerin complex is required for TERC stability. TERC also binds telomerase Cajal body protein 1 (TCAB1), the factor responsible for telomerase trafficking, assembling and function.
FIGURE 2
FIGURE 2
telomerase reverse transcriptase (TERT) promoter mutations and methylation for telomerase activation in thyroid carcinomas (TCs). (A) Frequencies of TERT promoter mutations (C228T and C250T) and association with cell differentiation and aggressiveness across four subtypes of TCs (see Refs. [11, 15] for details). PTC and FTC belong to differentiated thyroid carcinomas (DTCs), whereas poorly differentiated thyroid carcinoma (PDTC) and ATC are poorly differentiated and undifferentiated tumours, respectively. On the other hand, PDTC and ATC are the most aggressive TCs with the highest frequency of TERT promoter mutations. (B) The TERT promoter mutations (C228T or C250T), occurring in subsets of TCs, create a de novo ETS binding motif, and the GABPA‐GABPB1 complex binds this site, thereby activating TERT transcription and telomerase. On the other hand, oncogenic events result in the featured TC methylation pattern: Hypermethylation in the TERT promoter upstream of transcription starts site (UTSS, between 1295 800 and 1295 587 in Chr5), whereas hypomethylation in the transcription starts site (TSS, between 1295 363 and 1294 945) region. Of note, the TSS region is the proximal TERT promoter where two hotspot mutations take place. (C) TC and other malignant cells may exhibit monoallelic or biallelic TERT transcription. In cells with a monoallelic TERT expression, the expressing‐allele is characterized by the hypermethylated UTSS and hypomethylated TSS profile, which leads to open chromatin for TERT transcription. In contrast, the non‐expressing‐allele lacks this methylation pattern coupled with a closed chromatin.
FIGURE 3
FIGURE 3
Telomere shortening‐mediated telomere position effect (TPE)/TPE over long distances (OLD) and metabolic alterations in thyroid carcinomas (TCs). Shorter telomere‐mediated TPE/TPE‐OLD. Long telomeres in normal thyrocytes form a telomere‐loop structure in the region near the telomerase reverse transcriptase (TERT) locus, resulting in a repressed TERT epigenetic state (left panel). Significant telomere shortening in TCs prevents the loop formation, thereby leading to opened chromatins, which allow the access to the TERT promoter by transcriptional activators and subsequent TERT transcription. ATF: activating transcription factor
FIGURE 4
FIGURE 4
An integrated approach for telomerase‐based thyroid carcinoma (TC) precision medicine. Individual telomerase or telomere biomarkers, as shown in most clinical studies, have demonstrated their usefulness in TC precision medicine, including diagnostics and prediction of transformation risk, recurrence, metastasis and outcomes. It is conceivable that integrated analyses of all these telomerase/telomere‐related biomarkers may be more helpful. Moreover, the assay and evaluation system standardization of these biomarkers are required to establish a telomerase/telomerase reverse transcriptase (TERT)‐based molecular classification of TCs, which, together with the WHO classification, is expected to greatly improve TC care. In addition, the assay may also help identify TC patients suitable for telomerase/telomere‐based therapy, for instance, converting the mutated TERT promoter into a WT one in ATCs, and applying GRN163L to patients with TERT‐expressing PTCs and FTCs.

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