# TERT RNAscope analysis of sub-centimetric papillary thyroid carcinomas and synchronous lymph node metastases

**Authors:** Marie-Lisa Eich, Wiebke Jeske, Uschi Zenz, Costanza Chiapponi, Christina Alidousty, Sabine Merkelbach-Bruse, Reinhard Büttner, Anne M. Schultheis

PMC · DOI: 10.1186/s13044-024-00195-7 · Thyroid Research · 2024-04-15

## TL;DR

This study examines the role of TERT RNA in small thyroid cancers and their lymph node metastases, finding no TERT expression in metastases.

## Contribution

The study provides new evidence that TERT expression is not involved in early lymph node metastasis in small papillary thyroid carcinomas.

## Key findings

- TERT RNA expression was not detected in lymph node metastases using RNAScope®.
- Primary tumors and metastases showed low Ki-67 proliferation indices and wild-type p53 status.
- Morphological patterns were heterogeneous in both primary tumors and metastases.

## Abstract

Sub-centrimetric papillary thyroid carcinomas usually have a good prognosis with a cancer specific survival of > 99%, however in up to 65% of patients, lymph node metastases can be observed. Molecular alterations in BRAF, TERT and TP53 are associated with worse clinicopathological outcome in patients with papillary thyroid carcinoma.

Twenty-two cases of papillary thyroid carcinomas measuring ≤ 1 cm with synchronous lymph node metastases were examined regarding morphological patterns and immunohistochemical status of p53, Ki-67, and BRAF V600E status. TERT RNA expression in lymph node metastases were evaluated by RNAScope®.

Morphological patterns were heterogeneous in both primary tumors and lymph node metastases. Proliferation indices measured by Ki-67 were low. Both primary and lymph node metastases were wild type for p53 by immunohistochemical analysis. No lymph node metastasis showed TERT expression by RNAScope®.

Our data indicate that TERT expression is not involved in the development early lymph node metastasis in patients with sub-centimetric PTC.

The online version contains supplementary material available at 10.1186/s13044-024-00195-7.

## Linked entities

- **Genes:** BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673], TERT (telomerase reverse transcriptase) [NCBI Gene 7015], TP53 (tumor protein p53) [NCBI Gene 7157], TP53 (tumor protein p53) [NCBI Gene 7157]
- **Proteins:** Mki67 (antigen identified by monoclonal antibody Ki 67)
- **Diseases:** papillary thyroid carcinoma (MONDO:0005075)

## Full-text entities

- **Genes:** TERT (telomerase reverse transcriptase) [NCBI Gene 7015] {aka CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}
- **Diseases:** PTC (MESH:D000077273), lymph node metastases (MESH:D008207), cancer (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** V600E

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11017548/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC11017548/full.md

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Source: https://tomesphere.com/paper/PMC11017548