Evidence map›Paper›PMID 31278686›Full record

ArticleEndocrine2019

Differential expression of RET isoforms in normal thyroid tissues, papillary and medullary thyroid carcinomas.

Teresa Ramone, Cristina Romei, Raffaele Ciampi, Alessia Tacito, Paolo Piaggi, Liborio Torregrossa, Clara Ugolini, Rossella Elisei

Abstract read
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In one paragraph

Article in Endocrine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
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  4. HigherBiomolecules · 2021
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  5. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Teresa RamoneDepartment of Clinical and Experimental Medicine, Unit of Endocrinology University of Pisa, Pisa, Italy.
Cristina RomeiDepartment of Clinical and Experimental Medicine, Unit of Endocrinology University of Pisa, Pisa, Italy.ORCID 0000-0002-5957-8902
Raffaele CiampiDepartment of Clinical and Experimental Medicine, Unit of Endocrinology University of Pisa, Pisa, Italy.
Alessia TacitoDepartment of Clinical and Experimental Medicine, Unit of Endocrinology University of Pisa, Pisa, Italy.
Paolo PiaggiDepartment of Clinical and Experimental Medicine, Unit of Endocrinology University of Pisa, Pisa, Italy.
Liborio TorregrossaDepartment of Surgical and Medical Pathology, Unit of Pathology, University of Pisa, Pisa, Italy.
Clara UgoliniDepartment of Surgical and Medical Pathology, Unit of Pathology, University of Pisa, Pisa, Italy.
Rossella EliseiDepartment of Clinical and Experimental Medicine, Unit of Endocrinology University of Pisa, Pisa, Italy. rossella.elisei@med.unipi.it.
University of Pisa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

pourposesWe investigated the expression of RET9 and RET51 isoforms in medullary (MTC), papillary (PTC) thyroid carcinoma, normal thyroid tissues, and pheochromocytoma (PHEO) to verify if these isoforms are present also in follicular thyroid cell-derived tissues, and if there is a differential expression of RET9 and RET51 in MTC.

methodsNineteen patients with MTC, 18 patients with PTC, 18 samples of contralateral normal thyroid tissues, and 5 cases of PHEO were included in this study. RET isoform expression was studied by real-time RT-PCR.

resultsAll MTCs and PHEOs were positive for RET9 and RET51. Fourteen/eighteen (77.7%) PTC cases were positive for RET9 and/or RET51, and four were positive for only one of the genes. In normal thyroid tissues, 3/18 (16.7%) cases were negative for both isoforms, 4/18 (22.2%) were positive for both, and 11/18 (61.1%) were positive for only one. RET isoforms were expressed at different levels in MTC, PHEO, PTC, and normal thyroid tissues: RET9 expression was higher in PHEO than in MTC, PTC, and normal thyroid tissues. RET9 expression was also higher in MTC than in PTC and normal thyroid tissues. No difference was observed between PTC and normal thyroid tissues. A similar pattern of expression was observed for RET51. In addition, RET51 was significantly more expressed than RET9 in MTC, while RET9 was the predominant isoform in PHEO.

conclusionsOur study documented the expression of the RET9 and RET51 isoforms in normal thyroid and PTC tissues. RET9 and RET51 isoforms were also present in MTC and PHEO. RET51 expression was higher than RET9 expression in MTC, while there was no difference in the expression of these two isoforms in PTC and normal thyroid tissues. RET9 was more highly expressed than RET51 in PHEOs.

Indexed as

Adrenal Gland NeoplasmsAdultCarcinoma, NeuroendocrineCarcinoma, PapillaryFemaleGene Expression Regulation, NeoplasticHumansMaleMutationPheochromocytomaProtein IsoformsProto-Oncogene Proteins c-retThyroid GlandThyroid NeoplasmsProtein IsoformsProto-Oncogene Proteins c-retRET protein, humanIsoformsMedullary thyroid carcinomaNormal thyroidPapillary thyroid carcinomaRET

Identifiers

PMID31278686
OpenAlexW2954701897

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.