Evidence map›Paper›PMID 33260544›Full record

ArticleNanomaterials (Basel, Switzerland)2020

A Novel Nanoproteomic Approach for the Identification of Molecular Targets Associated with Thyroid Tumors.

María García-Vence, María Del Pilar Chantada-Vázquez, José Manuel Cameselle-Teijeiro, Susana B Bravo, Cristina Núñez

Open access · goldAbstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  7. Gold Nanoparticles Contact with Cancer Cell: A Brief Update.International journal of molecular sciences · 2022
    Review
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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

5 authors at 3 institutions in 1 country.

María García-VenceProteomic Unit, Instituto de Investigaciones Sanitarias, Complejo Hospitalario Universitario de Santiago de Compostela (IDIS-CHUS), 15706 Santiago de Compostela, Spain.
María Del Pilar Chantada-VázquezProteomic Unit, Instituto de Investigaciones Sanitarias, Complejo Hospitalario Universitario de Santiago de Compostela (IDIS-CHUS), 15706 Santiago de Compostela, Spain.
José Manuel Cameselle-TeijeiroDepartment of Anatomic Pathology, Clinical University Hospital, Instituto de Investigación Sanitaria (IDIS), Galician Healthcare Service (SERGAS), 15703 Santiago de Compostela, Spain.ORCID 0000-0002-5516-8914
Susana B BravoProteomic Unit, Instituto de Investigaciones Sanitarias, Complejo Hospitalario Universitario de Santiago de Compostela (IDIS-CHUS), 15706 Santiago de Compostela, Spain.ORCID 0000-0001-7615-3079
Cristina NúñezResearch Unit, Hospital Universitario Lucus Augusti (HULA), Servizo Galego de Saúde (SERGAS), 27002 Lugo, Spain.ORCID 0000-0003-1554-9891
Complejo Hospitalario Universitario de Santiago · ESHospital Universitario Lucus Augusti · ESUniversidade de Santiago de Compostela · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A thyroid nodule is the most common presentation of thyroid cancer; thus, it is extremely important to differentiate benign from malignant nodules. Within malignant lesions, classification of a thyroid tumor is the primary step in the assessment of the prognosis and selection of treatment. Currently, fine-needle aspiration biopsy (FNAB) is the preoperative test most commonly used for the initial thyroid nodule diagnosis. However, due to some limitations of FNAB, different high-throughput "omics" approaches have emerged that could further support diagnosis based on histopathological patterns. In the present work, formalin-fixed paraffin-embedded (FFPE) tissue specimens from normal (non-neoplastic) thyroid (normal controls (NCs)), benign tumors (follicular thyroid adenomas (FTAs)), and some common types of well-differentiated thyroid carcinoma (follicular thyroid carcinomas (FTCs), conventional or classical papillary thyroid carcinomas (CV-PTCs), and the follicular variant of papillary thyroid carcinomas (FV-PTCs)) were analyzed. For the first time, FFPE thyroid samples were deparaffinized using an easy, fast, and non-toxic method. Protein extracts from thyroid tissue samples were analyzed using a nanoparticle-assisted proteomics approach combined with shotgun LC-MS/MS. The differentially regulated proteins found to be specific for the FTA, FTC, CV-PTC, and FV-PTC subtypes were analyzed with the bioinformatic tools STRING and PANTHER showing a profile of proteins implicated in the thyroid cancer metabolic reprogramming, cancer progression, and metastasis. These proteins represent a new source of potential molecular targets related to thyroid tumors.

Indexed as

gold nanoparticles (AuNPs)magnetic nanoparticles (FeNPs)molecular targetprotein corona (PC)silver nanoparticles (AgNPs)thyroid cancer

Identifiers

PMID33260544
PMCPMC7761166
OpenAlexW3108658613

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.