Evidence map›Paper›PMID 35996174›Full record

ArticleCancer cell international2022

Evolution of intra-tumoral heterogeneity across different pathological stages in papillary thyroid carcinoma.

Ornella Affinito, Francesca Maria Orlandella, Neila Luciano, Marco Salvatore, Giuliana Salvatore, Monica Franzese

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
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  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Presumed Pathogenic Germ Line and Somatic Variants in African American Thyroid Cancer.Thyroid : official journal of the American Thyroid Association · 2024
    Article
  11. Article
  12. Review
  13. Review
  14. Deep Learning Prediction ofMedicina (Kaunas, Lithuania) · 2023
    Article
  15. Article
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

6 authors at 4 institutions in 2 countries.

Ornella AffinitoIRCCS Synlab SDN S.P.A., Via Gianturco 113, 80143, Naples, Italy. ornella.affinito@synlab.it.
Francesca Maria OrlandellaDipartimento di Scienze Motorie e del Benessere, Università Degli Studi di Napoli Parthenope, Naples, Italy.
Neila LucianoDipartimento di Scienze Biomediche Avanzate, Università Degli Studi di Napoli "Federico II", Naples, Italy.
Marco SalvatoreIRCCS Synlab SDN S.P.A., Via Gianturco 113, 80143, Naples, Italy.
Giuliana Salvatore *Dipartimento di Scienze Motorie e del Benessere, Università Degli Studi di Napoli Parthenope, Naples, Italy.
Monica Franzese *IRCCS Synlab SDN S.P.A., Via Gianturco 113, 80143, Naples, Italy.
Ceinge Biotecnologie Avanzate (Italy) · ITParthenope University of Naples · ITSynlab Czech (Czechia) · CZUniversity of Naples Federico II · IT

Funding

Ministero dell'Istruzione, dell'Università e della Ricerca, Progetti di Ricerca di Rilevante Interesse Nazionale (PRIN) 2017MHJJ55
6 · The paper itself

Abstract

backgroundIntra-tumor heterogeneity (ITH) results from the continuous accumulation of mutations during disease progression, thus impacting patients' clinical outcome. How the ITH evolves across papillary thyroid carcinoma (PTC) different tumor stages is lacking.

methodsWe used the whole-exome sequencing data from The Cancer Genome Atlas Thyroid Cancer (TCGA-THCA) cohort to track the ITH and assessed its relationship with clinical features through different stages of the PTC progression. We further assayed the expression levels of the specific genes in papillary thyroid cancer cell lines compared to an immortalized normal thyroid epithelial cell line by qRT-PCR.

resultsWe revealed the timing of mutational processes and the dynamics of the temporal acquisition of somatic events during the lifetime of the PTC. ITH significantly influences the PTC patient's survival rate and, as genetic heterogeneity increases, the prognosis gets worse in advanced tumor stages. ITH also affects the mutational architecture of each clinical stage which is subject to periodic fluctuations. Different mutational processes may cooperate to shape a stage-specific mutational spectrum during the progression from early to advanced tumor stages. Moreover, different evolutionary paths characterize PTC progression across pathological stages due to both mutations recurrently occurring in all stages in hotspot positions and distinct codon changes dominating in different stages. A different expression level of specific genes also exists in different thyroid cancer cell lines.

conclusionsOur findings suggest ITH as a potential unfavorable prognostic factor in PTC and highlight the dynamic changes in different clinical stages of PTC, providing some clues for the precision medicine and suggesting different diagnostic decisions depending on the clinical stages of patients. Finally, complete clear guidelines to define risk stratification of PTC patients are lacking; thus, this work could contribute to defining patients who need more aggressive treatments and, in turn, could reduce the social burden of this cancer.

Indexed as

Mutational signaturesPapillary thyroid cancerPrognosisTCGA-THCATumor heterogeneityTumor stages

Identifiers

PMID35996174
PMCPMC9394008
OpenAlexW4292554244

What OpenQuestion holds

Textmetadata
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.